WO2015098660A1 - Liquid crystal composition and liquid crystal display element using same - Google Patents
Liquid crystal composition and liquid crystal display element using same Download PDFInfo
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- WO2015098660A1 WO2015098660A1 PCT/JP2014/083444 JP2014083444W WO2015098660A1 WO 2015098660 A1 WO2015098660 A1 WO 2015098660A1 JP 2014083444 W JP2014083444 W JP 2014083444W WO 2015098660 A1 WO2015098660 A1 WO 2015098660A1
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- 0 CC(F)=CC[C@](CC(*)C=C)C(*)=CC[C@@]1CCSCCC1 Chemical compound CC(F)=CC[C@](CC(*)C=C)C(*)=CC[C@@]1CCSCCC1 0.000 description 6
- IPKGILDIMGGFET-UHFFFAOYSA-N CC(CC1)CCC1c(cc1F)cc(F)c1F Chemical compound CC(CC1)CCC1c(cc1F)cc(F)c1F IPKGILDIMGGFET-UHFFFAOYSA-N 0.000 description 1
- AHFKXZIKTHTTBV-UHFFFAOYSA-N CC(CC1)CCC1c1cc(F)c(-c(cc2)cc(F)c2F)c(F)c1 Chemical compound CC(CC1)CCC1c1cc(F)c(-c(cc2)cc(F)c2F)c(F)c1 AHFKXZIKTHTTBV-UHFFFAOYSA-N 0.000 description 1
- MCWBDXJGUWGWFF-UHFFFAOYSA-N CCC(CC1)CCC1c(cc1)ccc1-c1ccc(-c(cc2F)cc(F)c2OC(F)(F)F)c(F)c1 Chemical compound CCC(CC1)CCC1c(cc1)ccc1-c1ccc(-c(cc2F)cc(F)c2OC(F)(F)F)c(F)c1 MCWBDXJGUWGWFF-UHFFFAOYSA-N 0.000 description 1
- MWZGKXXMRZKRDU-UHFFFAOYSA-N CCc(cc1)ccc1-c1cc(F)c(-c(cc2F)cc(F)c2F)c(F)c1 Chemical compound CCc(cc1)ccc1-c1cc(F)c(-c(cc2F)cc(F)c2F)c(F)c1 MWZGKXXMRZKRDU-UHFFFAOYSA-N 0.000 description 1
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- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
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- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/137—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering
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- C09K2019/0466—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group the linking chain being a -CF2O- chain
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- C09K19/3001—Cyclohexane rings
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- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
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Definitions
- the present invention relates to a nematic liquid crystal composition having a positive dielectric anisotropy ( ⁇ ) useful as a liquid crystal display material, and a liquid crystal display device using the same.
- Liquid crystal display elements are used in various measuring instruments, automobile panels, word processors, electronic notebooks, printers, computers, televisions, watches, advertisement display boards, etc., including clocks and calculators.
- Typical liquid crystal display methods include TN (twisted nematic) type, STN (super twisted nematic) type, vertical alignment type using TFT (thin film transistor), and IPS (in-plane switching) type.
- FFS far field switching
- the liquid crystal composition used in these liquid crystal display elements is stable against external stimuli such as moisture, air, heat, light, etc., and exhibits a liquid crystal phase in the widest possible temperature range centering on room temperature. And a low driving voltage is required.
- the liquid crystal composition is composed of several to several tens of kinds of compounds in order to optimize the dielectric anisotropy ( ⁇ ), the refractive index anisotropy ( ⁇ n) and the like for each display element.
- liquid crystal compositions exhibiting low voltage driving, high-speed response, and a wide operating temperature range in all driving methods such as vertical alignment (VA) type display as well as horizontal alignment type such as TN type, STN type, IPS type and FFS type. Things are sought.
- VA vertical alignment
- the liquid crystal display of the low power consumption model is due to the trend of reducing CO 2 emissions due to the consumption of fossil fuels causing global warming, which is also rushing to liquid crystal displays for TVs and in-vehicle use.
- the demand for devices has been increasing especially in recent years.
- the demand for low-power consumption LCD panels is increasing.
- Patent Document 2 there is a liquid crystal composition containing a compound containing —CH 2 CHFCF 2 O— linking group.
- Patent Document 1 is a composition showing a large dielectric anisotropy, paying attention to the fact that a large dielectric anisotropy in the composition contributes to a low threshold voltage, a small power consumption and a large contrast ratio in the device.
- the example of Patent Document 1 discloses a maximum ⁇ of 12.6 and the like.
- the —CF 2 O— linking group-containing compound and the —CH 2 CH 2 CF 2 O— linking group-containing compound have a problem that —CF 2 O— may be decomposed depending on the structure.
- the electric capacity of the panel driving portion determined by the sum of the electric capacity (C LC ) of the liquid crystal layer and the electric capacity (C ST ) on the TFT substrate side. Since the capacitance (C TOTAL ) becomes large, the charging time to the capacitor corresponding to C TOTAL is not negligible in the voltage writing scan to the TFT, which causes a rounding and delay of the voltage waveform, and as a display Phenomenon such as free car and deterioration of response speed were generated. Therefore, when the dielectric constant of the liquid crystal composition itself is high, it is necessary to suppress the capacitance (C ST ) on the TFT substrate side to a certain extent.
- a liquid crystal composition having a high dielectric constant is generally highly viscous, which is disadvantageous from the viewpoint of response speed. Therefore, as a means for improving the display quality and achieving a high-speed response, a method of reducing the capacitance of the liquid crystal layer, that is, a method using a liquid crystal composition having a very small ⁇ but a small ⁇ is considered. It has been confirmed that the composition has a low compatibility because most of the composition is composed of dielectrically neutral components, and the problem that the low-temperature storage stability that can withstand practical use cannot be ensured also arises.
- the liquid crystal composition according to the present invention and the liquid crystal display device using the same are liquid crystal compositions having a positive ⁇ , which suppresses / prevents a delay until the execution voltage is applied and is driven at a low voltage.
- Liquid crystal phase in a wider temperature range, low viscosity, good solubility at low temperature, high specific resistance, high voltage holding ratio, or stable against heat and light
- the present invention provides a composition, and further provides a liquid crystal display device exhibiting excellent display quality by suppressing display defects caused by image sticking or dripping marks, and using this liquid crystal composition.
- An object of the present invention is to provide a liquid crystal display device.
- the present invention is represented by the general formula (i):
- R i1 and R i2 each independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or an alkyl group having 1 to 10 carbon atoms.
- An alkoxy group, and at least one of R i1 and R i2 is an alkenyl group.
- liquid crystal composition having a relatively low dielectric anisotropy and a liquid crystal display element using the same, having low viscosity, high compatibility, or reduced deterioration due to heat and light. It becomes.
- the liquid crystal composition according to the present invention is useful for a liquid crystal display (for example, a TV or a car navigation system) in which a drive voltage can be set relatively high.
- the figure which shows typically an example of a structure of the liquid crystal display element of this invention The figure which shows typically an example of a structure of the liquid crystal display element of this invention.
- substrate 2 in FIG. 3 is a cross-sectional view of the liquid crystal display element shown in FIG.
- R i1 and R i2 each independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or an alkyl group having 1 to 10 carbon atoms.
- An alkoxy group, and at least one of R i1 and R i2 is an alkenyl group.
- the liquid crystal composition is as follows.
- the compound represented by the general formula (i) exhibits excellent compatibility when incorporated as a component of a liquid crystal composition having a dielectric anisotropy of greater than 0 and less than or equal to +5. It has been found that when one or more of the dielectrically neutral compounds represented by the formula (M-1) is contained in the composition, it exhibits higher compatibility.
- the combined use of the compound represented by the general formula (i) and the compound represented by the general formula (M-1) improves the parameters of various liquid crystal compositions related to improving the display quality of the liquid crystal display device.
- a high elastic constant, a high ⁇ n, and a low viscosity can be achieved, and the general formula (M-1) is large in the composition.
- a high elastic constant and extremely low viscosity can be achieved.
- the blending ratio of these general formulas (i) and (M-1) can be arbitrarily adjusted within a range that does not impair the compatibility of the liquid crystal composition as a whole. There is an effect of improving the transmittance and improving the response speed.
- the liquid crystal composition according to the present invention is preferably a p-type liquid crystal composition, and the dielectric anisotropy of the liquid crystal composition is preferably 5 or less, more preferably 4.5 or less, It is further preferably 4 or less, more preferably 3.5 or less, and particularly preferably 3 or less.
- the dielectric anisotropy is 5 or less, since the dielectric anisotropy is relatively low, the electric capacity (C LC ) of the liquid crystal layer can be kept low, and the voltage waveform in the voltage writing scan to the TFT. It is effective in suppressing phenomena such as free car and response speed deterioration caused by rounding and delay.
- the kind of the compound represented by the general formula (i) contained in the liquid crystal composition according to the present invention is, for example, one kind as one embodiment of the present invention.
- the content of the compound represented by the general formula (i) according to the present invention includes solubility at low temperature, transition temperature, electrical reliability, birefringence, process compatibility, dripping marks, image sticking, and different dielectric constants. It is necessary to appropriately adjust according to required performance such as directionality.
- the content (total) of the compound represented by the general formula (i) is preferably 1 to 35% by mass with respect to the total mass of the liquid crystal composition of the present invention. More preferable content is 1 to 32% by mass, 2 to 31% by mass, 3 to 30% by mass, 4 to 28% by mass, 5 to 26% by mass, and 6 to 25% by mass in this order.
- examples of the alkenyl group having 2 to 10 carbon atoms include a vinyl group, an allyl group, a 1-propenyl group, an isopropenyl group, a 2-butenyl group, 3 -Butenyl group, 1,3-butadienyl group, 2-pentenyl group, 3-pentenyl group, 2-hexenyl group and the like are mentioned, and linear or branched is preferable, and linear is more preferable.
- alkyl group having 1 to 10 carbon atoms examples include methyl group, ethyl group, propyl group, butyl group, isopropyl group, isobutyl group, t-butyl group, 3-pentyl group, isopentyl group.
- examples of alkyl groups are common and are appropriately selected from the above examples depending on the number of carbon atoms of each alkyl group.
- alkenyl group examples are common, and the alkenyl group having 2 to 10 carbon atoms according to the present invention is preferably linear or branched, and more preferably linear. More preferable alkenyl groups according to the present invention include the following formula (xi) (vinyl group), formula (xii) (1-propenyl group), formula (xiii) (3-butenyl group) and formula (xiv). ) (3-pentenyl group):
- alkyl group having 1 to 10 carbon atoms examples include methyl group, ethyl group, propyl group, butyl group, isopropyl group, isobutyl group, t-butyl group, 3- Examples include a pentyl group, an isopentyl group, a neopentyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, and a decyl group.
- alkyl groups are common and are appropriately selected from the above examples depending on the number of carbon atoms of each alkyl group.
- the alkyl group having 1 to 10 carbon atoms according to the present invention is preferably linear or branched, and more preferably linear.
- the compound represented by the general formula (i) is preferably, for example, a compound represented by the formula (i.1) to the formula (i.20), among which the formula (i.1), ( It is preferable that it is a compound represented by i.2), (i.5), (i.6), (i.11), (i.12).
- the type of the compound represented by the general formula (i) contained in the liquid crystal composition according to the present invention is, for example, one type as one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are one or two types. In another embodiment of the present invention, there are 1 to 3 types. Furthermore, in another embodiment of the present invention, there are 1 to 5 types. Furthermore, in another embodiment of the present invention, there are 2 to 5 types. Furthermore, in another embodiment of the present invention, there are 2 to 4 types. Furthermore, in another embodiment of the present invention, there are two to three types.
- the wide molecular weight distribution of the compound selected as a component of the liquid crystal composition is also effective for solubility, for example, one type of the compound represented by the formula (i.1) or (i.2), the formula (i .5) or (i.6), one kind from the compound represented by formula (i.11) or one from the compounds represented by formula (i.12), respectively, and combining these appropriately preferable.
- the compound represented by the general formula (i) according to the present invention preferably has a dielectric anisotropy at 25 ° C. of greater than ⁇ 2.0 and not more than +2.0, and has a dielectric anisotropy at 25 ° C. More preferably, the dielectric anisotropy at 25 ° C. is more than ⁇ 1.0 and +1.0 or less.
- the liquid crystal compound according to the present invention has the general formula (M-1):
- R 1 represents an alkenyl group having 1 to 10 carbon atoms
- R 2 represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a hydrogen atom, a fluorine atom, a cyano group, —CF 3 or Represents OCF 3
- Ring A and Ring B are each independently (A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and , (B) a 1,4-phenylene group (one —CH ⁇ present in this group or at least two non-adjacent —CH ⁇ may be replaced by —N ⁇ ),
- Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atom or a chlorine atom, n
- the capacitance of the liquid crystal layer is reduced, and the viscosity is low. It is possible to provide a liquid crystal composition exhibiting the action and effect of high compatibility (solubility) with the above compound.
- the electric capacity (C LC ) of the liquid crystal layer can be kept low, and free-cars caused by the rounding and delay of the voltage waveform in the voltage writing scan to the TFT It is effective in suppressing phenomena such as a deterioration in response speed.
- the compounds represented by the general formulas (i) and (M-1) exhibit high compatibility with other compounds having a dielectric anisotropy of +5.0 or more.
- the dielectric anisotropy at 25 ° C. is preferably more than ⁇ 2.0 and not more than +2.0, and the dielectric anisotropy at 25 ° C. More preferably, the property is more than ⁇ 1.5 and not more than +1.5, and the dielectric anisotropy at 25 ° C. is more preferably more than ⁇ 1.0 and not more than +1.0.
- the liquid crystal composition according to the present invention has a dielectric anisotropy at 25 ° C. of more than 0 and 5 or less, the electric capacity (C LC ) of the liquid crystal layer can be kept low, and the voltage in the voltage writing scan to the TFT can be reduced. It is effective in suppressing phenomena such as free car and response speed deterioration caused by waveform rounding and delay.
- the use of liquid crystal display elements has expanded, and there has been a significant change in the method of use and manufacturing method. In order to cope with these changes, it is required to optimize characteristics other than the basic physical property values as conventionally known.
- the method of injecting the liquid crystal composition into the substrate also changes, and the drop injection (ODF: One Drop Fill) method is the injection method from the conventional vacuum injection method. It has become mainstream.
- the problem that the drop marks when the liquid crystal composition is dropped on the substrate causes deterioration in display quality has been surfaced.
- the liquid crystal composition is less affected by, for example, a sudden pressure change or impact in the dropping device that occurs when the liquid crystal is dropped, and can be stably dropped over a long period of time. There is a need to be able to continue. Therefore, another object of the liquid crystal composition containing the compound represented by the general formula (i) and the compound represented by the general formula (M-1) is to solve such a problem.
- R 2 represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, and an alkoxy group having 1 to 10 carbon atoms. At least one selected from the group consisting of these is preferable, and at least one selected from the group consisting of an alkyl group having 1 to 10 carbon atoms and an alkenyl group having 2 to 10 carbon atoms is more preferable.
- n is preferably 1.
- ring A or ring B is preferably a phenyl group.
- the compound represented by the general formula (M-1) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (M-1-1), for example.
- R 1 represents an alkenyl group having 2 to 5 carbon atoms
- R 24 represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms. Represents.
- the content of the compound represented by the general formula (M-1-1) is low temperature solubility, transition temperature, electrical reliability, birefringence, process suitability, It is necessary to appropriately adjust according to required performance such as dripping marks, image sticking, high-speed response, and dielectric anisotropy.
- a preferable content of the compound represented by the general formula (M-1-1) is, for example, 0.01 to 50% by mass with respect to the total mass of the liquid crystal composition of the present invention. Is mentioned. Among these, for example, 0.05 to 45 mass%, 0.07 to 44 mass%, 0.1 to 42 mass%, 0.2 to 40 mass%, 0.5 to 38 mass%, 0.7 to 35% by mass or 1 to 33% by mass is preferred. In other embodiments, 1.5 to 28% by mass, 2 to 29% by mass, or 2.5 to 45% by mass, 3 to 40% by mass, 4 to 35% by mass, 5 to 25% by mass, 6 to 24 mass%, 7 to 45 mass%, 8 to 50 mass%, and 9 to 23 mass% are preferable.
- the compound represented by Formula (M-1-2) according to the present invention is preferably a compound represented by Formula (11.1) to Formula (11.9), for example.
- the types of compounds that can be combined are no particular restrictions on the types of compounds that can be combined, but they are combined according to the required performance, such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
- the formulas (11.1) and (11.2) are included in the liquid crystal composition, it contributes to the improvement of parameters relating to the high-speed response of the liquid crystal composition.
- the kind of compound to be used is one kind as one embodiment of this invention, for example. Or in another embodiment of the present invention, it is two or more types.
- the content of each compound represented by formula (11.1) is from 1% by mass to 55% by mass with respect to the total mass of the liquid crystal composition of the present invention. Is preferably 1% by mass or more and 35% by mass or less, and more preferably 1% by mass or more and 25% by mass or less. Among these, 1% by mass or more and 20% by mass or less, 2% by mass or more and 19% by mass or less, 3% by mass or more and 18% by mass or less, 3% by mass or more and 16% by mass or less, 4% by mass or more and 15% by mass or less. preferable.
- the content of each compound represented by formula (11.2) is from 1% by mass to 55% by mass with respect to the total mass of the liquid crystal composition of the present invention. Is preferably 1% by mass or more and 35% by mass or less, and more preferably 1% by mass or more and 25% by mass or less. Among these, 1% by mass or more and 20% by mass or less, 2% by mass or more and 19% by mass or less, 3% by mass or more and 18% by mass or less, 3% by mass or more and 16% by mass or less, 4% by mass or more and 15% by mass or less. preferable.
- the case where both the compound represented by the formula (11.1) and the compound represented by the formula (11.2) are contained is preferable from the viewpoint of compatibility.
- the preferred range of the total content of both compounds is the liquid crystal of the present invention. It is preferably 5% by mass to 35% by mass, preferably 6% by mass to 30% by mass, and preferably 7% by mass to 28% by mass with respect to the total mass of the composition. . In these, 8 mass% and 27 mass% or less, 9 mass% or more and 28 mass% or less, 10 mass% or more and 25 mass% or less are preferable.
- the liquid crystal composition according to the present invention includes at least one compound represented by the general formula (M-1), and there are no particular restrictions on the types of compounds that can be combined. They can be combined according to required performance such as temperature, electrical reliability, and birefringence.
- the kind of the compound represented by the general formula (i) or the general formula (M-1) contained in the liquid crystal composition according to the present invention is, for example, one kind as one embodiment of the present invention.
- there are 2 to 4 types Furthermore, in another embodiment of the present invention, there are two to three types.
- the content of the compound represented by the general formula (M-1) according to the present invention includes solubility at low temperature, transition temperature, electrical reliability, birefringence, process compatibility, drop marks, image sticking, dielectric It is necessary to appropriately adjust according to required performance such as rate anisotropy.
- the content (total) of the compound represented by the general formula (i) is preferably 1 to 50% by mass with respect to the total mass of the liquid crystal composition of the present invention. More preferable contents are 0.01 to 45% by mass, 0.05 to 42% by mass, 0.1 to 38% by mass, 0.7 to 35% by mass, 1 to 33% by mass, and 1.2 to 32%. It is preferable in order of mass%.
- the liquid crystal composition according to the present invention may further contain a compound represented by the following general formula (L) as an optional component, and the compound represented by the general formula (L) is a nonpolar compound (dielectric anisotropy). Is preferably -1.0 to +1.0).
- R L1 and R L2 each independently represents an alkyl group having 1 to 8 carbon atoms, and one or non-adjacent at least two —CH in the alkyl group.
- 2 — may be each independently substituted by —CH ⁇ CH—, —C ⁇ C—, —O—, —CO—, —COO— or —OCO—
- OL represents 0, 1, 2 or 3
- B L1 , B L2 and B L3 are each independently (A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and , (B) a 1,4-phenylene group (one —CH ⁇ present in this group or at least two non-adjacent —CH ⁇ may be replaced by —N ⁇ ),
- Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atoms
- the liquid crystal composition according to the present invention may contain one or more compounds represented by the general formula (L).
- L The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types. Furthermore, in another embodiment of this invention, they are five types. Furthermore, in another embodiment of the present invention, there are six types. Furthermore, in another embodiment of the present invention, there are seven types. Furthermore, in another embodiment of this invention, they are eight types. Furthermore, in another embodiment of the present invention, there are nine types.
- the compound represented by the general formula (L) is preferably contained in 1 to 15 types, and the compound represented by the general formula (L) is contained in 3 to 14 types. More preferably, the compound represented by the general formula (L) contains 5 to 12 types.
- the content of the compound represented by the general formula (L) includes solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, dripping marks, and burn-in. Therefore, it is necessary to appropriately adjust according to required performance such as dielectric anisotropy.
- the content of the compound represented by the general formula (L) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 20 to 98% by mass in one embodiment of the present invention. In still another embodiment of the present invention, the content is 30% to 90% by mass. In still another embodiment of the present invention, the content is 40% to 85% by mass. In still another embodiment of the present invention, the content is 45% to 85% by mass. In still another embodiment of the present invention, the content is 50% to 75% by mass. In still another embodiment of the present invention, the content is 55% to 70% by mass. In still another embodiment of the present invention, the content is 56% to 65% by mass. In still another embodiment of the present invention, the content is 25% to 85% by mass.
- the content is 30% to 80% by mass. In still another embodiment of the present invention, the content is 47% to 75% by mass. In still another embodiment of the present invention, the content is 53% to 70% by mass. In still another embodiment of the present invention, the content is 60% to 98% by mass. In still another embodiment of the present invention, the content is 62% to 95% by mass. In still another embodiment of the present invention, the content is 58% to 78% by mass. In still another embodiment of the present invention, the content is 65% to 85% by mass. In still another embodiment of the present invention, the content is 70% to 98% by mass. In still another embodiment of the present invention, the content is 47% to 97.5% by mass.
- the above lower limit value is preferably high and the upper limit value is preferably high. Furthermore, when the liquid crystal composition of the present invention maintains a high Tni and a liquid crystal composition with good temperature stability is required, the above lower limit value is preferably high and the upper limit value is high. Further, when it is desired to increase the dielectric anisotropy in order to keep the driving voltage low, it is preferable that the above lower limit value is lowered and the upper limit value is low.
- R L1 and R L2 are each a linear alkyl group having 1 to 5 carbon atoms or a linear alkyl group having 1 to 4 carbon atoms when the ring structure to which R L1 is bonded is a phenyl group (aromatic). (Or more) alkoxy groups and alkenyl groups having 4 to 5 carbon atoms are preferred, and when the ring structure to which they are bonded is a saturated ring structure such as cyclohexane, pyran and dioxane, linear carbon atoms An alkyl group having 1 to 5 carbon atoms, a linear alkoxy group having 1 to 4 (or more) carbon atoms, and a linear alkenyl group having 2 to 5 carbon atoms are preferable.
- the compound represented by the general formula (L) according to the present invention preferably has no chlorine atom in the molecule when chemical stability of the liquid crystal composition is required.
- the compound represented by the general formula (L) according to the present invention is preferably, for example, a compound selected from the compound group represented by the general formula (I).
- R 11 and R 12 each independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms.
- One or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, and the methylene group in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group May be substituted with an oxygen atom as long as the oxygen atoms are not continuously bonded, and may be substituted with a carbonyl group unless the carbonyl group is continuously bonded;
- a 11 and A 12 each independently represents a 1,4-cyclohexylene group, a 1,4-phenylene group, a 2-fluoro-1,4-phenylene group or a 3-fluoro-1,4-phenylene group.
- the solubility at low temperatures, viscosity, transition temperature, electrical reliability, birefringence, and the like are required. It is used in combination as appropriate according to the performance to be achieved.
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types. Furthermore, in another embodiment of this invention, they are four types. Furthermore, in another embodiment of this invention, they are five types. Furthermore, in another embodiment of this invention, they are six or more types.
- the content of the so-called bicyclic compound represented by the general formula (I) in the liquid crystal composition of the present invention is the solubility at low temperature, viscosity, transition temperature, electrical reliability, birefringence, process suitability. In addition, it is necessary to appropriately adjust according to required performance such as dripping marks, image sticking, and dielectric anisotropy.
- the content of the compound represented by the general formula (I) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 10 to 75% by mass in one embodiment of the present invention.
- the content is 10% to 70% by mass.
- the content is 10% to 65% by mass.
- the content is 10% to 60% by mass.
- the content is 15% to 60% by mass.
- the content is 15% to 59% by mass.
- the content is 15% to 56% by mass.
- the content is 15% to 52% by mass.
- the content is 15% to 51% by mass. In still another embodiment of the present invention, the content is 15% to 49% by mass. In still another embodiment of the present invention, the content is 15% to 48% by mass. In still another embodiment of the present invention, the content is 15% to 47% by mass. In still another embodiment of the present invention, the content is 15% to 45% by mass. In still another embodiment of the present invention, the content is 15% to 44% by mass. In still another embodiment of the present invention, the content is 15% to 43% by mass. In still another embodiment of the present invention, the content is 15% to 41% by mass. In still another embodiment of the present invention, the content is 15% to 39% by mass. In still another embodiment of the present invention, the content is 15% to 38% by mass.
- the content is 15% to 35% by mass. In still another embodiment of the present invention, the content is 15% to 33% by mass. In still another embodiment of the present invention, the content is 15% to 31% by mass. In still another embodiment of the present invention, the content is 15% to 30% by mass. In still another embodiment of the present invention, the content is 15% to 29% by mass. In still another embodiment of the present invention, the content is 15% to 28% by mass. In still another embodiment of the present invention, the content is 15% to 20% by mass. In still another embodiment of the present invention, the content is 17% to 60% by mass. In still another embodiment of the present invention, the content is 20% to 60% by mass. In still another embodiment of the present invention, the content is 27% to 60% by mass.
- the content is 28% to 60% by mass. In still another embodiment of the present invention, the content is 30% to 60% by mass. In still another embodiment of the present invention, the content is 31% to 60% by mass. In still another embodiment of the present invention, the content is 32% to 60% by mass. In still another embodiment of the present invention, the content is 33% to 60% by mass. In still another embodiment of the present invention, the content is 34% to 60% by mass. In still another embodiment of the present invention, the content is 35% to 60% by mass. In still another embodiment of the present invention, the content is 36% to 60% by mass. In still another embodiment of the present invention, the content is 37% to 60% by mass. In still another embodiment of the present invention, the content is 39% to 60% by mass.
- the content is 41% to 60% by mass. In still another embodiment of the present invention, the content is 42% to 60% by mass. In still another embodiment of the present invention, the content is 43% to 60% by mass. In still another embodiment of the present invention, the content is 44% to 60% by mass. In still another embodiment of the present invention, the content is 46% to 60% by mass. In still another embodiment of the present invention, the content is 47% to 60% by mass. In still another embodiment of the present invention, the content is 48% to 60% by mass. In still another embodiment of the present invention, the content is 49% to 60% by mass. In still another embodiment of the present invention, the content is 51% to 60% by mass. In still another embodiment of the present invention, the content is 17% to 45% by mass.
- the content is 27% to 29% by mass. In still another embodiment of the present invention, the content is 32% to 43% by mass. In still another embodiment of the present invention, the content is 34% to 38% by mass. In still another embodiment of the present invention, the content is 36% to 45% by mass. In still another embodiment of the present invention, the content is 37% to 48% by mass. In still another embodiment of the present invention, the content is 42% to 56% by mass. In still another embodiment of the present invention, the content is 43% to 52% by mass. In still another embodiment of the present invention, the content is 43% to 49% by mass. In still another embodiment of the present invention, the content is 43% to 44% by mass. In still another embodiment of the present invention, the content is 44% to 48% by mass. In still another embodiment of the present invention, the content is 47% to 51% by mass.
- the liquid crystal composition contains a compound group represented by the general formula (I) from the viewpoint of providing a liquid crystal composition having a low viscosity and a high response speed.
- the lower limit value of the content of the compound (group) represented by the general formula (I) is high and the upper limit value is high. High is preferred.
- the compound represented by the general formula (I) is preferably a compound selected from the group of compounds represented by the general formula (I-1).
- the compound represented by the general formula (I-1) is 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 2 to 9 It is preferable to contain 2 to 8 types, 2 to 6 types, 3 to 9 types, 3 to 7 types, 3 to 6 types, or 4 to 6 types mixed.
- the liquid crystal composition contains a compound group represented by the general formula (I-1) from the viewpoint of providing a liquid crystal composition having a low viscosity and a high response speed.
- the content of the compound represented by the general formula (I-1) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 10 to 70% by mass in one embodiment of the present invention.
- the content is 10% to 60% by mass.
- the content is 15% to 60% by mass.
- the content is 15% to 59% by mass.
- the content is 15% to 56% by mass.
- the content is 15% to 52% by mass.
- the content is 15% to 50% by mass.
- the content is 15% to 49% by mass.
- the content is 15% to 48% by mass. In still another embodiment of the present invention, the content is 15% to 47% by mass. In still another embodiment of the present invention, the content is 15% to 46% by mass. In still another embodiment of the present invention, the content is 15% to 45% by mass. In still another embodiment of the present invention, the content is 15% to 39% by mass. In still another embodiment of the present invention, the content is 15% to 38% by mass. In still another embodiment of the present invention, the content is 15% to 35% by mass. In still another embodiment of the present invention, the content is 15% to 33% by mass. In still another embodiment of the present invention, the content is 15% to 30% by mass. In still another embodiment of the present invention, the content is 15% to 28% by mass.
- the content is 15% to 26% by mass. In still another embodiment of the present invention, the content is 15% to 20% by mass. In still another embodiment of the present invention, the content is 17% to 60% by mass. In still another embodiment of the present invention, the content is 20% to 60% by mass. In still another embodiment of the present invention, the content is 21% to 60% by mass. In still another embodiment of the present invention, the content is 23% to 60% by mass. In still another embodiment of the present invention, the content is 26% to 60% by mass. In still another embodiment of the present invention, the content is 27% to 60% by mass. In still another embodiment of the present invention, the content is 2% to 60% by mass. In still another embodiment of the present invention, the content is 30% to 60% by mass.
- the content is 33% to 60% by mass. In still another embodiment of the present invention, the content is 34% to 60% by mass. In still another embodiment of the present invention, the content is 35% to 60% by mass. In still another embodiment of the present invention, the content is 36% to 60% by mass. In still another embodiment of the present invention, the content is 37% to 60% by mass. In still another embodiment of the present invention, the content is 38% to 60% by mass. In still another embodiment of the present invention, the content is 39% to 60% by mass. In still another embodiment of the present invention, the content is 42% to 60% by mass. In still another embodiment of the present invention, the content is 43% to 60% by mass. In still another embodiment of the present invention, the content is 46% to 60% by mass.
- the content is 47% to 60% by mass. In still another embodiment of the present invention, the content is 49% to 60% by mass. In still another embodiment of the present invention, the content is 50% to 60% by mass. In still another embodiment of the present invention, the content is 17% to 45% by mass. In still another embodiment of the present invention, the content is 21% to 24% by mass. In still another embodiment of the present invention, the content is 27% to 38% by mass. In still another embodiment of the present invention, the content is 28% to 29% by mass. In still another embodiment of the present invention, the content is 23% to 46% by mass. In still another embodiment of the present invention, the content is 34% to 38% by mass.
- the content is 36% to 45% by mass. In still another embodiment of the present invention, the content is 37% to 48% by mass. In still another embodiment of the present invention, the content is 42% to 48% by mass. In still another embodiment of the present invention, the content is 38% to 49% by mass. In still another embodiment of the present invention, the content is 42% to 56% by mass. In still another embodiment of the present invention, the content is 42% to 50% by mass. In another embodiment of the present invention, the content is 43 to 52% by mass. In another embodiment of the present invention, the content is 46 to 47% by mass.
- the above lower limit value is preferably high and the upper limit value is preferably high.
- the compound represented by the general formula (I-1) is preferably a compound selected from the group of compounds represented by the general formula (I-1-1).
- the liquid crystal composition according to the present invention particularly includes the compound group represented by the general formula (I-1-1) from the viewpoint of maintaining a low viscosity and providing a liquid crystal composition having a high response speed. preferable.
- the content of the compound represented by the general formula (I-1-1) is 1 to 45% by mass with respect to the total mass of the liquid crystal composition of the present invention. .
- the content is 1 to 35% by mass.
- the content is 1% to 30% by mass.
- the content is 1% to 26% by mass.
- the content is 1% to 21% by mass.
- the content is 1% to 16% by mass.
- the content is 1% to 15% by mass.
- the content is 1% to 13% by mass.
- the content is 1% to 12% by mass. In still another embodiment of the present invention, the content is 1% to 11% by mass. In still another embodiment of the present invention, the content is 1% to 10% by mass. In still another embodiment of the present invention, the content is 1% to 8% by mass. In still another embodiment of the present invention, the content is 1% to 7% by mass. In still another embodiment of the present invention, the content is 1% to 5% by mass. In still another embodiment of the present invention, the content is 1% to 4% by mass. In still another embodiment of the present invention, the content is 3% to 30% by mass. In still another embodiment of the present invention, the content is 4% to 30% by mass.
- the content is 5% to 30% by mass. In still another embodiment of the present invention, the content is 6% to 30% by mass. In still another embodiment of the present invention, the content is 7% to 30% by mass. In still another embodiment of the present invention, the content is 8% to 30% by mass. In still another embodiment of the present invention, the content is 9% to 30% by mass. In still another embodiment of the present invention, the content is 10% to 30% by mass. In still another embodiment of the present invention, the content is 11% to 30% by mass. In still another embodiment of the present invention, the content is 12% to 30% by mass. In still another embodiment of the present invention, the content is 13% to 30% by mass. In still another embodiment of the present invention, the content is 3% to 26% by mass.
- the content is 3% to 13% by mass. In still another embodiment of the present invention, the content is 3% to 8% by mass. In still another embodiment of the present invention, the content is 4% to 7% by mass. In still another embodiment of the present invention, the content is 5% to 12% by mass. In still another embodiment of the present invention, the content is 9% to 12% by mass. In still another embodiment of the present invention, the content is 6% to 16% by mass. In still another embodiment of the present invention, the content is 7% to 16% by mass. In still another embodiment of the present invention, the content is 7% to 10% by mass. In still another embodiment of the present invention, the content is 8% to 26% by mass.
- the content is 8% to 15% by mass. In still another embodiment of the present invention, the content is 8% to 13% by mass. In still another embodiment of the present invention, the content is 9% to 25% by mass. In still another embodiment of the present invention, the content is 10% to 21% by mass. In still another embodiment of the present invention, the content is 12% to 21% by mass. In still another embodiment of the present invention, the content is 13% to 16% by mass. In still another embodiment of the present invention, the content is 11% to 26% by mass.
- the compound represented by the general formula (I-1-1) is preferably a compound selected from the group of compounds represented by formula (1.1) to formula (1.5), 1.2) or a compound represented by formula (1.3) is preferred, and a compound represented by formula (1.3) is particularly preferred.
- the response is that the content of the compound represented by the formula (1.2) is high.
- the content of the compound represented by the formula (1.3) is effective in improving the speed, and the following range is preferable because a liquid crystal composition having a high response speed and high electrical and optical reliability can be obtained.
- the content of the compound represented by the formula (1.3) is, for example, 1 to 45% by mass in one embodiment of the present invention with respect to the total mass of the liquid crystal composition of the present invention.
- the content is 1 to 35% by mass.
- the content is 1% to 30% by mass.
- the content is 1% to 25% by mass.
- the content is 1% to 21% by mass.
- the content is 1% to 18% by mass.
- the content is 1% to 16% by mass.
- the content is 1% to 15% by mass. Alternatively, in another embodiment of the present invention, the content is 1% to 13% by mass. Alternatively, in another embodiment of the present invention, the content is 1% to 12% by mass. Alternatively, in another embodiment of the present invention, the content is 1% to 11% by mass. Alternatively, in another embodiment of the present invention, the content is 1% to 10% by mass. Alternatively, in another embodiment of the present invention, the content is 1% to 8% by mass. Alternatively, in another embodiment of the present invention, the content is 1% to 7% by mass. Alternatively, in another embodiment of the present invention, the content is 1% to 5% by mass.
- the content is 1% to 4% by mass. Alternatively, in another embodiment of the present invention, the content is 3% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 4% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 5% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 6% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 7% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 8% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 9% to 21% by mass.
- the content is 10% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 11% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 12% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 13% to 21% by mass. Alternatively, in another embodiment of the present invention, the content is 3% to 13% by mass. Alternatively, in another embodiment of the present invention, the content is 3% to 8% by mass. Alternatively, in another embodiment of the present invention, the content is 4% to 7% by mass. Alternatively, in another embodiment of the present invention, the content is 5% to 12% by mass.
- the content is 9% to 12% by mass.
- the content is 6% to 16% by mass.
- the content is 10% to 16% by mass.
- the content is 13% to 16% by mass.
- the content is 7% to 16% by mass.
- the content is 7% to 10% by mass.
- the content is 8% to 18% by mass.
- the content is 8% to 15% by mass.
- the content is 8% to 13% by mass.
- the content is 9% to 13% by mass.
- the compound represented by the general formula (I-1) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (I-1-2).
- R 12 has the same meaning as in general formula (I).
- the number of types of compounds used as the general formula (I-1-2) is, for example, one type as an embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types.
- the content of the compound represented by the general formula (I-1-2) is such that solubility at low temperature, viscosity, transition temperature, electrical reliability, birefringence, process suitability It is necessary to adjust appropriately according to required properties such as property, dripping marks, image sticking, and dielectric anisotropy.
- the content of the compound represented by the general formula (I-1-2) is 1 to 70% by mass with respect to the total mass of the liquid crystal composition of the present invention. .
- the content is 1 to 65% by mass.
- the content is 1 to 55% by mass.
- the content is 1% to 50% by mass.
- the content is 1% to 49% by mass.
- the content is 1% to 47% by mass.
- the content is 1% to 45% by mass.
- the content is 1% to 44% by mass.
- the content is 1% to 40% by mass. In still another embodiment of the present invention, the content is 1% to 39% by mass. In still another embodiment of the present invention, the content is 1% to 38% by mass. In still another embodiment of the present invention, the content is 1% to 36% by mass. In still another embodiment of the present invention, the content is 1% to 35% by mass. In still another embodiment of the present invention, the content is 1% to 32% by mass. In still another embodiment of the present invention, the content is 1% to 30% by mass. In still another embodiment of the present invention, the content is 1% to 28% by mass. In still another embodiment of the present invention, the content is 1% to 27% by mass.
- the content is 1% to 26% by mass. In still another embodiment of the present invention, the content is 1% to 24% by mass. In still another embodiment of the present invention, the content is 1% to 21% by mass. In still another embodiment of the present invention, the content is 1% to 20% by mass. In still another embodiment of the present invention, the content is 1% to 19% by mass. In still another embodiment of the present invention, the content is 1% to 16% by mass. In still another embodiment of the present invention, the content is 1% to 15% by mass. In still another embodiment of the present invention, the content is 11% to 49% by mass. In still another embodiment of the present invention, the content is 12% to 49% by mass.
- the content is 13% to 49% by mass. In still another embodiment of the present invention, the content is 15% to 49% by mass. In still another embodiment of the present invention, the content is 16% to 49% by mass. In still another embodiment of the present invention, the content is 17% to 49% by mass. In still another embodiment of the present invention, the content is 20% to 49% by mass. In still another embodiment of the present invention, the content is 23% to 49% by mass. In still another embodiment of the present invention, the content is 24% to 49% by mass. In still another embodiment of the present invention, the content is 25% to 49% by mass. In still another embodiment of the present invention, the content is 28% to 49% by mass.
- the content is 30% to 49% by mass. In still another embodiment of the present invention, the content is 33% to 49% by mass. In still another embodiment of the present invention, the content is 35% to 49% by mass. In still another embodiment of the present invention, the content is 38% to 49% by mass. In still another embodiment of the present invention, the content is 39% to 49% by mass. In still another embodiment of the present invention, the content is 45% to 49% by mass. In still another embodiment of the present invention, the content is 11% to 44% by mass. In still another embodiment of the present invention, the content is 12% to 24% by mass. In still another embodiment of the present invention, the content is 13% to 16% by mass.
- the content is 15% to 32% by mass. In still another embodiment of the present invention, the content is 15% to 21% by mass. In still another embodiment of the present invention, the content is 17% to 20% by mass. In still another embodiment of the present invention, the content is 16% to 27% by mass. In still another embodiment of the present invention, the content is 17% to 28% by mass. In still another embodiment of the present invention, the content is 20% to 35% by mass. In still another embodiment of the present invention, the content is 23% to 26% by mass. In still another embodiment of the present invention, the content is 24% to 40% by mass. In still another embodiment of the present invention, the content is 28% to 38% by mass.
- the content is 30% to 38% by mass. In still another embodiment of the present invention, the content is 25% to 36% by mass. In still another embodiment of the present invention, the content is 27% to 30% by mass. In still another embodiment of the present invention, the content is 30% to 40% by mass. In still another embodiment of the present invention, the content is 30% to 39% by mass. In still another embodiment of the present invention, the content is 35% to 44% by mass. In still another embodiment of the present invention, the content is 35% to 40% by mass. In still another embodiment of the present invention, the content is 33% to 47% by mass. In still another embodiment of the present invention, the content is 39% to 47% by mass. In still another embodiment of the present invention, the content is 38% to 45% by mass.
- the compound represented by the general formula (I-1-2) is preferably a compound selected from the group of compounds represented by the formulas (2.1) to (2.8). .2) to the compound represented by formula (2.4).
- the compound represented by the formula (2.2) is preferable because the response speed of the liquid crystal composition of the present invention is particularly improved.
- the content of the compounds represented by formula (2.3) and formula (2.4) is preferably less than 30% in order to improve solubility at low temperatures.
- the content of the compound represented by the formula (2.2) is preferably 1% by mass or more and 70% by mass or less with respect to the total mass of the liquid crystal composition of the present invention. It is preferably 1% by mass or more and 65% by mass or less, preferably 1% by mass or more and 60% by mass or less, more preferably 1% by mass or more and 55% by mass or less, and preferably 1% by mass or more and 50% by mass or less.
- the content is preferably 5% by mass or more and 50% by mass or less.
- the content of the compound represented by the formula (2.3) is preferably 1% by mass or more and 30% by mass or less based on the total mass of the liquid crystal composition of the present invention. It is preferably 1% by mass or more and 25% by mass or less, preferably 3% by mass or more and 25% by mass or less, preferably 4% by mass or more and 22% by mass or less, and more preferably 5% by mass or more and 22% by mass or less. It is preferably 11% by mass or more and 22% by mass or less, more preferably 13% by mass or more and 22% by mass or less, and preferably 4% by mass or more and 16% by mass or less. % To 15% by mass, preferably 4% to 10% by mass, preferably 5% to 10% by mass, and 12% to 15% by mass. Rukoto is preferred, it is preferably at most 13 mass% or more 16 wt%.
- the content of the compound represented by the formula (2.4) is preferably 1% by mass or more and 30% by mass or less with respect to the total mass of the liquid crystal composition of the present invention. More preferably, they are 1 mass% or more and 25 mass% or less, It is preferable that they are 3 mass% or more and 25 mass% or less, It is preferable that they are 4 mass% or more and 25 mass% or less, 12 mass% or more and 25 mass% or less. Is preferably 17% by mass or more and 25% by mass or less, more preferably 20% by mass or more and 25% by mass or less, and preferably 4% by mass or more and 20% by mass or less.
- the mass is preferably from 13% by mass to 13% by mass, preferably from 12% by mass to 24% by mass, and more preferably from 17% by mass to 20% by mass.
- the liquid crystal composition of the present invention may further contain a compound represented by the formula (2.5) having a structure similar to that of the compound represented by the general formula (I-1-2).
- the content of the compound represented by the formula (2.5) is preferably contained in an amount of from 0 to 40% by mass, preferably from 1 to 35% by mass, preferably from 1 to 30% by mass, based on the total mass of the liquid crystal composition of the present invention.
- it is contained in an amount of 10 to 30% by mass, preferably 15 to 30% by mass, preferably 20 to 30% by mass, and preferably 25 to 30% by mass. preferable.
- the compound represented by the general formula (I) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (I-2).
- R 13 and R 14 each independently represents an alkyl group having 1 to 5 carbon atoms.
- R 13 and R 14 each independently represents an alkyl group having 1 to 5 carbon atoms.
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types.
- the content of the compound represented by the general formula (I-2) is such that solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, drop mark Therefore, it is necessary to adjust appropriately according to required performance such as image sticking and dielectric anisotropy.
- the content of the compound represented by the general formula (I-2) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 1 to 30% by mass in one embodiment of the present invention.
- the content is 2% to 30% by mass.
- the content is 4% to 30% by mass.
- the content is 4% to 25% by mass.
- the content is 4% to 23% by mass.
- the compound represented by the general formula (I-2) is preferably a compound selected from the group of compounds represented by the formulas (3.1) to (3.4). ), A compound represented by formula (3.3) or formula (3.4).
- the compound represented by the formula (3.2) is preferable because the response speed of the liquid crystal composition of the present invention is particularly improved.
- the content of the compounds represented by formula (3.3) and formula (3.4) is preferably less than 20% in order to improve the solubility at low temperatures.
- the compound represented by the general formula (I-2) is preferably a compound selected from the group of compounds represented by the formulas (3.1) to (3.4). ), A compound represented by formula (3.3) and / or formula (3.4).
- the content of the compound represented by the formula (3.3) is 1% by mass or more and 25% by mass or less with respect to the total mass of the liquid crystal composition of the present invention. It is preferably 1% by mass or more and 20% by mass or less, preferably 1% by mass or more and 15% by mass or less, and more preferably 1% by mass or more and 10% by mass or less, and preferably 1% by mass or more and 5% by mass or less. The following is preferable.
- the compound represented by the general formula (I) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (I-3).
- R 13 represents the same meaning as in general formula (I-2).
- the content of the compound represented by the general formula (I-3) includes solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, dropping trace Therefore, it is necessary to adjust appropriately according to required performance such as image sticking and dielectric anisotropy.
- the preferable range of the content is as shown in the following table.
- the content of the compound represented by the general formula (I-3) is, for example, 3 to 30% by mass in one embodiment of the present invention.
- the content is 4% to 30% by mass.
- the content is 15% to 30% by mass.
- the content is 25% to 30% by mass.
- the content is 3% to 25% by mass.
- the content is 3% to 20% by mass.
- the content is 3% to 15% by mass.
- the content is 3% to 5% by mass.
- the compound represented by the general formula (I-3) is preferably a compound selected from the group of compounds represented by the formulas (4.1) to (4.3). It is preferable that it is a compound represented by this.
- the content of the compound represented by the formula (4.3) is preferably 2% by mass or more and 30% by mass or less, and preferably 4% by mass or more and 30% by mass with respect to the total mass of the liquid crystal composition of the present invention.
- % Or less preferably 6% by mass or more and 30% by mass or less, preferably 8% by mass or more and 30% by mass or less, and preferably 10% by mass or more and 30% by mass or less, It is preferably 12% by mass to 30% by mass, preferably 14% by mass to 30% by mass, more preferably 16% by mass to 30% by mass, and 18% by mass to 25% by mass. It is preferable that it is 20 mass% or more and 24 mass% or less, and it is especially preferable that it is 22 mass% or more and 23 mass% or less.
- the compound represented by the general formula (I) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (I-0).
- R 1b represents the same meaning as R 1 in the general formula (L)
- R 2b represents the same meaning as R 2 in the general formula (L)
- n 1b represents 1
- a 1b represents the same meaning as A 1 in the general formula (L)
- Z 1b represents the same meaning as Z 1 in the general formula (L).
- one type is selected.
- the content of the compound represented by the general formula (I-0) is from 1% by mass to 55% by mass with respect to the total mass of the liquid crystal composition of the present invention. It is preferably 1% by mass or more and 50% by mass or less, and preferably 5% by mass or more and 50% by mass or less.
- the content of the compound represented by the formula (2.3) is preferably 1% by mass or more and 30% by mass or less based on the total mass of the liquid crystal composition of the present invention. It is preferably 1% by mass or more and 25% by mass or less, preferably 3% by mass or more and 25% by mass or less, preferably 4% by mass or more and 22% by mass or less, and more preferably 5% by mass or more and 22% by mass or less. It is preferably 11% by mass or more and 22% by mass or less, more preferably 13% by mass or more and 22% by mass or less, and preferably 4% by mass or more and 16% by mass or less. % To 15% by mass, preferably 4% to 10% by mass, preferably 5% to 10% by mass, and 12% to 15% by mass. Preferably there is preferably no greater than 13 wt% or more 16 wt%.
- the content of the compound represented by the general formula (I-0) is low temperature solubility, transition temperature, electrical reliability, birefringence, process compatibility, viscosity, It is necessary to adjust appropriately according to required performance such as dripping marks, image sticking, and dielectric anisotropy.
- a compound represented by the general formula (II-2) described later is contained in the composition from the viewpoint of increasing the response speed of the liquid crystal composition.
- the compound represented by the general formula (I) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (I-4).
- R 11 and R 12 have the same meaning as in general formula (L).
- R 11 and R 12 have the same meaning as in general formula (L).
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types.
- the content of the compound represented by the general formula (I-4) is such that solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, dropping trace Therefore, it is necessary to adjust appropriately according to required performance such as image sticking and dielectric anisotropy.
- the formula (5.4) described later is preferably contained in the composition from the viewpoint of increasing the response speed of the liquid crystal composition. Further, it preferred in view of the even-odd effect and elastic constant (K 33).
- the content of the compound represented by the general formula (I-4) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 2 to 30% by mass in one embodiment of the present invention.
- the content is 5% to 30% by mass.
- the content is 6% to 30% by mass.
- the content is 8% to 30% by mass.
- the content is 10% to 30% by mass.
- the content is 12% to 30% by mass.
- the content is 15% to 30% by mass.
- the content is 20% to 30% by mass.
- the content is 25% to 30% by mass. In still another embodiment of the present invention, the content is 2% to 25% by mass. In still another embodiment of the present invention, the content is 2% to 20% by mass. In still another embodiment of the present invention, the content is 2% to 15% by mass. In still another embodiment of the present invention, the content is 2% to 10% by mass. In still another embodiment of the present invention, the content is 5% to 8% by mass.
- the type of compound that can be combined with the compound represented by the general formula (I-4) is not particularly limited, but solubility at low temperature, transition temperature, electrical reliability are not limited. Combined according to required performance such as properties and birefringence.
- the number of compounds used is, for example, 1 to 10 in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are 1 to 8 types. In another embodiment of the present invention, there are 1 to 5 types. In another embodiment, there are 1-3.
- the effect is high when the content is set to be large.
- the effect is high when the content is set low.
- the compound represented by the general formula (I-4) is preferably a compound selected from the group of compounds represented by the formulas (5.1) to (5.4). To a compound represented by formula (5.7), more preferably at least one compound selected from the group consisting of formulas (5.2) to (5.4). .
- one of the substituents at the end of the skeleton represented by the general formula (I-4) contains an alkenyl group having 1 to 8 carbon atoms, it is preferable from the viewpoint of high-speed response of the liquid crystal composition.
- the content of the compounds represented by the formulas (5.1) to (5.7) is preferably 1% by mass or more and 30% by mass or less with respect to the total mass of the liquid crystal composition of the present invention. .
- the compound represented by the general formula (I) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (I-5).
- R 11 and R 12 have the same meaning as in general formula (I).
- limiting in particular in the kind of compound which can be combined It combines according to performance requested
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types.
- the content of the compound represented by the general formula (I-5) is low temperature solubility, transition temperature, electrical reliability, birefringence index, process suitability, dripping trace. Therefore, it is necessary to adjust appropriately according to required performance such as image sticking and dielectric anisotropy.
- the preferable range of the content is as shown in the following table.
- the content of the compound represented by the general formula (I-5) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 1 to 30% by mass in one embodiment of the present invention.
- the content is 1% to 25% by mass.
- the content is 1% to 20% by mass.
- the content is 1% to 15% by mass.
- the content is 1% to 11% by mass.
- the content is 1% to 8% by mass.
- the content is 1% to 5% by mass.
- the content is 1% to 4% by mass.
- the content is 4% to 11% by mass. In still another embodiment of the present invention, the content is 5% to 11% by mass. In still another embodiment of the present invention, the content is 8% to 11% by mass. In still another embodiment of the present invention, the content is 10% to 11% by mass.
- the compound represented by the general formula (I-5) is preferably a compound selected from the group of compounds represented by the formulas (6.1) to (6.6). ), A compound represented by formula (6.4) and formula (6.6).
- the content of the compounds represented by the above formulas (6.1) to (6.6) is, for example, 1 to 30% by mass in one embodiment of the present invention.
- the content is 1% to 25% by mass.
- the content is 1% to 20% by mass.
- the content is 1% to 15% by mass.
- the content is 1% to 11% by mass.
- the content is 1% to 8% by mass.
- the content is 1% to 5% by mass.
- the content is 1% to 4% by mass.
- the content is 4% to 11% by mass. In still another embodiment of the present invention, the content is 5% to 11% by mass. In still another embodiment of the present invention, the content is 6% to 11% by mass. In still another embodiment of the present invention, the content is 8% to 11% by mass.
- the liquid crystal composition of the present invention further contains compounds represented by formulas (6.7) to (6.11) having a structure similar to that of the compound represented by formula (I-5). You can also.
- the content of the compounds represented by the above formulas (6.7) to (6.10) is, for example, 1 to 15% by mass in one embodiment of the present invention.
- the content is 1% to 14% by mass.
- the content is 1% to 12% by mass.
- the content is 1% to 11% by mass.
- the content is 1% to 10% by mass.
- the content is 1% to 9% by mass.
- the content is 1% to 5% by mass.
- the content is 1% to 4% by mass.
- the content is 3% to 11% by mass. In still another embodiment of the present invention, the content is 4% to 11% by mass. In still another embodiment of the present invention, the content is 5% to 11% by mass. In still another embodiment of the present invention, the content is 6% to 11% by mass.
- the compound represented by the general formula (A) according to the present invention is preferably a compound selected from the compound group represented by the general formula (I-6).
- the content of the compound represented by the general formula (I-6) is preferably 2% by mass or more and 30% by mass or less with respect to the total mass of the liquid crystal composition of the present invention, and is 4% by mass or more and 30% by mass. % Or less, preferably 5% by mass or more and 30% by mass or less, preferably 6% by mass or more and 30% by mass or less, and preferably 9% by mass or more and 30% by mass or less, It is preferably 12% by mass to 30% by mass, preferably 14% by mass to 30% by mass, more preferably 16% by mass to 30% by mass, and 18% by mass to 25% by mass.
- the compound represented by the general formula (I-6) is preferably a compound represented by the formula (7.1).
- the compound represented by the general formula (I) is preferably a compound selected from the group of compounds represented by the general formula (I-7).
- the content of the compound represented by the general formula (I-7) with respect to the total mass of the liquid crystal composition of the present invention is preferably 1% by mass to 20% by mass, and preferably 1% by mass to 15% by mass. It is preferable that it is 1 mass% or more and 10 mass% or less, and it is preferable that it is 1 mass% or more and 5 mass% or less.
- the compound represented by the general formula (I-7) is preferably a compound represented by the formula (8.1).
- the compound represented by the general formula (I) is preferably a compound selected from the group of compounds represented by the general formula (I-8).
- R 16 and R 17 each independently represents an alkenyl group having 2 to 5 carbon atoms
- R 16 and R 17 each independently represents an alkenyl group having 2 to 5 carbon atoms
- required such as solubility at low temperature, transition temperature, electrical reliability, birefringence
- the content of the compound represented by the general formula (I-8) is the solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, drop mark, image sticking, dielectric constant.
- the liquid crystal composition of the present invention is preferably 1 to 30% by mass, preferably 1 to 25% by mass, and preferably 1 to 20% by mass with respect to the total mass of the liquid crystal composition of the present invention.
- % Preferably 1 to 18% by mass, preferably 3 to 18% by mass, preferably 4 to 9% by mass, and preferably 4 to 6% by mass. .
- the compound represented by the general formula (I-8) is preferably a compound selected from the group of compounds represented by the formulas (9.1) to (9.10). ), A compound represented by formula (9.4) and formula (9.7) is preferable.
- the compound represented by the general formula (L) according to the present invention is preferably a compound selected from, for example, compounds represented by the general formula (II).
- R 21 and R 22 each independently represents an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms. It represents, a 2 represents a 1,4-cyclohexylene group or 1,4-phenylene group, Q 2 is a single bond, -COO -, - CH 2 -CH 2 - or an -CF 2 O-).
- limiting in particular in the kind of compound which can be combined It combines according to performance requested
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Moreover, in another embodiment of this invention, they are three types. Furthermore, in another embodiment of this invention, they are four or more types.
- the content of the compound represented by the general formula (II) includes solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, dripping marks, and burn-in. Therefore, it is necessary to appropriately adjust according to required performance such as dielectric anisotropy.
- the content of the compound represented by the general formula (II) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 3 to 35% by mass in one embodiment of the present invention.
- the content is 3% to 30% by mass.
- the content is 3% to 25% by mass.
- the content is 3% to 21% by mass.
- the content is 3% to 20% by mass.
- the content is 3% to 18% by mass.
- the content is 3% to 15% by mass.
- the content is 3% to 12% by mass.
- the content is 4% to 21% by mass. In still another embodiment of the present invention, the content is 11% to 21% by mass. In still another embodiment of the present invention, the content is 13% to 21% by mass. In still another embodiment of the present invention, the content is 15% to 21% by mass. In still another embodiment of the present invention, the content is 16% to 21% by mass. In still another embodiment of the present invention, the content is 4% to 12% by mass. In still another embodiment of the present invention, the content is 11% to 20% by mass. In still another embodiment of the present invention, the content is 13% to 15% by mass. In still another embodiment of the present invention, the content is 15% to 18% by mass.
- the compound represented by the general formula (II) is preferably a compound selected from the group of compounds represented by the general formula (II-1), for example.
- R 21 and R 22 have the same meaning as in general formula (II).
- the content of the compound represented by the general formula (II-1) is preferably adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, and birefringence.
- the preferable range of the content is as shown in the following table.
- the content of the compound represented by the general formula (II-1) is preferably adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, birefringence, 4 mass% or more and 24 mass% or less are preferable, it is preferable that they are 8 mass% or more and 18 mass% or less, and it is still more preferable that they are 12 mass% or more and 14 mass% or less.
- the compound represented by the general formula (II-1) is preferably, for example, a compound represented by the formula (10.1) or the formula (10.2).
- the compound represented by the general formula (II) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (II-2), for example.
- R 23 represents an alkenyl group having 2 to 5 carbon atoms
- R 24 represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms. .
- the compound represented by the general formula (II) is preferably a compound selected from the compound group represented by the general formula (II-3), for example.
- R 25 represents an alkyl group having 1 to 5 carbon atoms
- R 24 represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms. .
- the content of the compound represented by the general formula (II-3) is solubility at low temperature, transition temperature, electrical reliability, birefringence, process compatibility, dripping marks, image sticking, dielectric anisotropy It is necessary to adjust appropriately according to the required performance.
- the preferable content of the compound represented by the general formula (II-3) is, for example, 2 to 45% by mass with respect to the total mass of the liquid crystal composition of the present invention.
- the mass% is preferably 2 to 10 mass%.
- the compound represented by the general formula (II-3) is preferably a compound represented by, for example, the formula (12.1) to the formula (12.3).
- the formula (12.2) Or a compound represented by formula (12.1) and a compound represented by formula (12.2) may be an optically active compound.
- the preferable content of the compounds represented by the formulas (12.1) to (12.3) is, for example, 1 to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention.
- 1 to 13% by mass, 1 to 10% by mass, 2 to 15% by mass, 2 to 14% by mass, 2 to 11% by mass, and 3 to 10% by mass are preferable.
- the compound represented by the general formula (II-3) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (II-3-1), for example.
- R 25 represents an alkyl group having 1 to 5 carbon atoms
- R 26 represents an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (II-3-1) can be adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, and birefringence. It is preferably 1% by mass or more and 24% by mass or less, preferably 4% by mass or more and 18% by mass or less, and more preferably 6% by mass or more and 14% by mass or less.
- the compound represented by the general formula (II-3-1) is preferably, for example, a compound represented by the formula (13.1) to the formula (13.4), in particular, the formula (13.3). It is preferable that it is a compound represented by this.
- the compound represented by the general formula (II) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (II-4), for example.
- R 21 and R 22 are each independently an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms. Represents.) Of these compounds, only one kind or two or more kinds may be contained, but it is preferable to combine them appropriately according to the required performance. There are no particular restrictions on the types of compounds that can be combined, but depending on the required performance such as solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc., 1 to 2 of these compounds It is preferable to include types, and it is more preferable to include one to three types.
- the content of the compound represented by the general formula (II-4) is preferably 1% by mass or more and 15% by mass or less, and preferably 2% by mass or more and 15% by mass with respect to the total mass of the liquid crystal composition of the present invention. % Or less, preferably 3% by mass or more and 15% by mass or less, preferably 4% by mass or more and 12% by mass or less, and more preferably 5% by mass or more and 7% by mass or less.
- the compound represented by the general formula (II-4) is preferably, for example, a compound represented by the formula (14.1) to the formula (14.5), and in particular, the formula (14.2) or / And a compound represented by the formula (14.5) is preferable.
- the compound represented by the general formula (II) according to the present invention is preferably a compound selected from, for example, a compound group represented by the general formula (II-5).
- R 25 represents an alkyl group or an alkoxy group of 1 to 4 carbon atoms alkenyl or carbon atom number of 1 to 5 carbon atoms 2 ⁇
- Y 26 Represents a hydrogen atom, a fluorine atom, CF 3 , OCF 3 , an alkenyl group having 2 to 8 carbon atoms, an alkyl group having 1 to 8 carbon atoms or an alkoxy group having 1 to 8 carbon atoms
- X 21 and X 22 each independently represents a hydrogen atom or a fluorine atom.
- These compounds may contain only one kind or two or more kinds, but it is preferable to combine them appropriately according to the required performance.
- the content of the compound represented by the general formula (II-5) is preferably 1% by mass or more and 30% by mass or less, and preferably 2% by mass or more and 28% by mass with respect to the total mass of the liquid crystal composition of the present invention. % Or less, preferably 3% by mass or more and 27% by mass or less, preferably 4% by mass or more and 26% by mass or less, and more preferably 5% by mass or more and 25% by mass or less.
- the compound represented by the general formula (L) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (III).
- R 31 and R 32 each independently represents an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (III) is 1% by mass or more and 25% by mass or less based on the total mass of the liquid crystal composition of the present invention in consideration of required solubility and birefringence. It is preferable to contain 2 to 20% by weight, preferably 2 to 15% by weight, preferably 2 to 10% by weight, preferably 4% by weight. % To 6% by mass is preferable.
- the compound represented by the general formula (III) is preferably, for example, a compound represented by the formula (15.1) or the formula (15.2), and particularly represented by the formula (15.1). It is preferable that it is a compound.
- the compound represented by the general formula (III) is preferably a compound selected from the group of compounds represented by the general formula (III-1).
- R 33 represents an alkenyl group having 2 to 5 carbon atoms.
- R 32 each independently represents an alkyl group having 1 to 5 carbon atoms or an alkyl group having 1 to 4 carbon atoms. Represents an alkoxy group.
- the content of the compound represented by the general formula (III-1) is preferably adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, and birefringence. . 4 mass% or more and 23 mass% or less are preferable with respect to the total mass of the liquid-crystal composition of this invention, 6 mass% or more and 18 mass% or less are preferable, and it is 10 mass% or more and 13 mass% or less. preferable.
- the compound represented by the general formula (III-1) is preferably, for example, a compound represented by the formula (16.1) to the formula (16.10).
- the compound represented by the general formula (III) is preferably a compound selected from the group of compounds represented by the general formula (III-2).
- R 31 has the same meaning as in general formula (III).
- the content of the compound represented by the general formula (III-2) is preferably adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, birefringence, 4 mass% or more and 23 mass% or less are preferable with respect to the total mass of the liquid-crystal composition of this invention, 6 mass% or more and 18 mass% or less are preferable, and it is 10 mass% or more and 13 mass% or less. preferable.
- the compound represented by the general formula (III-2) is preferably a compound selected from the group of compounds represented by formula (17.1) to formula (17.3), for example, It is preferable that it is a compound represented by 17.3).
- the compound represented by the general formula (L) according to the present invention is preferably selected from the group represented by the general formula (IV).
- R 41 and R 42 each independently represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms
- X 41 and X 42 each independently represent Represents a hydrogen atom or a fluorine atom.
- a compound having a structure of the general formula (IV) such as a compound represented by the following formulas (18.1) to (18.9) is added to the liquid crystal composition, ⁇ n of the liquid crystal composition or other liquid crystal
- the solubility with the component which comprises a composition improves.
- the number of compounds used is, for example, 1 to 6 in one embodiment of the present invention.
- the content of the compound represented by the general formula (IV) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 1 to 35% by mass in one embodiment. In still another embodiment of the present invention, the content is 1% to 30% by mass. In still another embodiment of the present invention, the content is 1% to 26% by mass. In still another embodiment of the present invention, the content is 1% to 22% by mass. In still another embodiment of the present invention, the content is 1% to 10% by mass. In still another embodiment of the present invention, the content is 1% to 8% by mass. In still another embodiment of the present invention, the content is 1% to 6% by mass. In still another embodiment of the present invention, the content is 2% to 26% by mass.
- the content is 3% to 26% by mass. In still another embodiment of the present invention, the content is 11% to 26% by mass. In still another embodiment of the present invention, the content is 20% to 26% by mass. In still another embodiment of the present invention, the content is 2% to 8% by mass. In still another embodiment of the present invention, the content is 2% to 6% by mass. In still another embodiment of the present invention, the content is 11% to 22% by mass.
- the compound represented by the general formula (IV) is preferably a compound selected from the group of compounds represented by the general formula (IV-1), for example.
- R 43 and R 44 each independently represents an alkyl group having 1 to 5 carbon atoms.
- the content of the compound represented by the general formula (IV-1) is solubility at low temperature, transition temperature, electrical reliability, birefringence, process compatibility, dripping marks, image sticking, dielectric anisotropy It is necessary to adjust appropriately according to the required performance.
- the content of the compound represented by the general formula (IV-1) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 1 to 35% by mass in one embodiment. In still another embodiment of the present invention, the content is 1% to 30% by mass. In still another embodiment of the present invention, the content is 1% to 26% by mass. In still another embodiment of the present invention, the content is 1% to 22% by mass. In still another embodiment of the present invention, the content is 1% to 10% by mass. In still another embodiment of the present invention, the content is 1% to 8% by mass. In still another embodiment of the present invention, the content is 1% to 6% by mass. In still another embodiment of the present invention, the content is 2% to 26% by mass.
- the content is 3% to 26% by mass. In still another embodiment of the present invention, the content is 11% to 26% by mass. In still another embodiment of the present invention, the content is 20% to 26% by mass. In still another embodiment of the present invention, the content is 2% to 8% by mass. In still another embodiment of the present invention, the content is 2% to 6% by mass. In still another embodiment of the present invention, the content is 11% to 22% by mass.
- the compound represented by the general formula (IV-1) is preferably a compound represented by, for example, the formula (18.1) to the formula (18.9).
- the compound represented by the general formula (IV-1) there are no particular limitations on the types of compounds that can be combined. However, it is preferable to contain 1 to 3 of these compounds, and 1 to 4 It is more preferable to contain the types.
- a wide molecular weight distribution of a compound selected from the group of compounds represented by the general formula (IV-1) is also effective for solubility.
- 1 type from the compound represented 1 type from the compound represented by Formula (18.4) or (18.5), 1 type from the compound represented by Formula (18.6) or Formula (18.7)
- the compound represented by Formula (18.1), Formula (18.3), Formula (18.4), Formula (18.6) and Formula (18.9) is included.
- the compound represented by the general formula (L) according to the present invention is preferably a compound selected from the group represented by the general formula (V).
- R 51 and R 52 each independently represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- a 51 and A 52 each independently represents a 1,4-cyclohexylene group or a 1,4-phenylene group, Q 5 represents a single bond or —COO—, and
- X 51 and X 52 each independently represent Represents a fluorine atom or a hydrogen atom.
- the kind of compound to be used is, for example, one kind in one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of this invention, they are four types.
- the content of the compound represented by the general formula (V) with respect to the total mass of the liquid crystal composition according to the present invention is, for example, 1 to 25% by mass in one embodiment. In still another embodiment of the present invention, the content is 1% to 20% by mass. In still another embodiment of the present invention, the content is 1% to 19% by mass. In still another embodiment of the present invention, the content is 1% to 10% by mass. In still another embodiment of the present invention, the content is 1% to 9% by mass. In still another embodiment of the present invention, the content is 1% to 8% by mass. In still another embodiment of the present invention, the content is 1% to 7% by mass. In still another embodiment of the present invention, the content is 1% to 5% by mass.
- the content is 1% to 3% by mass. In still another embodiment of the present invention, the content is 1% to 2% by mass. In still another embodiment of the present invention, the content is 2% to 19% by mass. In still another embodiment of the present invention, the content is 5% to 19% by mass. In still another embodiment of the present invention, the content is 9% to 19% by mass. In still another embodiment of the present invention, the content is 2% to 8% by mass. In still another embodiment of the present invention, the content is 6% to 8% by mass.
- the compound represented by the general formula (V) according to the present invention is preferably a compound represented by the general formula (V-1).
- R 51 and R 52 , X 51 and X 52 represent the same meaning as in the general formula (V)).
- the compound represented by the general formula (V-1) is preferably a compound represented by the general formula (V-1-1).
- R 51 and R 52 represent the same meaning as in the general formula (V).
- the compound represented by the general formula (V-1-1) is preferably contained in an amount of 1% by mass or more and 15% by mass or less based on the total mass of the liquid crystal composition of the present invention. It is further preferable to contain 3 to 10% by weight, preferably 3 to 7% by weight, preferably 3 to 5% by weight, It is preferable to contain 3 mass% or more and 4 mass% or less.
- the compound represented by the general formula (V-1-1) is preferably a compound represented by the formula (20.1) to the formula (20.4). It is preferable that it is a compound represented.
- the compound represented by the general formula (V-1) according to the present invention is preferably a compound represented by the general formula (V-1-2).
- R 51 and R 52 represent the same meaning as in the general formula (V).
- the compound represented by the general formula (V-1-2) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention.
- the content is preferably 1% by mass or more and 7% by mass or less, and more preferably 1% by mass or more and 5% by mass or less.
- the compound represented by the general formula (V-1-2) is preferably a compound represented by the formula (21.1) to the formula (21.3). It is preferable that it is a compound represented.
- the compound represented by the general formula (V-1) according to the present invention is preferably a compound represented by the general formula (V-1-3).
- R 51 and R 52 have the same meaning as in the general formula (V).
- the compound represented by the general formula (V-1-3) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention, and preferably 2% by mass to 15% by mass.
- the content is preferably 3% by mass or more and 10% by mass or less, and more preferably 4% by mass or more and 8% by mass or less.
- the compound represented by the general formula (V-1-3) is a compound represented by the formula (22.1) to the formula (22.3). It is preferable that it is a compound represented by Formula (22.1).
- the compound represented by the general formula (V) according to the present invention is preferably a compound represented by the general formula (V-2).
- R 51 and R 52 , X 51 and X 52 represent the same meaning as in the general formula (V).
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, it is two or more types.
- the content of the compound represented by the general formula (V-2) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 1 to 30% by mass in one embodiment. In still another embodiment of the present invention, the content of the compound is 2% to 25% by mass. In still another embodiment of the present invention, the content of the compound is 5% to 19% by mass. In still another embodiment of the present invention, the content of the compound is 6% to 10% by mass. In still another embodiment of the present invention, the content of the compound is 10% to 19% by mass. In still another embodiment of the present invention, the content of the compound is 4% to 8% by mass.
- the compound represented by the general formula (V-2) according to the present invention is preferably a compound represented by the general formula (V-2-1).
- R 51 and R 52 represent the same meaning as in the general formula (V).
- the compound represented by the general formula (V-2-1) is preferably a compound represented by the formula (23.1) to the formula (23.4), and the formula (23.1) or / And a compound represented by the formula (23.2) is preferable.
- the compound represented by the general formula (V-2) according to the present invention is preferably a compound represented by the general formula (V-2-2).
- R 51 and R 52 represent the same meaning as in the general formula (V).
- the compound represented by the general formula (V-2-2) is preferably a compound represented by the formula (24.1) to the formula (24.4), and the formula (24.1) or / And a compound represented by the formula (24.2) is preferable.
- the compound represented by the general formula (V) according to the present invention is preferably a compound represented by the general formula (V-3).
- R 51 and R 52 have the same meaning as in general formula (V).
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of this invention, they are three or more types.
- the compound represented by the general formula (V-3) is preferably contained in an amount of 1% by mass or more and 16% by mass or less, preferably 1% by mass or more and 13% by mass or less based on the total mass of the liquid crystal composition of the present invention. It is preferable to contain 1 mass% or more and 9 mass% or less, and it is preferable to contain 3 mass% or more and 9 mass% or less.
- the compound represented by the general formula (V-3) is preferably a compound represented by the formula (25.1) to the formula (24.3).
- the compound represented by the general formula (V) according to the present invention is preferably a compound represented by the general formula (V-4).
- R 51 and R 52 each independently represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkyl group having 1 to 4 carbon atoms. Represents an alkoxy group.
- the compound represented by the general formula (V-4) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention, and preferably 2% by mass or more and 15% by mass or less. It is preferable to contain 3 mass% or more and 10 mass% or less, and it is preferable to contain 4 mass% or more and 8 mass% or less.
- the compound represented by the general formula (V-4) is preferably at least one compound selected from the group of compounds represented by formula (25.11) to formula (25.13), It is more preferable that it is a compound represented by Formula (25.13).
- the compound represented by the general formula (L) according to the present invention is preferably a compound represented by the general formula (V′-5).
- R 51 and R 52 each independently represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or 1 to 4 carbon atoms.
- the compound represented by the general formula (V′-5) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention, and preferably 2% by mass to 15% by mass. It is preferable to contain, it is preferable to contain 2 to 10 mass%, and it is preferable to contain 5 to 10 mass%.
- the compound represented by the general formula (V′-5) is preferably at least one compound selected from the group of compounds represented by formulas (25.21) to (25.24). More preferably, it is a compound represented by formula (25.21) and / or formula (25.23).
- the liquid crystal composition of the present invention preferably further contains at least one selected from the group consisting of a compound represented by the general formula (VI) and a compound represented by the general formula (VII).
- the compound represented by the general formula (L) according to the present invention is preferably a compound represented by the general formula (VI) and / or a compound represented by the general formula (VII).
- R 61 R 62 , R 71 and R 72 are each independently a linear alkyl group having 1 to 10 carbon atoms and a linear alkoxy group having 1 to 10 carbon atoms. Represents a group or a straight-chain alkenyl group having 2 to 10 carbon atoms.)
- the compound represented by the general formula (VI) specifically, the following compounds can be preferably used.
- each of the compounds represented by the general formula (VI) or the general formula (VII) there is no particular limitation on the types of compounds that can satisfy the respective structural formulas, but the solubility at low temperatures, the transition temperature, In accordance with required performance such as electrical reliability and birefringence, it is preferable to mix 1 to 3 types of compounds satisfying the respective formulas, more preferably 1 to 4 types, It is particularly preferable to contain 1 to 5 or more types.
- the content of the compound represented by the general formula (VI) is preferably 0 to 35% by mass, and preferably 0 to 25% by mass with respect to the total mass of the liquid crystal composition of the present invention. 0 to 15% by mass is preferable.
- the content of the compound represented by the general formula (VII) is preferably 0 to 35% by mass, more preferably 0 to 25% by mass, and more preferably 0 to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention. % Is preferred.
- the liquid crystal composition according to the present invention may further contain a compound represented by the following general formula (M), and the compound represented by the general formula (M) is a polar compound (with a dielectric anisotropy of +5 to +30) is preferred.
- M a compound represented by the following general formula (M)
- M is a polar compound (with a dielectric anisotropy of +5 to +30) is preferred.
- R M1 represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms.
- C M1 and C M2 are each independently (D) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or nonadjacent two or more -CH 2 - may be replaced by -O- or -S- And (e) a 1,4-phenylene group (one —CH ⁇ present in the group or two or more non-adjacent —CH ⁇ may be replaced by —N ⁇ ).
- K M1 and K M2 are each independently a single bond, —CH 2 CH 2 —, — (CH 2 ) 4 —, —OCH 2 —, —CH 2 O—, —OCF 2 —, —CF 2 O—, Represents —COO—, —OCO— or —C ⁇ C—,
- X M1 and X M3 each independently represent a hydrogen atom, a chlorine atom or a fluorine atom
- X M2 represents a hydrogen atom, a fluorine atom, a chlorine atom, a
- the type of compound represented by the general formula (M) that can be combined as the second component but solubility at low temperatures, transition temperature, electrical reliability, dielectric constant, birefringence, etc. Are used in combination according to the desired performance.
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of this invention, they are three types. Furthermore, in another embodiment of the present invention, there are four types. Furthermore, in another embodiment of this invention, they are five types. Furthermore, in another embodiment of the present invention, there are six types. Furthermore, in another embodiment of this invention, they are seven or more types.
- the content of the compound represented by the general formula (M) is low temperature solubility, transition temperature, electrical reliability, birefringence, process suitability, dripping marks, image sticking. Therefore, it is necessary to appropriately adjust according to required performance such as dielectric anisotropy.
- the content of the compound represented by the general formula (M) is 0.5 to 70% by mass with respect to the total mass of the liquid crystal composition of the present invention.
- the content of the compound is 1% to 65% by mass.
- the content of the compound is 1% to 60% by mass.
- the content of the compound is 1% to 55% by mass.
- the content of the compound is 1% to 54% by mass.
- the content of the compound is 1% to 51% by mass.
- the content of the compound is 1% to 47% by mass.
- the content of the compound is 1% to 42% by mass.
- the content of the compound is 1% to 40% by mass.
- the content of the compound is 1% to 39% by mass.
- the content of the compound is 1% to 37% by mass.
- the content of the compound is 1% to 35% by mass.
- the content of the compound is 1% to 33% by mass.
- the content of the compound is 1% to 32% by mass.
- the content of the compound is 1% to 31% by mass.
- the content of the compound is 1% to 30% by mass.
- the content of the compound is 1% to 29% by mass.
- the content of the compound is 1% to 25% by mass.
- the content of the compound is 1% to 24% by mass.
- the content of the compound is 1% to 20% by mass.
- the content of the compound is 1% to 19% by mass.
- the content of the compound is 1% to 10% by mass.
- the content of the compound is 1% to 9% by mass.
- the content of the compound is 1% to 8% by mass.
- the content of the compound is 3% to 54% by mass.
- the content of the compound is 9% to 54% by mass.
- the content of the compound is 19% to 54% by mass.
- the content of the compound is 20% to 54% by mass.
- the content of the compound is 22% to 54% by mass.
- the content of the compound is 26 to 54% by mass.
- the content of the compound is 28% to 54% by mass.
- the content of the compound is 29% to 54% by mass.
- the content of the compound is 30% to 54% by mass.
- the content of the compound is 31% to 54% by mass.
- the content of the compound is 32% to 54% by mass.
- the content of the compound is 33% to 54% by mass.
- the content of the compound is 39% to 54% by mass.
- the content of the compound is 42% to 54% by mass.
- the content of the compound is 46% to 54% by mass.
- the content of the compound is 48% to 54% by mass.
- the content of the compound is 52% to 54% by mass.
- the content of the compound is 3% to 8% by mass.
- the content of the compound is 9% to 10% by mass.
- the content of the compound is 19% to 25% by mass.
- the content of the compound is 22% to 24% by mass.
- the content of the compound is 26 to 29% by mass.
- the content of the compound is 28% to 35% by mass.
- the content of the compound is 28% to 33% by mass.
- the content of the compound is 31% to 32% by mass.
- the content of the compound is 32% to 33% by mass.
- the content of the compound is 33% to 42% by mass.
- the content of the compound is 39% to 42% by mass.
- the content of the compound is 42% to 47% by mass.
- the content of the compound is 48% to 51% by mass.
- the liquid crystal composition of the present invention maintains a low viscosity and a liquid crystal composition having a high response speed is required, it is preferable to lower the lower limit value and lower the upper limit value. Furthermore, when the liquid crystal composition of the present invention maintains a high Tni and a liquid crystal composition with good temperature stability is required, it is preferable to lower the lower limit and lower the upper limit. Further, when it is desired to increase the dielectric anisotropy in order to keep the driving voltage low, it is preferable to increase the upper limit value while increasing the lower limit value.
- R M1 represents a linear alkyl group having 1 to 5 carbon atoms or a linear alkoxy group having 1 to 4 carbon atoms when the ring structure to which R M1 is bonded is a phenyl group (aromatic). And an alkenyl group having 4 to 5 carbon atoms, and when the ring structure to which it is bonded is a saturated ring structure such as cyclohexane, pyran and dioxane, a linear alkyl group having 1 to 5 carbon atoms, A straight-chain alkoxy group having 1 to 4 carbon atoms and a straight-chain alkenyl group having 2 to 5 carbon atoms are preferred.
- the compound represented by the general formula (M) according to the present invention preferably does not have a chlorine atom in the molecule when chemical stability of the liquid crystal composition is required. Further, the compound having a chlorine atom in the liquid crystal composition is preferably 5% or less, preferably 3% or less, preferably 1% or less, preferably 0.5% or less, It is preferable not to contain substantially. “Substantially not contained” means that only a compound containing a chlorine atom is mixed into the liquid crystal composition without intentionally forming a compound or the like generated as an impurity during the production of the compound.
- R 3 represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms.
- a 2 is each independently 1,4-cyclohexylenecyclohexylene group, 1,4-phenylene group, tetrahydropyran-2,5-diyl group, dioxane-2,5-diyl group or pyrimidine-2,5- Represents a diyl group, and when A 1 represents a 1,4-phenylene group, one or more hydrogen atoms in the 1,4-phenylene group may be substituted with fluorine atoms, Each Z
- m 1 is preferably 2 or 3.
- m 1 is 2, there is a characteristic of a lower driving voltage. Further, when m 1 is 3, there is a characteristic of a higher transition temperature.
- the compound represented by the general formula (M) according to the present invention is preferably a compound represented by the general formula (X).
- X 101 to X 104 each independently represents a fluorine atom or a hydrogen atom
- Y 10 represents a fluorine atom, a chlorine atom, or —OCF 3
- Q 10 represents a single bond or —CF 2 O—
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms
- a 101 and A 102 are each independently 1,4-cyclohexylene group, 1,4-phenylene group or
- the hydrogen atom on the 1,4-phenylene group may be substituted with a fluorine atom.
- the compounds that can be combined in the compound represented by the general formula (X) are not particularly limited, but are appropriately combined in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, and the like. For example, in one embodiment of the present invention, there is one. In another embodiment of the present invention, there are two types. In yet another embodiment, there are three types. In still another embodiment, there are four types. In still another embodiment, there are five or more types.
- the content of the compound represented by the general formula (X) is appropriately adjusted for each embodiment in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
- the content of the compound represented by the general formula (X) is 1 to 35% by mass in one embodiment of the present invention with respect to the total mass of the liquid crystal composition of the present invention, and in another embodiment.
- the content is 1-9% by weight, in yet another embodiment the content is 1-8% by weight, and in yet another embodiment the content is 1-7% by weight, and in yet another embodiment
- the content is 1 to 3% by mass, and in still another embodiment, the content is 3 to 24% by mass, and in still another embodiment, the content is 5 to 24% by mass, and in still another embodiment, the content is 6-24% by weight, in yet another embodiment the content is 8-24% by weight, in yet another embodiment the content is 11-24% by weight, and in yet another embodiment the content is 13%.
- the content is 15-24% by weight. In still another embodiment, the content is 17-24% by weight. In still another embodiment, the content is 3-7. In yet another embodiment, the content is 5-10% by weight, in yet another embodiment the content is 6-9% by weight, and in yet another embodiment the content is 6-8% by weight. In yet another embodiment, the content is 8-11. %, In yet another embodiment the content is 11-19% by weight, in yet another embodiment the content is 11-12% by weight, and in yet another embodiment the content is 13-16% by weight. In still another embodiment, the content is 15 to 19% by mass, and in still another embodiment, the content is 17 to 20% by mass.
- the liquid crystal composition of the present invention maintains a low viscosity and a liquid crystal composition having a high response speed is required, it is preferable to lower the lower limit value and lower the upper limit value. Furthermore, when a liquid crystal composition that does not easily cause burn-in is required, it is preferable to lower the lower limit value and lower the upper limit value. Further, when it is desired to increase the dielectric anisotropy in order to keep the driving voltage low, it is preferable to increase the upper limit value while increasing the lower limit value.
- the compound represented by the general formula (M) according to the present invention is preferably a compound represented by the general formula (X-1).
- X 101 to X 103 and R 10 have the same meaning as in the general formula (X).
- X there is no restriction
- the content of the compound represented by the general formula (X-1) is appropriately adjusted in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
- the content of the compound represented by the general formula (X-1) is 1 to 20% by mass in one embodiment of the present invention relative to the total mass of the liquid crystal composition of the present invention.
- 1-15% by weight in a form 1-10% by weight in yet another embodiment, 1-9% by weight in yet another embodiment, 1-8% by weight in yet another embodiment, and yet another 1-7% by weight in embodiments, 1-6% by weight in yet another embodiment, 1-3% by weight in yet another embodiment, 3-9% by weight in yet another embodiment, and even more
- 3-7% by weight, yet another implementation 5-7 wt% in the state in yet another embodiment from 6-7% by weight.
- the compound represented by the general formula (X-1) according to the present invention is preferably a compound represented by the general formula (X-1-1).
- R 10 has the same meaning as in general formula (X).
- the content of the compound represented by the general formula (X-1-1) is appropriately adjusted in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
- the content of the compound represented by the general formula (X-1-1) is 1 to 25% by mass in one embodiment of the present invention with respect to the total mass of the liquid crystal composition of the present invention. 1 to 20% by weight in a form, 1 to 15% by weight in yet another embodiment, 1 to 10% by weight in yet another embodiment, 3 to 10% by weight in yet another embodiment, and yet another In the embodiment, it is 5 to 10% by mass.
- the compounds represented by the general formula (X-1-1) used in the liquid crystal composition of the present invention are specifically compounds represented by the formulas (36.1) to (36.4). Among them, it is preferable to contain a compound represented by formula (36.1) and / or formula (36.2).
- the compound represented by the general formula (X-1) used in the liquid crystal composition of the present invention is preferably a compound represented by the general formula (X-1-2).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-1-2) is preferably 1% by mass or more, more preferably 2% by mass or more, based on the total amount of the liquid crystal composition of the present invention.
- the mass% or more is more preferable.
- the maximum ratio is preferably 20% by mass or less, more preferably 16% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
- the compound represented by the general formula (X-1-2) is specifically preferably a compound represented by the formula (37.1) to the formula (37.4). It is preferable to contain the compound represented by 37.2).
- the compound represented by the general formula (X-1) according to the present invention is preferably a compound represented by the general formula (X-1-3).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-1-3) is preferably 1% by mass or more, more preferably 2% by mass or more, based on the total amount of the liquid crystal composition of the present invention.
- the mass% or more is more preferable.
- the maximum ratio is preferably 20% by mass or less, more preferably 16% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
- the compounds represented by the general formula (X-1-3) used in the liquid crystal composition of the present invention are specifically the compounds represented by the formulas (38.1) to (38.4).
- the compound represented by the general formula (X) according to the liquid crystal composition of the present invention is preferably a compound represented by the general formula (X-2).
- X 102 to X 103 each independently represents a fluorine atom or a hydrogen atom
- Y 10 represents a fluorine atom, a chlorine atom, or —OCF 3
- R 10 represents the number of carbon atoms.
- the compound represented by the general formula (X-2) according to the present invention is preferably a compound represented by the general formula (X-2-1).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-2-1) is preferably 1% by mass or more, more preferably 2% by mass or more, based on the total amount of the liquid crystal composition of the present invention.
- the mass% or more is more preferable.
- the maximum ratio is preferably 20% by mass or less, more preferably 16% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
- the compounds represented by the general formula (X-2-1) used in the liquid crystal composition of the present invention are specifically compounds represented by the formulas (39.1) to (39.4).
- the compound represented by the general formula (X-2) according to the present invention is preferably a compound represented by the general formula (X-2-2).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-2-2) is preferably 1% by mass or more, more preferably 2% by mass or more, based on the total amount of the liquid crystal composition of the present invention. % Or more is more preferable.
- the maximum ratio is preferably 20% by mass or less, more preferably 16% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
- the compounds represented by the general formula (X-2-2) used in the liquid crystal composition of the present invention are specifically compounds represented by the formulas (40.1) to (40.4). In particular, it is preferable to contain a compound represented by the formula (40.2).
- the compound represented by the general formula (M) according to the present invention is preferably a compound represented by the general formula (IIb).
- R 3b represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkyl group having 2 to 8 carbon atoms.
- the methylene group in the group may be substituted with an oxygen atom unless oxygen atoms are continuously bonded, and may be substituted with a carbonyl group unless a carbonyl group is bonded continuously;
- a 2b independently represents 1,4-cyclohexylenecyclohexylene group, 1,4-phenylene group, tetrahydropyran-2,5-diyl group, dioxane-2,5-diyl group or pyrimidine-2,5- Represents a diyl group, and when A 2b represents a 1,4-phenylene group, one or more hydrogen atoms in the 1,4-phenylene group may be substituted with fluorine
- the content of the compound represented by the general formula (IIb) is an upper limit value and a lower limit value for each embodiment in consideration of properties such as solubility at low temperature, transition temperature, electrical reliability, and birefringence.
- the lower limit of the content of the compound is 0.01% with respect to the total amount of the liquid crystal composition of the present invention, 0.05% in another embodiment, and yet another implementation. 0.1% in form, 0.2% in yet another embodiment, 0.3% in yet another embodiment, 0.4% in yet another embodiment, and in yet another embodiment 0.5%.
- the upper limit of the content of the compound represented by the general formula (IIb) is, for example, 10% in one embodiment of the present invention, 8% in another embodiment, and 2% in another embodiment. In yet another embodiment, it is 1%, in yet another embodiment 0.8%, and in yet another embodiment 0.7%.
- the compound represented by the general formula (X) according to the present invention is preferably a compound represented by the general formula (X-3).
- X 102 to X 103 each independently represents a fluorine atom or a hydrogen atom
- R 10 represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms. Represents a group or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-3) is preferably 0.1% by mass or more, more preferably 0.2% by mass or more, based on the total amount of the liquid crystal composition of the present invention. 0.3 mass% or more is more preferable.
- the maximum ratio is preferably 8% by mass or less, more preferably 5% by mass or less, and even more preferably 2% by mass or less. 1% by mass or less is particularly preferable.
- the compound represented by the general formula (X-3) used in the liquid crystal composition of the present invention is preferably a compound represented by the general formula (X-3-1).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-3-1) is preferably 0.05% by mass or more, more preferably 0.2% by mass or more with respect to the total amount of the liquid crystal composition of the present invention. Preferably, 0.3 mass% or more is more preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably 5% by mass or less, more preferably 3% by mass or less, and even more preferably 2% by mass or less. 1% by mass or less is particularly preferable.
- the compounds represented by the general formula (X-3-1) used in the liquid crystal composition of the present invention are specifically compounds represented by the formulas (41.1) to (41.4).
- the compound represented by the above formulas (41.1) to (41.4) is included in the liquid crystal composition, not only dielectric properties such as ⁇ can be secured, but also compatibility with the nonpolar first component is impaired. Absent.
- the compound represented by the general formula (X-3) used in the liquid crystal composition of the present invention is preferably a compound represented by the general formula (X-3-1).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-3-2) is preferably 0.05% by mass or more, more preferably 0.2% by mass or more with respect to the total amount of the liquid crystal composition of the present invention. Preferably, 0.3 mass% or more is more preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably 5% by mass or less, more preferably 3% by mass or less, and even more preferably 2% by mass or less. 1.5% by mass or less is particularly preferable.
- the compound represented by the general formula (X-3-2) used in the liquid crystal composition of the present invention is specifically a compound represented by the formula (41.5) to the formula (41.8).
- the compound represented by formula (41.5) to formula (41.7) is included in the liquid crystal composition, not only dielectric properties such as ⁇ can be secured, but also compatibility with the nonpolar first component is impaired. Absent.
- the compound represented by the general formula (X) is preferably a compound represented by the general formula (X-4).
- X 102 represents a fluorine atom or a hydrogen atom
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or 1 to 4 represents an alkoxy group.
- the compound represented by the general formula (X-4) according to the present invention is preferably a compound represented by the general formula (X-4-1).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (X-4-1) is preferably 2% by mass or more, more preferably 5% by mass or more, based on the total amount of the liquid crystal composition of the present invention.
- the mass% or more is more preferable.
- the maximum ratio is preferably 20% by mass or less, more preferably 17% by mass or less, and even more preferably 15% by mass or less. 13 mass% or less is particularly preferable.
- the compound represented by the general formula (X-4-1) used in the liquid crystal composition of the present invention is specifically a compound represented by the formula (42.1) to the formula (42.4).
- the compound represented by the general formula (X) according to the present invention is preferably a compound represented by the general formula (X-5).
- X 102 represents a fluorine atom or a hydrogen atom
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or 1 to 4 represents an alkoxy group.
- the compound represented by the general formula (X-5) used in the liquid crystal composition of the present invention is preferably a compound represented by the general formula (X-5-1).
- R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the compounds represented by the general formula (X-5-1) used in the liquid crystal composition of the present invention are specifically compounds represented by the formulas (43.1) to (43.4).
- the content of the compounds represented by the formulas (43.1) to (43.4) is preferably 1% by mass or more, and preferably 2% by mass or more with respect to the total amount of the liquid crystal composition of the present invention. More preferred is 3% by mass or more.
- the maximum ratio is preferably limited to 18% by mass or less, more preferably 15% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
- the compound represented by the general formula (M) according to the present invention is at least one selected from the group consisting of compounds represented by the following general formulas (X-6-1) and (X-6-2) It is preferable that
- the compound that can be combined in the general formula (X-6-1) is not particularly limited, but solubility at low temperature, transition temperature, electrical reliability, birefringence Considering the rate and the like, for example, one embodiment of the present invention has 1 to 5 types. Alternatively, in another embodiment of the present invention, there are 1 to 4 types. In another embodiment of the present invention, there are 1 to 3 types.
- the content of the compound represented by the general formula (X-6-1) has characteristics such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
- the lower limit of the content is 1% with respect to the total amount of the liquid crystal composition of the present invention, 3% in another embodiment, 4% in yet another embodiment, and further 5% in another embodiment, 6% in yet another embodiment, 7% in yet another embodiment, and 8% in yet another embodiment. In still another embodiment, it is 9%.
- the upper limit of the content of the compound represented by the general formula (X-6-1) is, for example, 30% in one embodiment of the present invention, and another embodiment 28%, yet another embodiment 27%, yet another embodiment 26%, yet another embodiment 7%, and yet another embodiment 25%.
- the content of the compound represented by the general formula (X-6-2) is an upper limit for each embodiment in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. There is a lower limit.
- the lower limit of the content is, for example, 1% of the total amount of the liquid crystal composition of the present invention in one embodiment of the present invention, 2% in another embodiment, 3% in yet another embodiment, and further 4% in another embodiment, 5% in yet another embodiment, 6% in yet another embodiment, and 8% in yet another embodiment. In still another embodiment, it is 10%.
- the upper limit of the content is, for example, 30% in one embodiment of the present invention, 20% in another embodiment, 13% in yet another embodiment, 10% in yet another embodiment, In yet another embodiment it is 7% and in yet another embodiment 3%.
- Preferred examples of the compound represented by the general formula (X-6-1) according to the present invention include at least one selected from the group consisting of the following formulas (m.1) to (m.20). .
- Preferred examples of the compound represented by the general formula (X-6-2) according to the present invention include at least one selected from the group consisting of the following formulas (m.21) to (m.28). .
- the compound represented by the general formula (M) used in the liquid crystal composition of the present invention is preferably a compound represented by the general formula (IIa).
- R 3a is an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkyl group having 2 to 8 carbon atoms.
- the methylene group in the group may be substituted with an oxygen atom unless oxygen atoms are continuously bonded, and may be substituted with a carbonyl group unless a carbonyl group is bonded continuously;
- a 2a is each independently 1,4-cyclohexylenecyclohexylene group, 1,4-phenylene group, tetrahydropyran-2,5-diyl group, dioxane-2,5-diyl group or pyrimidine-2,5- Represents a diyl group, and when A 2a represents a 1,4-phenylene group, one or more hydrogen atoms in the 1,4-phenylene group may be substituted with fluor
- m 2a is more preferably 2 , 3 or 4, more preferably m 2a is 2 or 3, and particularly preferably m 2a is 3.
- the content of the compound represented by the general formula (IIa) is an upper limit value and a lower limit value for each embodiment in consideration of properties such as solubility at low temperature, transition temperature, electrical reliability, and birefringence.
- the lower limit of the content of the compound is, for example, 2% with respect to the total amount of the liquid crystal composition of the present invention in one embodiment of the present invention, 3% in another embodiment, and 4% in yet another embodiment.
- it is 9%. 11% in yet another embodiment, 15% in yet another embodiment, and 18% in yet another embodiment.
- the upper limit of the content of the compound represented by the general formula (IIa) is, for example, 30% in one embodiment of the present invention, 20% in another embodiment, and 13% in still another embodiment. In yet another embodiment, it is 10%, in yet another embodiment 7%, and in yet another embodiment 3%.
- the compound represented by the general formula (X) is preferably a compound selected from the group represented by the general formula (XI).
- X 111 to X 117 each independently represents a fluorine atom or a hydrogen atom, at least one of X 111 to X 117 represents a fluorine atom, and R 11 represents 1 to 5 represents an alkyl group, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms, and Y 11 represents a fluorine atom or —OCF 3.
- R 11 represents 1 to 5 represents an alkyl group, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms
- Y 11 represents a fluorine atom or —OCF 3.
- the content of the compound represented by the general formula (XI) is an upper limit value and a lower limit value for each embodiment in consideration of properties such as solubility at low temperature, transition temperature, electrical reliability, and birefringence.
- the lower limit of the content is 2% with respect to the total amount of the liquid crystal composition of the present invention, 4% in another embodiment, 5% in still another embodiment, Yet another embodiment is 7%, yet another embodiment is 9%, yet another embodiment is 10%, and yet another embodiment is 12%. In still another embodiment, it is 13%. In still another embodiment, it is 15%. In yet another embodiment, it is 18%.
- the upper limit of the content is, for example, 30% in one embodiment of the present invention, 25% in another embodiment, 20% in still another embodiment, 15% in yet another embodiment, In yet another embodiment it is 10% and in yet another embodiment 5%.
- the liquid crystal composition of the present invention When used for a liquid crystal display device having a small cell gap, it is suitable to increase the content of the compound represented by the general formula (XI). When used for a liquid crystal display element with a low driving voltage, it is suitable to increase the content of the compound represented by the general formula (XI). Further, when used for a liquid crystal display element used in a low temperature environment, it is suitable to reduce the content of the compound represented by the general formula (XI). In the case of a liquid crystal composition used for a liquid crystal display device having a high response speed, it is suitable to reduce the content of the compound represented by the general formula (XI).
- the cell gap in this specification refers to an average distance between opposing alignment layers, in other words, an average thickness of a liquid crystal layer filled with a liquid crystal composition (for example, the thickness is calculated by an average of 10 points).
- the compound represented by the general formula (XI) used in the liquid crystal composition of the present invention is preferably a compound represented by the general formula (XI-1).
- R 11 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- R 11 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XI-1) is preferably 1% by mass or more, more preferably 2% by mass or more, more preferably 3% by mass or more with respect to the total amount of the liquid crystal composition of the present invention. Is more preferable, 4% by mass or more is more preferable, and 5% by mass or more is particularly preferable. In consideration of solubility at low temperature, transition temperature, electrical reliability, etc., the maximum ratio is preferably 20% by mass or less, more preferably 15% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
- the compound represented by the general formula (XI-1) used in the liquid crystal composition of the present invention is specifically a compound represented by the formula (45.1) to the formula (45.4). Among them, it is preferable to contain a compound represented by formula (45.2) to formula (45.4), and it is more preferable to contain a compound represented by formula (45.2).
- the content of the compounds represented by the above formulas (45.1) to (45.4) is preferably 1% by mass or more, and 1.5% by mass with respect to the total amount of the liquid crystal composition of the present invention.
- the above is more preferable, 2% by mass or more is further preferable, 2.5% by mass or more is further preferable, and 3% by mass or more is particularly preferable.
- the maximum ratio is preferably limited to 18% by mass or less, more preferably 15% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
- the compound represented by the general formula (X) is preferably a compound selected from the group represented by the general formula (XII).
- X 121 to X 126 each independently represents a fluorine atom or a hydrogen atom
- R 12 represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms. Or an alkoxy group having 1 to 4 carbon atoms
- Y 12 represents a fluorine atom or —OCF 3.
- the compound represented by the general formula (XII) used in the liquid crystal composition of the present invention is preferably a compound represented by the general formula (XII-1).
- R 12 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XII-1) is preferably 1% by mass or more, more preferably 2% by mass or more, more preferably 3% by mass or more with respect to the total amount of the liquid crystal composition of the present invention. Is more preferable, and 4% by mass or more is particularly preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably 15% by mass or less, more preferably 10% by mass or less, and even more preferably 8% by mass or less. 6 mass% or less is particularly preferable.
- the compound represented by the general formula (XII-1) used in the liquid crystal composition of the present invention is specifically a compound represented by the formula (46.1) to the formula (46.4). Among them, it is preferable to contain a compound represented by formula (46.2) to formula (46.4).
- the compound represented by the general formula (XII) is preferably a compound represented by the general formula (XII-2).
- R 12 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XII-2) is preferably 1% by mass or more, more preferably 3% by mass or more, with respect to the total amount of the liquid crystal composition of the present invention. Is more preferably 6% by mass or more, and particularly preferably 9% by mass or more. In consideration of solubility at low temperature, transition temperature, electrical reliability, etc., the maximum ratio is preferably 20% by mass or less, more preferably 17% by mass or less, and even more preferably 15% by mass or less. 13 mass% or less is particularly preferable.
- the compound represented by the general formula (XII-2) used in the liquid crystal composition of the present invention is specifically a compound represented by the formula (47.1) to the formula (47.4). Among them, it is preferable to contain a compound represented by formula (47.2) to formula (47.4).
- the compound represented by the general formula (M) according to the present invention is preferably, for example, a compound selected from the group of compounds represented by the general formula (VIII).
- R 8 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms
- X 81 to X 85 are Each independently represents a hydrogen atom or a fluorine atom
- Y 8 represents a fluorine atom or —OCF 3.
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types.
- they are three or more types.
- the compound represented by the general formula (VIII) is present in the liquid crystal composition, it exhibits high ⁇ n, and has an effect that the transition point can be easily controlled by adjusting the ratio with other tetracyclic compounds.
- the content of the compound represented by the general formula (VIII) is low-temperature solubility, transition temperature, electrical reliability, birefringence, process compatibility, dripping marks, It is necessary to adjust appropriately according to required performance such as image sticking and dielectric anisotropy.
- the content of the compound represented by the general formula (VIII) with respect to the total mass of the liquid crystal composition of the present invention is, for example, 1 to 25% by mass in one embodiment of the present invention. Furthermore, for example, in another embodiment of the present invention, the content of the compound is 1% to 20% by mass. For example, in still another embodiment of the present invention, the content of the compound is 1% to 15% by mass. For example, in still another embodiment of the present invention, the content of the compound is 1% to 10% by mass. For example, in still another embodiment of the present invention, the content of the compound is 1% to 7% by mass. For example, in still another embodiment of the present invention, the content of the compound is 1% to 6% by mass.
- the content of the compound is 1% to 5% by mass.
- the content of the compound is 1% to 4% by mass.
- the content of the compound is 3% to 7% by mass.
- the content of the compound is 3% to 6% by mass.
- the content of the compound is 4% to 7% by mass.
- the liquid crystal composition of the present invention maintains a low viscosity and a liquid crystal composition having a high response speed is required, it is preferable to lower the lower limit value and lower the upper limit value. Furthermore, when the liquid crystal composition of the present invention maintains a high Tni and a liquid crystal composition with good temperature stability is required, it is preferable to lower the lower limit and lower the upper limit. Further, when it is desired to increase the dielectric anisotropy in order to keep the driving voltage low, it is preferable to increase the upper limit value while increasing the lower limit value.
- the compound represented by the general formula (VIII) according to the present invention is preferably a compound represented by the general formula (VIII-1).
- R 8 has the same meaning as in general formula (VIII).
- the compound represented by the general formula (VIII-1) is specifically preferably a compound represented by the formula (26.1) to the formula (26.4), and the formula (26.1) Or the compound represented by Formula (26.2) is preferable, and the compound represented by Formula (26.2) is more preferable.
- the content of the compounds represented by the above formulas (26.1) to (26.4) is determined in consideration of the solubility at low temperature, the transition temperature, the electrical reliability, the birefringence, etc.
- the content is preferably 1% by mass or more and 20% by mass or less, more preferably 1% by mass or more and 15% by mass or less, still more preferably 1% by mass or more and 10% by mass or less, and more preferably 1% by mass or more.
- the mass% is preferably 7% by mass or less. Among these, for example, 1% by mass to 6% by mass, 1% by mass to 5% by mass, 3% by mass to 7% by mass, 3% by mass to 6% by mass, 4% by mass to 7% by mass The following is preferable.
- the compound represented by the general formula (VIII) according to the present invention is preferably a compound represented by the general formula (VIII-2).
- R 8 represents the same meaning as in general formula (VIII).
- R 8 represents the same meaning as in general formula (VIII).
- types of compounds that can be combined as the general formula (VIII-2) are appropriately combined according to desired performance such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Or in another embodiment of this invention, they are three or more types.
- the content of the compound represented by the general formula (VIII-2) is the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, transition temperature, electrical reliability, birefringence, and the like. Is preferably 2.5% by mass or more and 25% by mass or less, more preferably 8% by mass or more and 25% by mass or less, and preferably 10% by mass or less and 20% by mass or less. It is preferable that it is 15 mass% or less.
- the compound represented by the general formula (VIII-2) is preferably a compound represented by the formula (27.1) to the formula (27.4), and is represented by the formula (27.2). It is preferable that it is a compound.
- the compound represented by the general formula (M) according to the present invention is preferably a compound selected from, for example, a compound group represented by the general formula (IX).
- R 9 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms
- X 91 and X 92 are Each independently represents a hydrogen atom or a fluorine atom
- Y 9 represents a fluorine atom, a chlorine atom or —OCF 3
- U 9 represents a single bond, —COO— or —CF 2 O—.
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, it is two or more types.
- the content of the compound represented by the general formula (VIII-3) is the total mass of the liquid crystal composition of the present invention in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like. Is preferably 0.5% by mass or more and 15% by mass or less, preferably 0.5% by mass or more and 10% by mass or less, and more preferably 0.5% by mass or less and 5% by mass or less. It is preferable that they are 1 mass% or more and 5 mass% or less.
- the liquid crystal composition of the present invention maintains a low viscosity and a liquid crystal composition having a high response speed is required, it is preferable to lower the lower limit value and lower the upper limit value. Furthermore, when the liquid crystal composition of the present invention requires a high Tni and a liquid crystal composition that does not easily cause burn-in, it is preferable to lower the lower limit and lower the upper limit. Further, when it is desired to increase the dielectric anisotropy in order to keep the driving voltage low, it is preferable to increase the upper limit value while increasing the lower limit value.
- the compound represented by the general formula (IX) according to the present invention is preferably a compound represented by the general formula (IX-1).
- the compound represented by the general formula (IX-1) according to the present invention is preferably a compound represented by the general formula (IX-1-1).
- R 9 has the same meaning as in general formula (IX).
- the kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of this invention, they are three or more types.
- the content of the compound represented by the general formula (IX-1-1) is appropriately adjusted according to the embodiment in consideration of solubility at a low temperature, transition temperature, electrical reliability, birefringence, and the like.
- the content of the compound represented by the general formula (IX-1-1) is 1 to 30% by mass with respect to the total mass of the liquid crystal composition of the present invention. .
- the content of the compound is 2% to 25% by mass.
- the content of the compound is 3% to 20% by mass.
- the content of the compound is 9% to 15% by mass.
- the content of the compound is 12% to 20% by mass.
- the compound represented by the general formula (IX-1-1) is preferably a compound represented by the formula (28.1) to the formula (28.5), and the formula (28.3) or / And a compound represented by formula (28.5).
- the compound represented by the general formula (IX-1) according to the present invention is preferably a compound represented by the general formula (IX-1-2).
- R 9 represents the same meaning as in general formula (IX).
- the content of the compound represented by the general formula (IX-1-2) is based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, transition temperature, electrical reliability, and the like. On the other hand, it is preferably 1% by mass or more and 30% by mass or less, preferably 5% by mass or more and 25% by mass or less, and more preferably 8% by mass or more and 20% by mass or less.
- the compound represented by the general formula (IX-1-2) is preferably a compound represented by the formula (29.1) to the formula (29.4), and the formula (29.2) or / And a compound represented by Formula (29.4).
- the compound represented by the general formula (IX) is preferably a compound represented by the general formula (IX-2).
- the compound represented by the general formula (IX-2) according to the present invention is preferably a compound represented by the general formula (IX-2-1).
- R 9 has the same meaning as in general formula (IX).
- the content of the compound represented by the general formula (IX-2-1) is 1 to 25% by mass with respect to the total mass of the liquid crystal composition of the present invention. is there.
- the content of the compound is 1-20% by mass.
- the content of the compound is 1% to 15% by mass.
- the content of the compound is 1% to 10% by mass.
- the content of the compound is 1% to 5% by mass.
- the content of the compound is 1% to 4% by mass.
- the compound represented by the general formula (IX-2-1) is preferably a compound represented by the formula (30.1) to the formula (30.4), from the formula (30.1) It is preferable that it is a compound represented by Formula (30.2).
- the compound represented by the general formula (IX-2) according to the present invention is preferably a compound represented by the general formula (IX-2-2).
- R 9 represents the same meaning as in general formula (IX).
- the content of the compound represented by the general formula (IX-2-2) is appropriately determined for each embodiment in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. Adjusted.
- the content of the compound represented by the general formula (IX-2-2) with respect to the total mass of the liquid crystal composition of the present invention is 1 to 30% by mass in one embodiment of the present invention, and another embodiment. 1 to 25% by weight, yet another embodiment 1 to 20% by weight, yet another embodiment 1 to 17% by weight, yet another embodiment 1 to 16% by weight, yet another embodiment 1 -12% by weight, yet another embodiment 1-11% by weight, yet another embodiment 1-10% by weight, yet another embodiment 1-9% by weight, yet another embodiment.
- the compound represented by the general formula (IX-2-2) is preferably a compound represented by the formula (31.1) to the formula (31.4), from the formula (31.1) It is preferable that it is a compound represented by Formula (31.4).
- the compound represented by the general formula (IX-2) is preferably a compound represented by the general formula (IX-2-3).
- R 9 represents the same meaning as in the general formula (IX).
- the content of the compound represented by the general formula (IX-2-3) is based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, transition temperature, electrical reliability, and the like. On the other hand, it is preferably 1% by mass to 30% by mass, more preferably 3% by mass to 20% by mass, further preferably 6% by mass to 15% by mass, and more preferably 8% by mass to 10% by mass. Further preferred.
- the compound represented by the general formula (IX-2-3) is preferably a compound represented by the formula (32.1) to the formula (32.4), and the formula (32.2) and A compound represented by the formula (32.4) is preferable.
- the compound represented by the general formula (IX-2) according to the present invention is preferably a compound represented by the general formula (IX-2-4).
- R 9 represents the same meaning as in general formula (IX).
- the content of the compound represented by the general formula (IX-2-4) is based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, transition temperature, electrical reliability, and the like. On the other hand, it is preferably 1% by mass to 25% by mass, preferably 1% by mass to 20% by mass, preferably 1% by mass to 15% by mass, and preferably 1% by mass to 12% by mass, 5 mass% or more and 12 mass% or less are preferable, and 7 mass% or more and 12 mass% or less are preferable.
- the compound represented by the general formula (IX-2-4) is preferably a compound represented by the formula (33.1) to the formula (33.8), the formula (33.1), the formula More preferred are compounds represented by (33.8) and formulas (33.2) to (33.5).
- R 25 is preferably an alkenyl group having 2 to 6 carbon atoms.
- the compound represented by the general formula (IX-2) according to the present invention is preferably a compound represented by the general formula (IX-2-5).
- R 9 has the same meaning as in general formula (IX).
- R 9 has the same meaning as in general formula (IX).
- the content of the compound represented by the general formula (IX-2-5) is appropriately determined for each embodiment in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. Adjusted.
- the content of the compound represented by the general formula (IX-2-5) is 0.1 to 30% by mass in one embodiment of the present invention with respect to the total mass of the liquid crystal composition of the present invention.
- the content of the compound represented by the general formula (IX-2-5) is 0.1 to 30% by mass in one embodiment of the present invention with respect to the total mass of the liquid crystal composition of the present invention.
- the content of the compound represented by the general formula (IX-2-5) is 0.1 to 30% by mass in one embodiment of the present invention with respect to the total mass of the liquid crystal composition of the present invention.
- In another embodiment 0.3 to 25% by weight in yet another embodiment 0.5 to 20% by weight, in yet another embodiment 1 to 15% by weight, and in yet another embodiment 2 to 14 wt%, in yet another embodiment 2.5 to 15 wt%, and in yet another embodiment 3 to 12 wt%.
- the liquid crystal composition of the present invention maintains a low viscosity and a liquid crystal composition having a high response speed is required, it is preferable to lower the lower limit value and lower the upper limit value. Furthermore, when the liquid crystal composition of the present invention requires a high Tni and a liquid crystal composition that does not easily cause burn-in, it is preferable to lower the lower limit and lower the upper limit. Further, when it is desired to increase the dielectric anisotropy in order to keep the driving voltage low, it is preferable to increase the upper limit value while increasing the lower limit value.
- the compound represented by the general formula (IX-2-5) is preferably a compound represented by the formula (34.1) to the formula (34.5), and the formula (34.1), the formula A compound represented by (34.2), formula (34.3) and / or formula (34.5) is preferable.
- the compound represented by the general formula (IX) according to the present invention is preferably a compound represented by the general formula (IX-3).
- R 9 , X 91 and X 92 represent the same meaning as in the general formula (IX).
- the compound represented by the general formula (IX-3) is preferably a compound represented by the general formula (IX-3-1).
- R 9 has the same meaning as in general formula (IX).
- the content of the compound represented by the general formula (IX-3-1) is based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, transition temperature, electrical reliability, and the like. On the other hand, it is preferably 3% by mass or more and 30% by mass or less, preferably 7% by mass or more and 30% by mass or less, preferably 13% by mass or more and 20% by mass or less, and more preferably 15% by mass or more and 18% by mass or less.
- the compound represented by the general formula (IX-3-1) is preferably a compound represented by the formula (35.1) to the formula (35.4), and the formula (35.1) and / or Or it is preferable that it is a compound represented by Formula (35.2).
- the compound represented by the general formula (M) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (XIII).
- X 131 to X 135 each independently represents a fluorine atom or a hydrogen atom
- R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or Represents an alkoxy group having 1 to 4 carbon atoms
- Y 13 represents a fluorine atom or —OCF 3.
- the content of the compound represented by the general formula (XIII) has an upper limit value and a lower limit value for each embodiment in consideration of properties such as solubility at low temperature, transition temperature, electrical reliability, and birefringence. is there.
- the lower limit of the content is 2% with respect to the total amount of the liquid crystal composition of the present invention, 4% in another embodiment, 5% in still another embodiment, Yet another embodiment is 7%, yet another embodiment is 9%, yet another embodiment is 11%, and yet another embodiment is 13%. In yet another embodiment, it is 14%. In still another embodiment, it is 16%. In still another embodiment, it is 20%.
- the upper limit of the content is, for example, 30% in one embodiment of the present invention, 25% in another embodiment, 20% in still another embodiment, 15% in yet another embodiment, In yet another embodiment it is 10% and in yet another embodiment 5%.
- the liquid crystal composition of the present invention When used for a liquid crystal display device having a small cell gap, it is suitable to increase the content of the compound represented by the general formula (XIII). When used for a liquid crystal display element having a low driving voltage, it is suitable to increase the content of the compound represented by the general formula (XIII). In addition, when used for a liquid crystal display element used in a low temperature environment, it is suitable to reduce the content of the compound represented by the general formula (XIII). In the case of a liquid crystal composition used for a liquid crystal display device having a high response speed, it is suitable to reduce the content of the compound represented by the general formula (XIII).
- the compound represented by the general formula (XIII) according to the present invention is preferably a compound represented by the general formula (XIII-1).
- R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the compound represented by the general formula (XIII-1) is preferably contained in an amount of 1% by mass or more, more preferably 3% by mass or more, based on the total amount of the liquid crystal composition of the present invention, It is more preferable to contain 10% by mass or more. Moreover, as a ratio which can be contained at the maximum, 25 mass% or less is preferable, 20 mass% or less is more preferable, and 15 mass% or less is further more preferable.
- the compound represented by the general formula (XIII-1) is preferably a compound represented by the formula (48.1) to the formula (48.4), and is represented by the formula (48.2).
- a compound is preferred.
- the compound represented by the general formula (XIII) according to the present invention is preferably a compound represented by the general formula (XIII-2).
- R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the compound represented by the general formula (XIII-2) is preferably contained in an amount of 5% by mass or more, more preferably 6% by mass or more, and more preferably 8% by mass or more based on the total amount of the liquid crystal composition of the present invention. It is more preferable to contain 10% by mass or more. Moreover, as a ratio which can be contained at the maximum, 25 mass% or less is preferable, 20 mass% or less is more preferable, and 15 mass% or less is further more preferable.
- the compound represented by the general formula (XIII-2) is preferably a compound represented by the formula (49.1) to the formula (49.4), and the formula (49.1) or / and the formula A compound represented by (49.2) is preferable.
- the compound represented by the general formula (XIII) according to the present invention is preferably a compound represented by the general formula (XIII-3).
- R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the compound represented by the general formula (XIII-3) is preferably contained in an amount of 2% by mass or more, more preferably 4% by mass or more, more preferably 9% by mass or more, based on the total amount of the liquid crystal composition of the present invention. More preferably, it is more preferably 11% by mass or more. Moreover, as a ratio which can be contained at the maximum, 20 mass% or less is preferable, 17 mass% or less is more preferable, and 14 mass% or less is further more preferable.
- the compound represented by the general formula (XIII-3) is preferably a compound represented by the formula (50.1) to the formula (50.4), and the formula (50.1) or / and the formula A compound represented by (50.2) is preferred.
- the compound represented by the general formula (M) according to the present invention is preferably a compound selected from the group of compounds represented by the general formula (XIV).
- R 14 represents an alkyl group, an alkenyl group or an alkoxy group having 1 to 7 carbon atoms of 2 to 7 carbon atoms of 1 to 7 carbon atoms, and from X 141 X 144 each independently represents a fluorine atom or a hydrogen atom, Y 14 represents a fluorine atom, a chlorine atom or —OCF 3 , Q 14 represents a single bond, —COO— or —CF 2 O—, and m 14 represents 0 or 1)
- X 141 X 144 each independently represents a fluorine atom or a hydrogen atom
- Y 14 represents a fluorine atom, a chlorine atom or —OCF 3
- Q 14 represents a single bond, —COO— or —CF 2 O—
- m 14 represents 0 or 1
- the content of the compound represented by the general formula (XIV) has an upper limit value and a lower limit value for each embodiment in consideration of properties such as solubility at low temperature, transition temperature, electrical reliability, and birefringence. is there.
- the lower limit of the content is 3% with respect to the total amount of the liquid crystal composition of the present invention, 7% in another embodiment, 8% in still another embodiment, Yet another embodiment is 11%, yet another embodiment is 12%, yet another embodiment is 16%, and yet another embodiment is 18%. In still another embodiment, it is 19%. In still another embodiment, it is 22%. In still another embodiment, it is 25%.
- the upper limit of the content is, for example, 40% in one embodiment of the present invention, 35% in another embodiment, 30% in yet another embodiment, and 25% in yet another embodiment. In yet another embodiment it is 20% and in yet another embodiment it is 15%.
- the liquid crystal composition of the present invention When used for a liquid crystal display element having a low driving voltage, it is suitable to increase the content of the compound represented by the general formula (XIV). In the case of a liquid crystal composition used for a liquid crystal display device having a high response speed, it is suitable to reduce the content of the compound represented by the general formula (XIV).
- the compound represented by the general formula (XIV) according to the present invention is preferably a compound represented by the general formula (XIV-1).
- R 14 represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms, or an alkoxy group having 1 to 7 carbon atoms
- Y 14 represents fluorine.
- 1 type to 3 types in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc.
- the compound represented by the general formula (XIV-1) is preferably a compound represented by the general formula (XIV-1-1).
- R 14 represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms, or an alkoxy group having 1 to 7 carbon atoms.
- the content of the compound represented by the general formula (XIV-1) is preferably 2% by mass or more, more preferably 4% by mass or more, and more preferably 7% by mass with respect to the total amount of the liquid crystal composition of the present invention. The above is more preferable, 10% by mass or more is more preferable, and 18% by mass or more is particularly preferable.
- the maximum ratio is preferably limited to 30% by mass or less, more preferably 27% by mass or less, and more preferably 24% by mass or less. , Less than 21% by mass is particularly preferable.
- the compound represented by the general formula (XIV-1-1) is specifically preferably a compound represented by the formula (51.1) to the formula (51.4). It is more preferable to contain the compound represented by this.
- the compound represented by the general formula (XIV-1) is preferably a compound represented by the general formula (XIV-1-2).
- R 14 represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms, or an alkoxy group having 1 to 7 carbon atoms.
- the content of the compound represented by the general formula (XIV-1-2) is preferably 1% by mass or more, more preferably 3% by mass or more, more preferably 5% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is more preferable, and 7 mass% or more is particularly preferable.
- the maximum ratio is preferably 15% by mass or less, more preferably 13% by mass or less, and even more preferably 11% by mass or less. , Less than 9% by mass is particularly preferable.
- the compound represented by the general formula (XIV-1-2) is specifically preferably a compound represented by the formula (52.1) to the formula (52.4). It is preferable to contain the compound represented by 52.4).
- the compound represented by the general formula (XIV) according to the present invention is preferably a compound represented by the general formula (XIV-2).
- R 14 represents an alkyl group, an alkenyl group or an alkoxy group having 1 to 4 carbon atoms of 2 to 5 carbon atoms of 1 to 5 carbon atoms, from X 141 X 144 each independently represents a fluorine atom or a hydrogen atom, and Y 14 represents a fluorine atom, a chlorine atom or —OCF 3 )
- X 141 X 144 each independently represents a fluorine atom or a hydrogen atom
- Y 14 represents a fluorine atom, a chlorine atom or —OCF 3
- the content of the compound represented by the general formula (XIV-2) is an upper limit and a lower limit for each embodiment in consideration of properties such as solubility at low temperature, transition temperature, electrical reliability, and birefringence. There is a value.
- the lower limit of the content is 0.1% with respect to the total amount of the liquid crystal composition of the present invention, 0.5% in another embodiment, and in another embodiment. 1%, yet another embodiment is 1.2%, yet another embodiment is 1.5%, yet another embodiment is 2%, and yet another embodiment is 2.5%. . In still another embodiment, it is 3%.
- the upper limit of the content is, for example, 25% in one embodiment of the present invention, 20% in another embodiment, 15% in yet another embodiment, 10% in yet another embodiment, In yet another embodiment it is 8% and in yet another embodiment 7%.
- the liquid crystal composition of the present invention When used for a liquid crystal display element having a low driving voltage, it is suitable to increase the content of the compound represented by the general formula (XIV-2). In the case of a liquid crystal composition used for a liquid crystal display device having a high response speed, it is suitable to reduce the content of the compound represented by the general formula (XIV-2).
- the compound represented by the general formula (XIV-2) according to the present invention is preferably a compound represented by the general formula (XIV-2-1).
- R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XIV-2-1) is preferably 1% by mass or more, more preferably 3% by mass or more, with respect to the total amount of the liquid crystal composition of the present invention. % Or more is more preferable, and 7 mass% or more is particularly preferable.
- the maximum ratio is preferably 15% by mass or less, more preferably 13% by mass or less, and even more preferably 11% by mass or less. , Less than 9% by mass is particularly preferable.
- the compound represented by the general formula (XIV-2-1) is specifically preferably a compound represented by the formula (53.1) to the formula (53.4), among which the formula (53. It is preferable to contain the compound represented by 4).
- the compound represented by the general formula (XIV-2) is preferably a compound represented by the general formula (XIV-2-2).
- R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XIV-2-2) is preferably 3% by mass or more, more preferably 6% by mass or more, and more preferably 9% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is more preferable, and 12% by mass or more is particularly preferable.
- the maximum ratio is preferably 20% by mass or less, more preferably 17% by mass or less, and even more preferably 15% by mass or less. 14 mass% or less is particularly preferable.
- the compound represented by the general formula (XIV-2-2) is specifically preferably a compound represented by the formula (54.1) to the formula (54.4), among which the formula (54. It is preferable to contain the compound represented by 2) and / or Formula (54.4).
- the compound represented by the general formula (XIV-2) is preferably a compound represented by the general formula (XIV-2-3).
- R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XIV-2-3) is preferably 5% by mass or more, more preferably 9% by mass or more, and more preferably 12% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is particularly preferable.
- the maximum ratio is preferably limited to 30% by mass or less, more preferably less than 27% by mass, and even more preferably 24% by mass or less. , Less than 20% by mass is particularly preferable.
- the compound represented by the general formula (XIV-2-3) is specifically preferably a compound represented by the formula (55.1) to the formula (55.4), among which the formula (55. It is preferable to contain the compound represented by 2) and / or Formula (55.4).
- the compound represented by the general formula (XIV-2) is preferably a compound represented by the general formula (XIV-2-4).
- R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XIV-2-4) is an upper limit for each embodiment in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
- the lower limit of the content is 0.1% with respect to the total amount of the liquid crystal composition of the present invention, 0.5% in another embodiment, and in another embodiment. 0.7%, yet another embodiment is 1%, yet another embodiment is 1.2%, yet another embodiment is 1.8%, and yet another embodiment is 2%. .
- it is 2.5%.
- it is 3%.
- the upper limit of the content is, for example, 15% in one embodiment of the present invention, 12% in another embodiment, 11% in still another embodiment, 10% in yet another embodiment, In yet another embodiment it is 8%, and in yet another embodiment 6%.
- the upper limit of the content is, for example, 35% in one embodiment of the present invention, 30% in another embodiment, 25% in still another embodiment, and 20% in yet another embodiment. In yet another embodiment it is 15% and in yet another embodiment 10%.
- liquid crystal composition of the present invention When used for a liquid crystal display device having a low driving voltage, it is suitable to increase the content of the compound represented by the general formula (XIV-2-4). In the case of a liquid crystal composition used for a liquid crystal display device having a high response speed, it is suitable to reduce the content of the compound represented by the general formula (XIV-2-4).
- the compound represented by the general formula (XIV-2-4) is specifically preferably a compound represented by the formula (56.1) to the formula (56.4), among which the formula (56. It is preferable to contain the compound represented by 1), Formula (56.2), and Formula (56.4).
- the compound represented by the general formula (XIV-2) is preferably a compound represented by the general formula (XIV-2-5).
- R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XIV-2-5) is preferably 5% by mass or more, more preferably 10% by mass or more, and more preferably 13% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is particularly preferable.
- the maximum ratio is preferably limited to 25% by mass or less, more preferably less than 22% by mass, and even more preferably 18% by mass or less. , Less than 15% by mass is particularly preferable.
- the compound represented by the general formula (XIV-2-5) is specifically a compound represented by the formula (57.1) to the formula (57.4). Among these, it is preferable to contain a compound represented by the formula (57.1).
- the compound represented by the general formula (XIV-2) is preferably a compound represented by the general formula (XIV-2-6).
- R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.
- the content of the compound represented by the general formula (XIV-2-6) is preferably 5% by mass or more, more preferably 10% by mass or more, and more preferably 15% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is particularly preferable.
- the maximum ratio is preferably limited to 25% by mass or less, more preferably 22% by mass or less, and even more preferably 20% by mass or less. , Less than 17% by mass is particularly preferable.
- the compound represented by the general formula (XIV-2-6) is specifically preferably a compound represented by the formula (58.1) to the formula (58.4), among which the formula (58. It is preferable to contain the compound represented by 2).
- the compound used in the present invention does not have a peracid (—CO—OO—) structure in the molecule.
- a compound having a carbonyl group when importance is attached to the reliability and long-term stability of the liquid crystal composition, it is preferable not to use a compound having a carbonyl group.
- a compound in which a chlorine atom is substituted when importance is attached to stability by UV irradiation, it is desirable not to use a compound in which a chlorine atom is substituted. It is also preferable that only the compounds in which all the ring structures in the molecule are 6-membered rings.
- a preferred embodiment of the liquid crystal composition according to the present invention is represented by the general formula (i):
- R i1 and R i2 each independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or an alkyl group having 1 to 10 carbon atoms.
- R 1 represents an alkenyl group having 2 to 10 carbon atoms
- R 2 represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a hydrogen atom, a fluorine atom, a cyano group, —CF 3
- Ring A and Ring B are each independently (A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and , (B) a 1,4-phenylene group (one —CH ⁇ present in this group or at least two non-adjacent —CH ⁇ may be replaced by —N ⁇ ),
- Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atom or a chlorine atom
- n represents an alkenyl group having 2 to 10
- R 11 and R 12 are each independently an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl having 2 to 8 carbon atoms. And one or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group.
- the methylene group may be substituted with an oxygen atom unless oxygen atoms are continuously bonded, and may be substituted with a carbonyl group unless a carbonyl group is bonded continuously. With one or more, And a dielectric anisotropy at 25 ° C. of greater than 0 and 5 or less.
- liquid crystal composition according to the present invention, at least one compound selected from the compound group represented by the general formula (i) as the first component and the compound group represented by the general formula (M-1)
- a liquid crystal composition having a small dielectric anisotropy that is effective for lowering the capacitance of the liquid crystal layer is suitable for physical properties such as low viscosity, high compatibility, and high nematic upper limit. It can be obtained without impairing the temperature range or the like.
- the nonpolar component includes a group consisting of compounds represented by general formula (I-4), general formula (I-5), general formula (II-2) and general formula (II-3).
- the polar component may include at least one compound selected from general formula (X-2), general formula (X-3), general formula (X-5), general formula (VIII), and general formula It may contain at least one compound selected from the group consisting of compounds represented by formula (XI).
- At least one compound selected from the group of compounds represented by general formula (i) and general formula (M-1) is contained in an amount of 1 to 80% by mass in the entire liquid crystal composition. It is preferably 2 to 70% by mass, more preferably 3 to 65% by mass, still more preferably 4 to 60% by mass, and even more preferably 5 to 55%. It is particularly preferable that it is contained by mass%.
- liquid crystal composition is a liquid crystal composition comprising a compound represented by general formula (i), general formula (M-1) and general formula (I-1),
- the dielectric anisotropy at 25 ° C. is preferably greater than 0 and 5 or less, more preferably the dielectric anisotropy at 25 ° C. is greater than 0 and 4 or less, and the dielectric anisotropy at 25 ° C. Is more preferably greater than 0 and less than or equal to 3.
- liquid crystal composition is a liquid crystal composition
- a liquid crystal composition comprising a compound represented by general formula (i), general formula (M-1) and general formula (I-1)
- these three kinds of compounds are contained in an amount of 1 to 95 mass in the whole liquid crystal composition. %, Preferably 3 to 92% by mass, more preferably 5 to 90% by mass, and still more preferably 8 to 88% by mass.
- the content is preferably 10 to 85% by mass.
- Preferred embodiments of the liquid crystal composition according to the present invention include at least one compound selected from the group of compounds represented by general formula (i), general formula (M-1), general formula (L), and general formula (M).
- the compound of which type is selected is preferably contained in an amount of 50 to 100% by mass, more preferably 55 to 98% by mass, and more preferably 60 to 95% by mass in the entire liquid crystal composition. More preferably, the content is 65 to 90% by mass, still more preferably 68 to 85% by mass.
- At least one kind is selected from each of the compound groups represented by the general formula (i), the general formula (M-1), and the general formula (L).
- the compound is preferably contained in an amount of 40 to 100% by mass, more preferably 50 to 93% by mass, and further preferably 55 to 88% by mass in the total liquid crystal composition.
- the content is more preferably 58 to 85% by mass, and particularly preferably 60 to 82% by mass.
- At least one kind is selected from the compound group represented by the general formula (i), the general formula (M-1), and the general formula (M).
- the compound is preferably contained in an amount of 20 to 90% by mass, more preferably 30 to 80% by mass, and further preferably 35 to 75% by mass in the entire liquid crystal composition. 40 to 70% by mass is more preferable, and 45 to 60% by mass is particularly preferable.
- the content of a compound having a 2-methylbenzene-1,4-diyl group in the molecule, in which a hydrogen atom may be substituted with a halogen may be reduced.
- the content of the compound having a 2-methylbenzene-1,4-diyl group in the molecule is preferably 10% by mass or less, and preferably 5% by mass or less based on the total mass of the composition. Is more preferable, and it is still more preferable not to contain substantially.
- the content of the compound having a cyclohexenylene group as a ring structure is determined based on the total mass of the composition.
- the content is preferably 10% by mass or less, more preferably 5% by mass or less, and still more preferably substantially not contained.
- the liquid crystal composition of the present invention has a dielectric anisotropy ( ⁇ ) at 25 ° C. of greater than 0 and less than or equal to +5, preferably +0.5 to +4.0, more preferably +1.0 to +3.5, +1.5 to +3.0 is particularly preferred.
- the liquid crystal composition of the present invention has a refractive index anisotropy ( ⁇ n) at 25 ° C. of 0.06 to 0.20, more preferably 0.07 to 0.18, and 0.08 to 0.16. Particularly preferred. More specifically, when it corresponds to a thin cell gap, it is preferably 0.11 to 0.14, and when it corresponds to a thick cell gap, it is preferably 0.08 to 0.11.
- the liquid crystal composition of the present invention has a nematic phase-isotropic liquid phase transition temperature (T ni ) of 60 ° C. to 120 ° C., more preferably 70 ° C. to 110 ° C., and particularly preferably 70 ° C. to 100 ° C.
- T ni nematic phase-isotropic liquid phase transition temperature
- the liquid crystal composition of the present invention has a viscosity ( ⁇ ) at 25 ° C. of 5 to 20 mPa ⁇ s, more preferably 18 mPa ⁇ s or less, and particularly preferably 15 mPa ⁇ s or less.
- the liquid crystal composition of the present invention has a rotational viscosity ( ⁇ 1 ) at 25 ° C. of 20 to 60 mPa ⁇ s, more preferably 50 mPa ⁇ s or less, and particularly preferably 40 mPa ⁇ s or less.
- the polymerizable compound contained in the liquid crystal composition is polymerized by ultraviolet irradiation so that liquid crystal alignment ability is imparted, and light transmission is performed using the birefringence of the liquid crystal composition. It is preferably used for a liquid crystal display element that controls the amount of light.
- the liquid crystal composition according to the present invention may contain a polymerizable compound in order to produce a liquid crystal display device such as a PSA mode or a transverse electric field type PSA mode.
- a polymerizable compound that can be used include a photopolymerizable monomer that undergoes polymerization by energy rays such as light.
- the structure has, for example, a liquid crystal skeleton in which a plurality of six-membered rings such as biphenyl derivatives and terphenyl derivatives are connected. Examples thereof include a polymerizable compound. More specifically, a bifunctional monomer represented by the general formula (XX) is preferable.
- X 201 and X 202 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms (methyl group, ethyl group, propyl group), Sp 201 and Sp 202 each independently represent a single bond, an alkylene group having 1 to 8 carbon atoms or —O— (CH 2 ) S — (wherein s represents an integer of 2 to 7, Represents an aromatic ring)), Z 201 represents —OCH 2 —, —CH 2 O—, —COO—, —OCO—, —CF 2 O—, —OCF 2 —, —CH 2 CH 2 —, —CF 2 CF 2 —, —CH ⁇ CH—COO—, —CH ⁇ CH—OCO—, —COO—CH ⁇ CH—, —OCO—CH ⁇ CH—, —COO—CH 2 CH 2 —, —OCO—CH 2 CH 2 —, —CH 2 CH 2 —, —CH 2 CH 2
- diacrylate derivatives X 201 and X 202 is representative of a both hydrogen atoms, both preferably of dimethacrylate derivatives with X 201 and X 202 are both methyl and one Also preferred are compounds which represent a hydrogen atom and the other represents a methyl group.
- the polymerization rate of these compounds is that the diacrylate derivative is the fastest, the diacrylate derivative is slow, and the asymmetric compound is intermediate, and a preferred embodiment can be used depending on the application.
- a dimethacrylate derivative is particularly preferable.
- Sp 201 and Sp 202 each independently represent a single bond, an alkylene group having 1 to 8 carbon atoms, or —O— (CH 2 ) s —, but at least one of them is a single bond in a PSA display element.
- a compound in which both represent a single bond or one in which one represents a single bond and the other represents an alkylene group having 1 to 8 carbon atoms or —O— (CH 2 ) s — is preferable.
- an alkylene group having 1 to 4 carbon atoms is more preferable, and s is preferably 1 to 4.
- Z 201 represents —OCH 2 —, —CH 2 O—, —COO—, —OCO—, —CF 2 O—, —OCF 2 —, —CH 2 CH 2 —, —CF 2 CF 2 —, or A single bond is preferable, —COO—, —OCO—, or a single bond is more preferable, and a single bond is particularly preferable.
- M 201 represents a 1,4-phenylene group, a trans-1,4-cyclohexylene group, or a single bond in which any hydrogen atom may be substituted with a fluorine atom, and any hydrogen atom is a fluorine atom
- a 1,4-phenylene group or a single bond which may be substituted with is preferable.
- Z 201 is preferably a linking group other than a single bond, and when M 201 is a single bond, Z 201 is preferably a single bond.
- the ring structure between Sp 201 and Sp 202 is specifically preferably a structure of formula (XXa-1) to formula (XXa-5) described below.
- both ends of the bond are bonded to Sp 201 or Sp 202 .
- Polymerizable compounds containing these skeletons are optimal for PSA-type liquid crystal display elements because of their ability to regulate alignment after polymerization, and display alignment is suppressed, or display unevenness is suppressed or does not occur at all.
- the polymerizable compound is preferably at least one compound selected from the group of compounds represented by general formula (XX-1) to general formula (XX-4), among which general formula (XX -2) is more preferable.
- Sp 20 represents an alkylene group having 2 to 5 carbon atoms.
- the polymerization proceeds even when no polymerization initiator is present, but may contain a polymerization initiator in order to promote the polymerization.
- the polymerization initiator include benzoin ethers, benzophenones, acetophenones, benzyl ketals, acylphosphine oxides, and the like.
- the liquid crystal composition according to the present invention can further contain a compound represented by the general formula (Q) as an antioxidant.
- RQ is preferably an alkyl group having 1 to 22 carbon atoms or an alkoxy group, and the alkyl group (including the alkyl group in the alkoxy group) is linear or branched It may be a chain.
- the RQ represents a linear or branched alkyl group having 1 to 22 carbon atoms or a linear or branched alkoxy group, and one or more of the alkyl groups (including the alkyl group in the alkoxy group).
- the CH 2 group is —O—, —CH ⁇ CH—, —CO—, —OCO—, —COO—, —C ⁇ C—, —CF 2 O—, —OCF so that the oxygen atom is not directly adjacent.
- R Q in the general formula (Q) is a number of 1 to 20 carbon atoms, a straight-chain alkyl groups, linear alkoxy groups, one CH 2 group has been replaced -OCO- or -COO- in
- the alkyl group is at least one selected from the group consisting of a linear alkyl group, a branched alkyl group, a branched alkoxy group and a branched alkyl group in which one CH 2 group is substituted with —OCO— or —COO—.
- a linear alkyl group having 1 to 10 carbon atoms a linear alkyl group in which one CH 2 group is substituted by —OCO— or —COO—, a branched alkyl group, a branched alkoxy group, and one CH 2 group More preferred is at least one selected from the group consisting of a branched alkyl group substituted with —OCO— or —COO—.
- MQ represents a trans-1,4-cyclohexylene group, a 1,4-phenylene group or a single bond, and a trans-1,4-cyclohexylene group or a 1,4-phenylene group is preferred.
- the compound represented by the general formula (Q) is preferably at least one compound selected from the group of compounds represented by the following general formulas (Qa) to (Qd):
- the compound represented by the general formula (Qa) and / or (Qc) is more preferable.
- R Q1 is preferably a linear alkyl group having 1 to 10 carbon atoms or a branched alkyl group
- R Q2 is a straight chain having 1 to 20 carbon atoms.
- a chain alkyl group or a branched chain alkyl group is preferable
- R Q3 is preferably a linear alkyl group having 1 to 8 carbon atoms, a branched chain alkyl group, a linear alkoxy group or a branched chain alkoxy group, and L Q is 1 carbon atom.
- a linear alkylene group or a branched alkylene group of 8 to 8 is preferred.
- the compound represented by the general formula (Q) is more preferably a compound represented by the following formula (Qa-1) and / or (Qc-1).
- the compound represented by the general formula (Q) preferably contains one or two compounds, more preferably contains one to five compounds, and the content is It is preferably 0.001 to 1% by mass, preferably 0.001 to 0.1% by mass, and 0.001 to 0.05% by mass with respect to the total mass of the liquid crystal composition of the present invention. It is preferable that
- the second aspect of the present invention is a liquid crystal display device comprising a liquid crystal composition containing the compound represented by the general formula (i) and having a dielectric anisotropy at 25 ° C. of greater than 0 and 5 or less.
- the liquid crystal display device includes a compound represented by general formula (i) and a compound represented by general formula (M-1), and has a dielectric anisotropy at 25 ° C. of more than 0 and 5 It is preferable to provide the following liquid crystal composition.
- the liquid crystal display element according to the present invention is useful for an AM-LCD (active matrix liquid crystal display element) and can be used for a transmissive or reflective liquid crystal display element. Further, as a driving method (or mode) of the liquid crystal display element according to the present invention, ECB-LCD, VA-LCD, VA-IPS-LCD, FFS (fringe field switching) -LCD, TN (nematic) It is useful for liquid crystal display elements), STN-LCDs (super twisted nematic liquid crystal display elements), OCB-LCDs and IPS-LCDs (in-plane switching liquid crystal display elements), but IPS mode or FFS mode liquid crystal display elements are particularly preferred. .
- Liquid crystal displays used in portable tablets such as smartphones in recent years are mainly developed because low power consumption is important in horizontal electric field type liquid crystal displays such as IPS mode and FFS mode, which have been rapidly developed and popularized.
- a liquid crystal composition having a high ⁇ and positive dielectric anisotropy is preferably used.
- the viscosity of the liquid crystal itself tends to be high, and time loss due to charging not only the liquid crystal layer but also the FFS substrate insulating layer (for example, the insulating layer 18 in FIGS. 5 and 7 described later) is likely to occur.
- the response speed is not enough.
- the induced polarization of the liquid crystal layer can be reduced by reducing the capacitance of the liquid crystal layer, that is, by using a liquid crystal composition having a very small ⁇ .
- the viscosity of the liquid crystal composition itself is also reduced, and an extremely fast response speed can be achieved in the IPS and FFS modes.
- the two substrates of the liquid crystal cell used in the liquid crystal display element can be made of a transparent material having flexibility such as glass or plastic, and one of them can be an opaque material such as silicon.
- a transparent substrate having a transparent electrode layer can be obtained, for example, by sputtering indium tin oxide (ITO) on a transparent substrate such as a glass plate.
- the color filter can be produced by, for example, a pigment dispersion method, a printing method, an electrodeposition method, or a dyeing method.
- a method for producing a color filter by a pigment dispersion method will be described as an example.
- a curable coloring composition for a color filter is applied on the transparent substrate, subjected to patterning treatment, and cured by heating or light irradiation. By performing this process for each of the three colors red, green, and blue, a pixel portion for a color filter can be manufactured.
- a pixel electrode provided with an active element such as a TFT or a thin film diode may be provided on the substrate.
- the substrate is opposed so that the transparent electrode layer is on the inside.
- the thickness of the light control layer (liquid crystal layer) to be obtained is 1 to 100 ⁇ m. More preferably, the thickness is 1.5 to 10 ⁇ m.
- the polarizing plate it is preferable to adjust the product of the refractive index anisotropy ⁇ n of the liquid crystal and the cell thickness G so that the contrast is maximized.
- the polarizing axis of each polarizing plate can be adjusted so that the viewing angle and contrast are good.
- a retardation film for widening the viewing angle can also be used.
- the spacer include columnar spacers made of glass particles, plastic particles, alumina particles, a photoresist material, and the like.
- a sealant such as an epoxy thermosetting composition is screen-printed on the substrates with a liquid crystal inlet provided, the substrates are bonded together, and heated to thermally cure the sealant.
- a normal vacuum injection method or an ODF method can be used as a method of sandwiching the liquid crystal composition (containing a polymerizable compound as necessary) between the two substrates.
- a vacuum injection method there is a problem that an injection mark remains instead of a drop mark.
- it can use more suitably for the display element manufactured using ODF method.
- a sealant such as epoxy photothermal curing is drawn on a backplane or frontplane substrate using a dispenser in a closed-loop bank shape, and then removed.
- a liquid crystal display element can be manufactured by bonding a front plane and a back plane after dropping a predetermined amount of the liquid crystal composition in the air.
- the liquid crystal composition of the present invention can be preferably used because the liquid crystal composition can be stably dropped in the ODF process.
- an appropriate polymerization rate is desirable in order to obtain good alignment performance of liquid crystals. Therefore, active energy rays such as ultraviolet rays or electron beams are irradiated singly or in combination or sequentially.
- the method of polymerizing by is preferred.
- ultraviolet rays When ultraviolet rays are used, a polarized light source or a non-polarized light source may be used.
- the polymerization is performed in a state where the polymerizable compound-containing liquid crystal composition is sandwiched between two substrates, at least the substrate on the irradiation surface side must be given appropriate transparency to the active energy rays. I must.
- the orientation state of the unpolymerized part is changed by changing conditions such as an electric field, a magnetic field, or temperature, and further irradiation with active energy rays is performed. Then, it is possible to use a means for polymerization.
- a means for polymerization In particular, when ultraviolet exposure is performed, it is preferable to perform ultraviolet exposure while applying an alternating electric field to the polymerizable compound-containing liquid crystal composition.
- the alternating electric field to be applied is preferably an alternating current having a frequency of 10 Hz to 10 kHz, more preferably a frequency of 60 Hz to 10 kHz, and the voltage is selected depending on a desired pretilt angle of the liquid crystal display element.
- the pretilt angle of the liquid crystal display element can be controlled by the applied voltage.
- the pretilt angle is preferably controlled from 80 degrees to 89.9 degrees from the viewpoint of alignment stability and contrast.
- the temperature during irradiation is preferably within a temperature range in which the liquid crystal state of the liquid crystal composition of the present invention is maintained. Polymerization is preferably performed at a temperature close to room temperature, that is, typically at a temperature of 15 to 35 ° C.
- a lamp for generating ultraviolet rays a metal halide lamp, a high-pressure mercury lamp, an ultra-high pressure mercury lamp, or the like can be used.
- a wavelength of the ultraviolet-rays to irradiate it is preferable to irradiate the ultraviolet-ray of the wavelength range which is not the absorption wavelength range of a liquid crystal composition, and it is preferable to cut and use an ultraviolet-ray as needed.
- Intensity of ultraviolet irradiation is preferably from 0.1mW / cm 2 ⁇ 100W / cm 2, 2mW / cm 2 ⁇ 50W / cm 2 is more preferable.
- the amount of energy of ultraviolet rays to be irradiated can be adjusted as appropriate, but is preferably 10 mJ / cm 2 to 500 J / cm 2, and more preferably 100 mJ / cm 2 to 200 J / cm 2 .
- the intensity may be changed.
- the time for irradiating with ultraviolet rays is appropriately selected depending on the intensity of the irradiated ultraviolet rays, but is preferably from 10 seconds to 3600 seconds, and more preferably from 10 seconds to 600 seconds.
- the liquid crystal display device using the liquid crystal composition of the present invention is useful for achieving both high-speed response and suppression of display failure, and is particularly useful for a liquid crystal display device for active matrix driving, including VA mode, PSVA mode, It can be applied to liquid crystal display elements for PSA mode, IPS (in-plane switching) mode, VA-IPS mode, FFS (fringe field switching) mode or ECB mode.
- liquid crystal display element an example of a liquid crystal display
- FIG. 1 is a cross-sectional view showing a liquid crystal display element including two substrates facing each other, a sealing material provided between the substrates, and liquid crystal sealed in a sealing region surrounded by the sealing material. It is.
- the TFT layer 102 and the pixel electrode 103 are provided on the first substrate 100, the backplane on which the passivation film 104 and the first alignment film 105 are provided, and the black matrix on the second substrate 200.
- 202, a color filter 203, a planarization film (overcoat layer) 201, and a transparent electrode 204 are provided, and a second alignment film 205 is provided thereon, provided between the front plane facing the back plane and the substrate.
- a sealing material 301 and a liquid crystal layer 303 sealed in a sealing region surrounded by the sealing material, and protrusions (columnar spacers) 302 and 304 are provided on a substrate surface in contact with the sealing material 301. The specific aspect of a liquid crystal display element is shown.
- the first substrate or the second substrate is not particularly limited as long as it is substantially transparent, and glass, ceramics, plastics, or the like can be used.
- Plastic substrates include cellulose derivatives such as cellulose, triacetyl cellulose, diacetyl cellulose, polycycloolefin derivatives, polyesters such as polyethylene terephthalate and polyethylene naphthalate, polypropylene, polyethylene, etc.
- Inorganic-organic composite materials such as glass fiber-acrylic resin can be used.
- the function of the barrier film is to reduce the moisture permeability of the plastic substrate and to improve the reliability of the electrical characteristics of the liquid crystal display element.
- the barrier film is not particularly limited as long as it has high transparency and low water vapor permeability. Generally, vapor deposition, sputtering, chemical vapor deposition method (CVD method) using an inorganic material such as silicon oxide is used. ) Is used.
- the same material or different materials may be used as the first substrate or the second substrate, and there is no particular limitation.
- Use of a glass substrate is preferable because a liquid crystal display element having excellent heat resistance and dimensional stability can be manufactured.
- a plastic substrate is preferable because it is suitable for a manufacturing method using a roll-to-roll method and is suitable for weight reduction or flexibility. For the purpose of imparting flatness and heat resistance, good results can be obtained by combining a plastic substrate and a glass substrate.
- a substrate is used as the material of the first substrate 100 or the second substrate 200.
- the TFT layer 102 and the pixel electrode 103 are provided on the first substrate 100. These are manufactured by a normal array process.
- a backplane is obtained by providing a passivation film 104 and a first alignment film 105 thereon.
- a passivation film 104 (also referred to as an inorganic protective film) is a film for protecting the TFT layer.
- a nitride film (SiNx), an oxide film (SiOx), or the like is formed by a chemical vapor deposition (CVD) technique or the like.
- the first alignment film 105 is a film having a function of aligning liquid crystals, and a polymer material such as polyimide is usually used in many cases.
- a coating solution an alignment agent solution composed of a polymer material and a solvent is used. Since the alignment film may hinder the adhesive force with the sealing material, a pattern is applied in the sealing region.
- a printing method such as a flexographic printing method or a droplet discharge method such as an ink jet is used.
- the applied alignment agent solution is crosslinked and cured by baking after the solvent is evaporated by temporary drying. Thereafter, an alignment process is performed to provide an alignment function.
- Alignment treatment is usually performed by a rubbing method.
- the polymer film formed as described above is rubbed in one direction using a rubbing cloth made of fibers such as rayon, thereby producing liquid crystal alignment ability.
- a photo-alignment method is a method of generating alignment ability by irradiating polarized light on an alignment film containing an organic material having photosensitivity, and does not cause the generation of scratches or dust on the substrate due to the rubbing method.
- the organic material in the photo-alignment method include a material containing a dichroic dye.
- Dichroic dyes include molecular orientation induction or isomerization reaction (eg, azobenzene group), dimerization reaction (eg, cinnamoyl group), photocrosslinking reaction (eg, benzophenone group) due to Weigert effect resulting from photodichroism.
- a photo-alignment group that causes a photoreaction that causes liquid crystal alignment ability
- a photolysis reaction eg, polyimide group
- the applied alignment agent solution is irradiated with light having an arbitrary deflection (polarized light), whereby an alignment film having alignment ability in an arbitrary direction can be obtained.
- One front plane is provided with a black matrix 202, a color filter 203, a planarizing film 201, a transparent electrode 204, and a second alignment film 205 on a second substrate 200.
- the black matrix 202 is produced by, for example, a pigment dispersion method. Specifically, a color resin solution in which a black colorant is uniformly dispersed for forming a black matrix is applied on the second substrate 200 provided with the barrier film 201 to form a colored layer. Subsequently, the colored layer is baked and cured. A photoresist is applied on this and prebaked. After exposing the photoresist through a mask pattern, development is performed to pattern the colored layer. Thereafter, the photoresist layer is peeled off and the colored layer is baked to complete the black matrix 202.
- a color resin solution in which a black colorant is uniformly dispersed for forming a black matrix is applied on the second substrate 200 provided with the barrier film 201 to form a colored layer. Subsequently, the colored layer is baked and cured. A photoresist is applied on this and prebaked. After exposing the photoresist through a mask pattern, development is performed to pattern the colored layer. Thereafter, the photo
- a photoresist type pigment dispersion may be used.
- a photoresist-type pigment dispersion is applied, pre-baked, exposed through a mask pattern, and then developed to pattern the colored layer. Thereafter, the photoresist layer is peeled off and the colored layer is baked to complete the black matrix 202.
- the color filter 203 is produced by a pigment dispersion method, an electrodeposition method, a printing method, a dyeing method, or the like.
- a pigment dispersion method as an example, a color resin liquid in which a pigment (for example, red) is uniformly dispersed is applied onto the second substrate 200, and after baking and curing, a photoresist is applied thereon and prebaked. After the photoresist is exposed through a mask pattern, development is performed and patterning is performed. Thereafter, the photoresist layer is peeled off and baked again to complete the (red) color filter 203. There is no particular limitation on the color order to be produced. Similarly, a green color filter 203 and a blue color filter 203 are formed.
- the transparent electrode 204 is provided on the color filter 203 (if necessary, an overcoat layer (201) is provided on the color filter 203 for surface flattening).
- the transparent electrode 204 preferably has a high transmittance, and preferably has a low electrical resistance.
- the transparent electrode 204 is formed by sputtering an oxide film such as ITO.
- a passivation film may be provided on the transparent electrode 204 for the purpose of protecting the transparent electrode 204.
- the second alignment film 205 is the same as the first alignment film 105 described above.
- the shape of the columnar spacer is not particularly limited, and the horizontal cross section can be various shapes such as a circle and a polygon such as a quadrangle. A polygonal shape is particularly preferable.
- the protrusion shape is preferably a truncated cone or a truncated pyramid.
- the material of the columnar spacer is not particularly limited as long as it is a sealing material, an organic solvent used for the sealing material, or a material that does not dissolve in liquid crystal, but it may be a synthetic resin (curable resin) in terms of processing and weight reduction. preferable.
- the protrusion can be provided on the surface of the first substrate in contact with the sealing material by a photolithography method or a droplet discharge method. For these reasons, it is preferable to use a photocurable resin suitable for a photolithography method or a droplet discharge method.
- FIG. 2 is a diagram of an exposure process using a columnar spacer preparation pattern formed on a black matrix as a photomask pattern.
- a resin solution for forming columnar spacers (not containing a colorant) is applied on the transparent electrode 204 of the front plane. Subsequently, the resin layer 402 is baked and cured. A photoresist is applied on this and prebaked. After exposing the photoresist through the mask pattern 401, development is performed to pattern the resin layer. Thereafter, the photoresist layer is peeled off, and the resin layer is baked to complete columnar spacers (302 and 304 in FIG. 1).
- the formation position of the columnar spacer can be determined at a desired position by the mask pattern. Therefore, both the inside of the sealing region of the liquid crystal display element and the outside of the sealing region (sealed material application portion) can be manufactured simultaneously.
- the columnar spacer is preferably formed so as to be positioned on the black matrix so that the quality of the sealing region does not deteriorate.
- a columnar spacer manufactured by a photolithography method in this way is sometimes called a column spacer or a photospacer.
- a mixture of a negative water-soluble resin such as PVA-stilbazo photosensitive resin, a polyfunctional acrylic monomer, an acrylic acid copolymer, a triazole initiator, or the like is used.
- a color resin in which a colorant is dispersed in a polyimide resin there is no particular limitation, and a spacer can be obtained from a known material in accordance with the compatibility with the liquid crystal or the sealing material to be used.
- a sealing material (301 in FIG. 1) is applied to the surface of the backplane that contacts the sealing material.
- the material of the sealing material is not particularly limited, and a curable resin composition in which a polymerization initiator is added to an epoxy or acrylic photocurable, thermosetting, or photothermal combination curable resin is used.
- a curable resin composition in which a polymerization initiator is added to an epoxy or acrylic photocurable, thermosetting, or photothermal combination curable resin is used.
- fillers made of inorganic or organic substances may be added.
- the shape of these fillers is not particularly limited, and includes a spherical shape, a fiber shape, and an amorphous shape.
- a spherical or fibrous gap material having a monodisperse diameter is mixed, or in order to further strengthen the adhesive force with the substrate, a fibrous substance that is easily entangled with the protrusion on the substrate is used. You may mix.
- the diameter of the fibrous material used at this time is desirably about 1/5 to 1/10 or less of the cell gap, and the length of the fibrous material is desirably shorter than the seal coating width.
- the material of the fibrous substance is not particularly limited as long as a predetermined shape can be obtained, and synthetic fibers such as cellulose, polyamide, and polyester, and inorganic materials such as glass and carbon can be appropriately selected.
- the sealing material As a method for applying the sealing material, there are a printing method and a dispensing method, but a dispensing method with a small amount of the sealing material used is desirable.
- the application position of the sealing material is usually on the black matrix so as not to adversely affect the sealing area.
- the sealing material application shape is a closed loop shape.
- the liquid crystal is dropped on the closed loop shape (sealing region) of the front plane coated with the sealing material.
- a dispenser is used. Since the amount of liquid crystal to be dropped coincides with the volume of the liquid crystal cell, the amount is basically the same as the volume obtained by multiplying the height of the column spacer and the seal application area. However, in order to optimize liquid crystal leakage and display characteristics in the cell bonding process, the amount of liquid crystal to be dropped may be adjusted as appropriate, or the liquid crystal dropping position may be dispersed.
- the back plane is bonded to the front plane where the sealing material is applied and the liquid crystal is dropped.
- the front plane and the back plane are adsorbed on a stage having a mechanism for adsorbing a substrate such as an electrostatic chuck, and the second alignment film on the front plane and the first alignment film on the back plane face each other.
- it is arranged at a position (distance) where the sealing material does not contact the other substrate.
- the system is depressurized. After decompression is completed, the positions of both substrates are adjusted while confirming the bonding position between the front plane and the back plane (alignment operation).
- the substrate is brought close to a position where the sealing material on the front plane and the back plane are in contact with each other.
- the system is filled with an inert gas, and the pressure is gradually returned to normal pressure while releasing the reduced pressure.
- the front plane and the back plane are bonded together by atmospheric pressure, and a cell gap is formed at the height of the columnar spacer.
- the sealing material is irradiated with ultraviolet rays to cure the sealing material, thereby forming a liquid crystal cell.
- a heating step is added in some cases to promote curing of the sealing material. A heating process is often added to enhance the adhesive strength of the sealing material and improve the reliability of electrical characteristics.
- a second preferred embodiment of the liquid crystal display device includes a first substrate having an electrode layer including a first alignment layer and a thin film transistor on the surface, and a second substrate having a second alignment layer on the surface. Are arranged so as to face each other and the liquid crystal layer containing the liquid crystal composition is filled between the first substrate and the second substrate, and includes the thin film transistor.
- the electrode layer includes a plurality of gate wirings and data wirings arranged in a mesh pattern, a thin film transistor provided at each intersection of the gate wiring and the data wiring, a pixel electrode connected to the thin film transistor, and the pixel And a common electrode provided on the first substrate apart from the electrode.
- the first alignment layer and the second alignment layer provided in the vicinity of the liquid crystal layer are preferably alignment films that induce homogeneous alignment with respect to the liquid crystal composition.
- the liquid crystal display element includes a second polarizing plate, a second substrate, an electrode layer including a thin film transistor (also referred to as a thin film transistor layer), an alignment film, a liquid crystal layer including a liquid crystal composition, and an alignment film. It is preferable that the color filter, the first substrate, and the first polarizing plate are sequentially stacked.
- the electric field (E) generated between the common electrode and the pixel electrode can have a planar component. Therefore, for example, when an alignment film that induces homogeneous alignment with respect to the liquid crystal composition is used for the alignment layer, the alignment layer is aligned in the plane direction that is the alignment direction of the alignment film before voltage is applied between the common electrode and the pixel electrode.
- the liquid crystal molecules that block light, and when a voltage is applied, the liquid crystal molecules rotate horizontally by the electric field (E) applied in the plane direction, and can be arranged along the electric field direction to provide an element that blocks light. .
- the liquid crystal display element according to the present invention may be a so-called color filter on array (COA), or a color filter may be provided between an electrode layer including a thin film transistor and a liquid crystal layer, or the thin film transistor.
- COA color filter on array
- a color filter may be provided between the electrode layer containing and the second substrate. That is, in the configuration of the liquid crystal display element according to the invention, it is preferable that the color filter 6 is formed on the same substrate side as the first substrate on which the electrode layer 3 including a thin film transistor is formed.
- “on the substrate” in this specification includes not only a direct contact with the substrate but also a indirectly supported state in which the substrate is supported.
- Another more preferable embodiment (FFS) of the second embodiment in the liquid crystal display composition according to the present invention includes a first substrate having an electrode layer including a first alignment layer and a thin film transistor on the surface, and a second alignment layer.
- the electrode layer including the thin film transistor includes a plurality of gate wirings and data wirings arranged in a mesh pattern, a thin film transistor provided at each intersection of the gate wiring and the data wiring, and connected to the thin film transistor And a common electrode that is spaced apart from the pixel electrode and arranged in parallel on the first substrate, and the shortest separation distance between the adjacent common electrode and the pixel electrode It is preferred but shorter than the shortest distance G between the alignment layer.
- a liquid crystal display element in which the shortest separation distance d between the common electrode and the pixel electrode is longer than the shortest separation distance G between the alignment layers is referred to as an IPS liquid crystal display element.
- An element in which the shortest distance d from the electrode is shorter than the shortest distance G between the alignment layers is referred to as FFS. Accordingly, the only requirement for the FFS method is that the shortest separation distance d between the adjacent common electrode and the pixel electrode is shorter than the shortest separation distance G between the alignment layers. Therefore, the surface of the common electrode and the surface of the pixel electrode There is no limitation on the positional relationship in the thickness direction. Therefore, in the FSS mode liquid crystal display element according to the present invention, as shown in FIGS. 3 to 7, the pixel electrode may be provided on the liquid crystal layer side from the common electrode, and the pixel electrode and the common electrode are on the same plane. May be provided.
- the liquid crystal composition according to the present invention can reduce the induced polarization of the liquid crystal layer, particularly when used for a liquid crystal display element of an FFS driving system (FFS-LCD). Moreover, it is preferable from a viewpoint of a high-speed response and reduction of image sticking.
- FFS-LCD FFS driving system
- FIG. 3 is an exploded perspective view schematically showing a structure of one embodiment of the liquid crystal display element, which is a so-called FFS type liquid crystal display element.
- a liquid crystal display element 10 according to the present invention includes a second polarizing plate 8, a second substrate 7, an electrode layer (also referred to as a thin film transistor layer) 3 including a thin film transistor, an alignment film 4, and a liquid crystal composition. It is preferable that the liquid crystal layer 5, the alignment film 4, the color filter 6, the first substrate 2, and the first polarizing plate 1 are sequentially stacked. Further, as shown in FIG.
- the second substrate 7 and the first substrate 2 may be sandwiched between a pair of polarizing plates 1 and 8. Further, in FIG. 3, a color filter 6 is provided between the second substrate 7 and the alignment film 4. Further, a pair of alignment films 4 may be formed on the (transparent) electrode (layer) 3 so as to be close to the liquid crystal layer 5 according to the present invention and to directly contact the liquid crystal composition constituting the liquid crystal layer 5.
- a so-called color filter on array may be used, and the color filter 6 may be provided between the thin film transistor layer 3 and the liquid crystal layer 5.
- a color filter 6 may be provided between the thin film transistor layer 3 and the first substrate 2.
- the FFS mode liquid crystal display element uses a fringe electric field.
- the shortest separation distance d between the adjacent common electrode and the pixel electrode is shorter than the shortest separation distance G between the alignment layers, the common electrode and the pixel electrode A fringe electric field is formed between them, and the horizontal and vertical alignments of the liquid crystal molecules can be used efficiently. That is, in the case of the FFS liquid crystal display element, a horizontal electric field formed in a direction perpendicular to a line forming the comb-teeth of the pixel electrode 21 and a parabolic electric field can be used.
- FIG. 4 is an enlarged plan view of a region II of the electrode layer 3 (or also referred to as the thin film transistor layer 3) including the thin film transistor formed on the substrate in FIG.
- the thin film transistor 20 including the source electrode 27, the drain electrode 24, and the gate electrode 28 serves as a switch element that supplies a display signal to the pixel electrode 21. 21 is provided.
- FIG. 4 shows a configuration in which a flat plate-like common electrode 22 is formed on the back surface of an interdigital pixel electrode 21 via an insulating layer (not shown).
- the surface of the pixel electrode 21 may be covered with a protective insulating film and an alignment film layer.
- a storage capacitor 23 for storing a display signal supplied through the data wiring 25 may be provided in a region surrounded by the plurality of gate wirings 26 and the plurality of data wirings 25. Further, a common line 29 is provided in parallel with the gate wiring 26. The common line 29 is connected to the common electrode 22 in order to supply a common signal to the common electrode 22.
- FIG. 5 is an example of a cross-sectional view of the liquid crystal display element taken along the line III-III in FIG.
- the substrate 7 is spaced apart from the alignment layer at a predetermined gap G, and the liquid crystal layer 5 containing a liquid crystal composition is filled in this space.
- a gate insulating film 12 is formed on a part of the surface of the first substrate 2
- a common electrode 22 is formed on a part of the surface of the gate insulating film 12, and the common electrode 22 and the thin film transistor 20 are further formed.
- An insulating film 18 is formed so as to cover it.
- a pixel electrode 21 is provided on the insulating film 18, and the pixel electrode 21 is in contact with the liquid crystal layer 5 through the alignment layer 4. Therefore, the minimum distance d between the pixel electrode and the common electrode can be adjusted as the (average) film thickness of the gate insulating film 12. In other words, in the embodiment of FIG. 5, the distance in the horizontal direction on the substrate between the pixel electrode and the common electrode is zero.
- the electrode width of the comb-like portion of the pixel electrode 21: l and the width of the gap of the comb-like portion of the pixel electrode 21: m are such that all the liquid crystal molecules in the liquid crystal layer 5 can be driven by the generated electric field. It is preferable to form the width.
- the major axis direction is
- a voltage is applied to the liquid crystal molecules arranged parallel to the alignment direction of the alignment layer, an equipotential line of a parabolic electric field is formed between the pixel electrode 21 and the common electrode 22 between the pixel electrode 21 and the common electrode 22.
- the liquid crystal molecules in the liquid crystal layer 5 rotate in the liquid crystal layer 5 along the formed electric field and function as a switching element.
- the plane direction that is the alignment direction of the alignment film before voltage is applied between the common electrode and the pixel electrode
- the common electrode and the pixel electrode are separated from each other on the same substrate (or electrode layer).
- the vertical component electric field (fringe field) derived from the edges of these electrodes is generated when the shortest separation distance d between the adjacent common electrode and the pixel electrode is shorter than the shortest separation distance G between the alignment layers.
- the amount of the compound having a high dielectric anisotropy ( ⁇ ), which has a high characteristic of the liquid crystal composition itself, can be reduced as much as possible, so that the liquid crystal composition itself can contain a large amount of a low-viscosity compound. .
- the liquid crystal composition according to the present invention uses a liquid crystal molecule having a relatively low dielectric anisotropy of ⁇ of 5 or less, the major axis direction of the liquid crystal molecule is aligned along the generated electric field direction.
- liquid crystal molecules having a relatively low dielectric anisotropy with ⁇ of 5 or less can be driven from the viewpoint that a low voltage drive is possible because the distance between the electrodes is short. Therefore, superior characteristics can be obtained as compared with liquid crystal display elements of drive systems other than the FFS system using liquid crystal molecules having a large dielectric anisotropy.
- the configuration of another preferred embodiment of the second embodiment in the liquid crystal display composition according to the present invention is (FFS), a first substrate having an electrode layer including a first alignment layer and a thin film transistor on the surface, and a second A liquid crystal in which a liquid crystal layer containing a liquid crystal composition is filled between the first substrate and the second substrate.
- the electrode layer including the thin film transistor which is a display element, includes a common electrode, a plurality of gate wirings and data wirings arranged in a mesh shape, and a thin film transistor provided at each intersection of the gate wiring and the data wiring And a pixel electrode connected to the thin film transistor, and the pixel electrode is preferably provided so as to protrude from the common electrode toward the second substrate.
- the first alignment layer and the second alignment layer provided in the vicinity of the liquid crystal layer are preferably alignment films that induce homogeneous alignment with respect to the liquid crystal composition.
- FIG. 6 is another form of a plan view in which the region II of the electrode layer 3 including the thin film transistor (also referred to as the thin film transistor layer 3) formed on the substrate in FIG. 3 is enlarged.
- the thin film transistor 20 including the source electrode 27, the drain electrode 24, and the gate electrode 28 serves as a switch element that supplies a display signal to the pixel electrode 21.
- the pixel electrode 21 may have a structure cut out by at least one notch, and an example thereof is shown in FIG.
- the pixel electrode 21 has a shape in which the center and both ends of a rectangular flat plate are cut out by a triangular cutout, and the remaining region is cut out by eight rectangular cutouts.
- Reference numeral 22 denotes a comb tooth body (not shown).
- the surface of the pixel electrode may be covered with a protective insulating film and an alignment film layer.
- a storage capacitor 23 for storing a display signal supplied through the data wiring 24 may be provided in a region surrounded by the plurality of gate wirings 25 and the plurality of data wirings 24. Note that the shape and number of the notches are not particularly limited.
- FIG. 7 shows another example of the cross-sectional view of the liquid crystal display element taken along the line III-III in FIG. That is, the difference from the structure of the liquid crystal display element shown in FIG. 5 is that the liquid crystal display element shown in FIG. 5 has a common electrode as a flat plate and a pixel electrode as a comb.
- the pixel electrode 21 has a rectangular flat plate whose center and both ends are cut out by a triangular cutout, and a remaining area is 8. It has a shape cut out by two rectangular cutouts, and the common electrode has a comb-like structure.
- the minimum separation distance d between the pixel electrode and the common electrode is equal to or greater than the (average) film thickness of the gate insulating film 12 and less than the alignment layer separation distance G.
- the common electrode has a comb-like structure, but the common electrode may be a flat plate in this embodiment.
- the FFS mode liquid crystal display element according to the present invention only needs to satisfy the condition that the shortest separation distance d between the adjacent common electrode and the pixel electrode is shorter than the shortest separation distance G between the alignment layers.
- the pixel electrode 21 is covered with the protective film 18, but in the configuration of the liquid crystal display element shown in FIG. 5, the pixel electrode 21 is covered with the alignment layer 4. .
- the pixel electrode may be covered with either a protective film or an alignment film.
- a polarizing plate is formed on one surface of the first substrate 2, and a gate insulating film 12 is formed so as to cover the comb-like common electrode 22 formed on a part of the other surface.
- a pixel electrode 21 is formed on a part of the surface of the gate insulating film 12, and an insulating film 18 is formed so as to cover the pixel electrode 21 and the thin film transistor 20.
- an alignment layer 4, a liquid crystal layer 5, an alignment layer 4, a color filter 6, a second substrate 7 and a polarizing plate 8 are laminated on the insulating film 18.
- the minimum separation distance d between the pixel electrode and the common electrode is adjusted by both electrode positions, the electrode width of the comb-like portion of the pixel electrode 21: l, or the width of the gap of the comb-like portion of the pixel electrode 21: m. can do.
- an electric field (E) having a thickness direction component can be applied at the same time because an electric field having a planar direction component is formed and the height in the thickness direction is different between the surface of the pixel electrode and the surface of the common electrode.
- the FFS mode liquid crystal display element uses a fringe electric field, and is particularly limited as long as the shortest distance d between the adjacent common electrode and the pixel electrode is shorter than the shortest distance G between the alignment layers.
- the plurality of teeth of the comb-shaped pixel electrode and the plurality of teeth of the comb-shaped common electrode are provided on the substrate in a state of being separated and engaged with each other. Also good.
- a fringe electric field can be used if the distance between the teeth of the common electrode and the teeth of the pixel electrode is shorter than the shortest distance G between the alignment layers.
- the liquid crystal composition to be used can exhibit the effects of high-speed response and reduction of image sticking from the viewpoint of low ⁇ .
- the measured characteristics are as follows.
- Tni Nematic phase-isotropic liquid phase transition temperature (° C) ⁇ n: Refractive index anisotropy at 295K (also known as birefringence) ⁇ : Dielectric anisotropy at 295K ⁇ : Viscosity at 295K (mPa ⁇ s) ⁇ 1: rotational viscosity at 295 K (mPa ⁇ s) VHR: Voltage holding ratio (%) at 313K under conditions of frequency 60Hz and applied voltage 5V Burn-in: The burn-in evaluation of the liquid crystal display element is based on the following four-step evaluation of the afterimage level of the fixed pattern when the predetermined fixed pattern is displayed in the display area for 1440 hours and then the entire screen is displayed uniformly. went.
- the process suitability is that the liquid crystal is dropped 40 pL at a time by using a constant volume metering pump 100000 times in the ODF process, and the following “0 to 200 times, 201 to 400 times, 401 to 600 times, ..., 99801 to 100,000 times ”, the change in the amount of liquid crystal dropped 200 times was evaluated in the following four stages.
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Abstract
Description
で表される化合物を少なくとも1種以上含有し、25℃における誘電率異方性が0より大きく5以下である液晶組成物により、上記課題を解決する。 (In the general formula (i), R i1 and R i2 each independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or an alkyl group having 1 to 10 carbon atoms. An alkoxy group, and at least one of R i1 and R i2 is an alkenyl group.)
The above problem is solved by a liquid crystal composition containing at least one compound represented by the formula (1) and having a dielectric anisotropy at 25 ° C. of greater than 0 and 5 or less.
で表される
本発明に係る「炭素原子数1~10個のアルキル基」の例としては、メチル基、エチル基、プロピル基、ブチル基、イソプロピル基、イソブチル基、t-ブチル基、3-ペンチル基、イソペンチル基、ネオペンチル基、ペンチル基、ヘキシル基、ヘプチル基、オクチル基、ノニル基、デシル基などが挙げられる。なお、本明細書中において、アルキル基の例は共通であり、各々のアルキル基の炭素原子数の数によって適宜上記例示から選択される。また、本発明に係る炭素原子数1~10のアルキル基は、直鎖状又は分岐状が好ましく、直鎖状がより好ましい。 (In the above formulas (i) to (iv), * represents a binding site to the ring structure.)
Examples of the “alkyl group having 1 to 10 carbon atoms” according to the present invention include methyl group, ethyl group, propyl group, butyl group, isopropyl group, isobutyl group, t-butyl group, 3- Examples include a pentyl group, an isopentyl group, a neopentyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, and a decyl group. In the present specification, examples of alkyl groups are common and are appropriately selected from the above examples depending on the number of carbon atoms of each alkyl group. Further, the alkyl group having 1 to 10 carbon atoms according to the present invention is preferably linear or branched, and more preferably linear.
R2は、炭素原子数1~10個のアルキル基、炭素原子数2~10個のアルケニル基、炭素原子数1~10個のアルコキシ基、水素原子、フッ素原子、シアノ基、-CF3または-OCF3を表し、
環A、環Bは、それぞれ独立して、
(a) 1,4-シクロヘキシレン基(この基中に存在する1個の-CH2-又は隣接していない少なくとも2個の-CH2-は-O-に置き換えられてもよい)、及び、
(b) 1,4-フェニレン基(この基中に存在する1個の-CH=又は隣接していない少なくとも2個の-CH=は-N=に置き換えられてもよい)、
からなる群より選ばれる基を表し、上記の基(a)と基(b)は、それぞれ独立して、シアノ基、フッ素原子又は塩素原子で置換されていても良く、
nは0または1を表す。)で表される化合物を少なくとも1種以上含むことが好ましい。 (In the general formula (M-1), R 1 represents an alkenyl group having 1 to 10 carbon atoms,
R 2 represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a hydrogen atom, a fluorine atom, a cyano group, —CF 3 or Represents OCF 3 ,
Ring A and Ring B are each independently
(A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and ,
(B) a 1,4-phenylene group (one —CH═ present in this group or at least two non-adjacent —CH═ may be replaced by —N═),
Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atom or a chlorine atom,
n represents 0 or 1. It is preferable that at least one compound represented by
本発明の液晶組成物において、一般式(M-1-1)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率、プロセス適合性、滴下痕、焼き付き、高速応答性、誘電率異方性などの求められる性能に応じて適宜調整する必要がある。 (In the general formula (M-1-1), R 1 represents an alkenyl group having 2 to 5 carbon atoms, and R 24 represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms. Represents.)
In the liquid crystal composition of the present invention, the content of the compound represented by the general formula (M-1-1) is low temperature solubility, transition temperature, electrical reliability, birefringence, process suitability, It is necessary to appropriately adjust according to required performance such as dripping marks, image sticking, high-speed response, and dielectric anisotropy.
OLは0、1、2又は3を表し、
BL1、BL2及びBL3は、それぞれ独立して、
(a) 1,4-シクロヘキシレン基(この基中に存在する1個の-CH2-又は隣接していない少なくとも2個の-CH2-は-O-に置き換えられてもよい)、及び、
(b) 1,4-フェニレン基(この基中に存在する1個の-CH=又は隣接していない少なくとも2個の-CH=は-N=に置き換えられてもよい)、
からなる群より選ばれる基を表し、上記の基(a)と基(b)は、それぞれ独立して、シアノ基、フッ素原子又は塩素原子で置換されていても良く、
LL1及びLL2は、それぞれ独立して、単結合、-CH2CH2-、-(CH2)4-、-OCH2-、-CH2O-、-COO-、-OCO-、-OCF2-、-CF2O-、-CH=N-N=CH-、-CH=CH-、-CF=CF-又は-C≡C-を表し、
OLが2又は3であってLL2が複数存在する場合は、それらは同一であっても異なっていても良く、OLが2又は3であってBL3が複数存在する場合は、それらは同一であっても異なっていても良いが、前記一般式(i)および前記一般式(M-1)で表される化合物を除く)で表される化合物を含むことが好ましい。 (In the general formula (L), R L1 and R L2 each independently represents an alkyl group having 1 to 8 carbon atoms, and one or non-adjacent at least two —CH in the alkyl group. 2 — may be each independently substituted by —CH═CH—, —C≡C—, —O—, —CO—, —COO— or —OCO—,
OL represents 0, 1, 2 or 3;
B L1 , B L2 and B L3 are each independently
(A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and ,
(B) a 1,4-phenylene group (one —CH═ present in this group or at least two non-adjacent —CH═ may be replaced by —N═),
Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atom or a chlorine atom,
L L1 and L L2 each independently represent a single bond, —CH 2 CH 2 —, — (CH 2 ) 4 —, —OCH 2 —, —CH 2 O—, —COO—, —OCO—, — OCF 2 —, —CF 2 O—, —CH═N—N═CH—, —CH═CH—, —CF═CF— or —C≡C—
When OL is 2 or 3 and a plurality of L L2 are present, they may be the same or different, and when OL is 2 or 3 and a plurality of B L3 is present, they are the same However, it is preferable to include a compound represented by the general formula (i) and the compound represented by the general formula (M-1).
A11およびA12はそれぞれ独立して、1,4-シクロヘキシレン基、1,4-フェニレン基、2-フルオロ-1,4-フェニレン基または3-フルオロ-1,4-フェニレン基を表す。)
前記一般式(I)で表される化合物群において組み合わせることができる化合物の種類は特に制限は無いが、低温での溶解性、粘性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて適宜組み合わせて使用する。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。また、本発明の別の実施形態では3種類である。さらに、本発明の別の実施形態では4種類である。さらに、本発明の別の実施形態では5種類である。さらに、本発明の別の実施形態では6種類以上である。 (In the general formula (I), R 11 and R 12 each independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms. One or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, and the methylene group in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group May be substituted with an oxygen atom as long as the oxygen atoms are not continuously bonded, and may be substituted with a carbonyl group unless the carbonyl group is continuously bonded;
A 11 and A 12 each independently represents a 1,4-cyclohexylene group, a 1,4-phenylene group, a 2-fluoro-1,4-phenylene group or a 3-fluoro-1,4-phenylene group. )
There are no particular restrictions on the types of compounds that can be combined in the compound group represented by the general formula (I). However, the solubility at low temperatures, viscosity, transition temperature, electrical reliability, birefringence, and the like are required. It is used in combination as appropriate according to the performance to be achieved. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types. Furthermore, in another embodiment of this invention, they are four types. Furthermore, in another embodiment of this invention, they are five types. Furthermore, in another embodiment of this invention, they are six or more types.
本発明の液晶組成物において、一般式(I-1)で表される化合物として、1~10種類、1~9種類、1~8種類、1~7種類、1~6種類、2~9種類、2~8種類、2~6種類、3~9種類、3~7種類、3~6種類または4~6種類混合して含有していることが好ましい。 (In the general formula (I-1), R 11 and R 12 have the same meaning as in the general formula (I).)
In the liquid crystal composition of the present invention, the compound represented by the general formula (I-1) is 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 2 to 9 It is preferable to contain 2 to 8 types, 2 to 6 types, 3 to 9 types, 3 to 7 types, 3 to 6 types, or 4 to 6 types mixed.
本発明に係る液晶組成物において、粘度を低く保ち、応答速度が速い液晶組成物を提供することができる観点から、一般式(I-1-1)で表される化合物群を含むことが特に好ましい。 (In the above general formula (I-1-1), R 12 represents the same meaning as in general formula (I), and R a1 is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms)
The liquid crystal composition according to the present invention particularly includes the compound group represented by the general formula (I-1-1) from the viewpoint of maintaining a low viscosity and providing a liquid crystal composition having a high response speed. preferable.
前記一般式(I-1-2)として使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。また、本発明の別の実施形態では3種類である。 (In the above general formula (I-1-2), R 12 has the same meaning as in general formula (I).)
The number of types of compounds used as the general formula (I-1-2) is, for example, one type as an embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて組み合わせる。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。また、本発明の別の実施形態では3種類である。 (In the general formula (I-2), R 13 and R 14 each independently represents an alkyl group having 1 to 5 carbon atoms.)
Although there is no restriction | limiting in particular in the kind of compound which can be combined, It combines according to performance requested | required, such as solubility at low temperature, transition temperature, electrical reliability, birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて組み合わせる。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。また、本発明の別の実施形態では3種類である。 (In the above general formula (I-3), R 13 represents the same meaning as in general formula (I-2).)
Although there is no restriction | limiting in particular in the kind of compound which can be combined, It combines according to performance requested | required, such as solubility at low temperature, transition temperature, electrical reliability, birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. In another embodiment of the present invention, there are three types.
含有量の好ましい範囲は、下記の表に示すとおりである。 In the liquid crystal composition of the present invention, the content of the compound represented by the general formula (I-3) includes solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, dropping trace Therefore, it is necessary to adjust appropriately according to required performance such as image sticking and dielectric anisotropy.
The preferable range of the content is as shown in the following table.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて組み合わせる。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。 (In the above general formula (I-4), R 11 and R 12 have the same meaning as in general formula (L).)
Although there is no restriction | limiting in particular in the kind of compound which can be combined, It combines according to performance requested | required, such as solubility at low temperature, transition temperature, electrical reliability, birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて組み合わせる。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。 (In the above general formula (I-5), R 11 and R 12 have the same meaning as in general formula (I).)
Although there is no restriction | limiting in particular in the kind of compound which can be combined, It combines according to performance requested | required, such as solubility at low temperature, transition temperature, electrical reliability, birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types.
含有量の好ましい範囲は、下記の表に示すとおりである。 In the liquid crystal composition of the present invention, the content of the compound represented by the general formula (I-5) is low temperature solubility, transition temperature, electrical reliability, birefringence index, process suitability, dripping trace. Therefore, it is necessary to adjust appropriately according to required performance such as image sticking and dielectric anisotropy.
The preferable range of the content is as shown in the following table.
前記一般式(I-6)で表される化合物の含有量は、本発明の液晶組成物の総質量に対して2質量%以上30質量%以下であることが好ましく、4質量%以上30質量%以下であることが好ましく、5質量%以上30質量%以下であることが好ましく、6質量%以上30質量%以下であることが好ましく、9質量%以上30質量%以下であることが好ましく、12質量%以上30質量%以下であることが好ましく、14質量%以上30質量%以下であることが好ましく、16質量%以上30質量%以下であることが好ましく、18質量%以上25質量%以下であることが好ましく、20質量%以上24質量%以下であることが好ましく、22質量%以上23質量%以下であることが好ましい。さらに、一般式(I-6)で表される化合物は、式(7.1)で表される化合物であることが好ましい。 (In the above general formula (I-6), R 11 and R 12 have the same meaning as in general formula (I).)
The content of the compound represented by the general formula (I-6) is preferably 2% by mass or more and 30% by mass or less with respect to the total mass of the liquid crystal composition of the present invention, and is 4% by mass or more and 30% by mass. % Or less, preferably 5% by mass or more and 30% by mass or less, preferably 6% by mass or more and 30% by mass or less, and preferably 9% by mass or more and 30% by mass or less, It is preferably 12% by mass to 30% by mass, preferably 14% by mass to 30% by mass, more preferably 16% by mass to 30% by mass, and 18% by mass to 25% by mass. It is preferable that it is 20 mass% or more and 24 mass% or less, and it is preferable that it is 22 mass% or more and 23 mass% or less. Furthermore, the compound represented by the general formula (I-6) is preferably a compound represented by the formula (7.1).
本発明の液晶組成物の総質量に対する前記一般式(I-7)で表される化合物の含有量は、1質量%以上20質量%以下であることが好ましく、1質量%以上15質量%以下であることが好ましく、1質量%以上10質量%以下であることが好ましく、1質量%以上5質量%以下であることが好ましい。 (Wherein R 11 and R 12 represent the same meaning as in general formula (I).)
The content of the compound represented by the general formula (I-7) with respect to the total mass of the liquid crystal composition of the present invention is preferably 1% by mass to 20% by mass, and preferably 1% by mass to 15% by mass. It is preferable that it is 1 mass% or more and 10 mass% or less, and it is preferable that it is 1 mass% or more and 5 mass% or less.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて、1種類から3種類組み合わせることが好ましい。また、前記一般式(I-8)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率、プロセス適合性、滴下痕、焼き付き、誘電率異方性などの求められる性能に応じて、本発明の液晶組成物の総質量に対して1~30質量%であることが好ましく、1~25質量%であることが好ましく、1~20質量%であることが好ましく、1~18質量%であることが好ましく、3~18質量%であることが好ましく、4~9質量%であることが好ましく、4~6質量%であることが好ましい。 (Wherein R 16 and R 17 each independently represents an alkenyl group having 2 to 5 carbon atoms)
Although there is no restriction | limiting in particular in the kind of compound which can be combined, According to performance requested | required, such as solubility at low temperature, transition temperature, electrical reliability, birefringence, it is preferable to combine 1 type to 3 types. . The content of the compound represented by the general formula (I-8) is the solubility at low temperature, transition temperature, electrical reliability, birefringence, process suitability, drop mark, image sticking, dielectric constant. Depending on the required performance such as anisotropy, it is preferably 1 to 30% by mass, preferably 1 to 25% by mass, and preferably 1 to 20% by mass with respect to the total mass of the liquid crystal composition of the present invention. %, Preferably 1 to 18% by mass, preferably 3 to 18% by mass, preferably 4 to 9% by mass, and preferably 4 to 6% by mass. .
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて組み合わせる。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。また、本発明のさらに別の実施形態では3種類である。さらに、本発明の別の実施形態では4種類以上である。 (In the general formula (II), R 21 and R 22 each independently represents an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms. It represents, a 2 represents a 1,4-cyclohexylene group or 1,4-phenylene group, Q 2 is a single bond, -COO -, - CH 2 -CH 2 - or an -CF 2 O-).
Although there is no restriction | limiting in particular in the kind of compound which can be combined, It combines according to performance requested | required, such as solubility at low temperature, transition temperature, electrical reliability, birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Moreover, in another embodiment of this invention, they are three types. Furthermore, in another embodiment of this invention, they are four or more types.
一般式(II-1)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて調整することが好ましい。
含有量の好ましい範囲は、下記の表に示すとおりである。 (In the general formula (II-1), R 21 and R 22 have the same meaning as in general formula (II).)
The content of the compound represented by the general formula (II-1) is preferably adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, and birefringence.
The preferable range of the content is as shown in the following table.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて組み合わせる。 (In the above general formula (II-2), R 23 represents an alkenyl group having 2 to 5 carbon atoms, and R 24 represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms. .)
Although there is no restriction | limiting in particular in the kind of compound which can be combined, It combines according to performance requested | required, such as solubility at low temperature, transition temperature, electrical reliability, birefringence.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて、これらの化合物の中から1種~3種類含有することが好ましい。 (In the general formula (II-3), R 25 represents an alkyl group having 1 to 5 carbon atoms, and R 24 represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms. .)
There are no particular restrictions on the types of compounds that can be combined, but depending on the required properties such as solubility at low temperatures, transition temperatures, electrical reliability, and birefringence, one of these compounds can be used. It is preferable to contain three types.
前記一般式(II-3-1)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて調整することが好ましく、1質量%以上24質量%以下が好ましく、4質量%以上18質量%以下であることが好ましく、6質量%以上14質量%以下であることが好ましい。 (In the general formula (II-3-1), R 25 represents an alkyl group having 1 to 5 carbon atoms, and R 26 represents an alkoxy group having 1 to 4 carbon atoms.)
The content of the compound represented by the general formula (II-3-1) can be adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, and birefringence. It is preferably 1% by mass or more and 24% by mass or less, preferably 4% by mass or more and 18% by mass or less, and more preferably 6% by mass or more and 14% by mass or less.
これらの化合物のうち1種類だけを含有していても2種類以上含有していても良いが、求められる性能に応じて適宜組み合わせることが好ましい。組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて、これらの化合物の中から1~2種類を含有することが好ましく、1~3種類を含有することがより好ましい。 (In the general formula (II-4), R 21 and R 22 are each independently an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms. Represents.)
Of these compounds, only one kind or two or more kinds may be contained, but it is preferable to combine them appropriately according to the required performance. There are no particular restrictions on the types of compounds that can be combined, but depending on the required performance such as solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc., 1 to 2 of these compounds It is preferable to include types, and it is more preferable to include one to three types.
本発明に係る一般式(II-5)で表される化合物において、X21およびX22のいずれか一方がフッ素原子であることが好ましく、X22はフッ素原子であり、かつX21は水素原子であることがより好ましい。 (In the general formula (II-5), R 25 represents an alkyl group or an alkoxy group of 1 to 4 carbon atoms alkenyl or carbon atom number of 1 to 5
In the compound represented by the general formula (II-5) according to the present invention, it is preferable that any one of X 21 and X 22 is a fluorine atom, X 22 is a fluorine atom, and X 21 is a hydrogen atom. It is more preferable that
前記一般式(III)で表される化合物の含有量は、求められる溶解性や複屈折率などを考慮して、本発明の液晶組成物の総質量に対して1質量%以上25質量%以下含有することが好ましく、2質量%以上20質量%以下含有することが好ましく、2質量%以上15質量%以下含有することが好ましく、2質量%以上10質量%以下含有することが好ましく、4質量%以上6質量%以下含有することが好ましい。 (In the general formula (III), R 31 and R 32 each independently represents an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms. To express.)
The content of the compound represented by the general formula (III) is 1% by mass or more and 25% by mass or less based on the total mass of the liquid crystal composition of the present invention in consideration of required solubility and birefringence. It is preferable to contain 2 to 20% by weight, preferably 2 to 15% by weight, preferably 2 to 10% by weight, preferably 4% by weight. % To 6% by mass is preferable.
前記一般式(III-1)で表される化合物は、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じてその含有量を調整することが好ましい。本発明の液晶組成物の総質量に対して、4質量%以上23質量%以下が好ましく、6質量%以上18質量%以下であることが好ましく、10質量%以上13質量%以下であることが好ましい。 (In the above general formula (III-1), R 33 represents an alkenyl group having 2 to 5 carbon atoms. R 32 each independently represents an alkyl group having 1 to 5 carbon atoms or an alkyl group having 1 to 4 carbon atoms. Represents an alkoxy group.)
The content of the compound represented by the general formula (III-1) is preferably adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, and birefringence. . 4 mass% or more and 23 mass% or less are preferable with respect to the total mass of the liquid-crystal composition of this invention, 6 mass% or more and 18 mass% or less are preferable, and it is 10 mass% or more and 13 mass% or less. preferable.
前記一般式(III-2)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて調整することが好ましく、本発明の液晶組成物の総質量に対して、4質量%以上23質量%以下が好ましく、6質量%以上18質量%以下であることが好ましく、10質量%以上13質量%以下であることが好ましい。 (In the general formula (III-2), R 31 has the same meaning as in general formula (III).)
The content of the compound represented by the general formula (III-2) is preferably adjusted according to required performance such as solubility at low temperature, transition temperature, electrical reliability, birefringence, 4 mass% or more and 23 mass% or less are preferable with respect to the total mass of the liquid-crystal composition of this invention, 6 mass% or more and 18 mass% or less are preferable, and it is 10 mass% or more and 13 mass% or less. preferable.
当該一般式(IV)で表される化合物の組み合わせ可能な種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて適宜組み合わせる。後述の式(18.1)から式(18.9)で表される化合物等の一般式(IV)の構造を備えた化合物を液晶組成物に添加すると、液晶組成物のΔnや他の液晶組成物を構成する成分との溶解性が向上する。
使用する化合物の種類は、例えば本発明の一つの実施形態としては1~6種類である。 (In the general formula (IV), R 41 and R 42 each independently represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, and X 41 and X 42 each independently represent Represents a hydrogen atom or a fluorine atom.)
There are no particular limitations on the types of compounds that can be combined with the compound represented by the general formula (IV). However, depending on the required performance such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence, as appropriate. combine. When a compound having a structure of the general formula (IV) such as a compound represented by the following formulas (18.1) to (18.9) is added to the liquid crystal composition, Δn of the liquid crystal composition or other liquid crystal The solubility with the component which comprises a composition improves.
The number of compounds used is, for example, 1 to 6 in one embodiment of the present invention.
一般式(IV-1)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率、プロセス適合性、滴下痕、焼き付き、誘電率異方性などの求められる性能に応じて適宜調整する必要がある。 (In the general formula (IV), R 43 and R 44 each independently represents an alkyl group having 1 to 5 carbon atoms.)
The content of the compound represented by the general formula (IV-1) is solubility at low temperature, transition temperature, electrical reliability, birefringence, process compatibility, dripping marks, image sticking, dielectric anisotropy It is necessary to adjust appropriately according to the required performance.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて適宜組み合わされる。使用する化合物の種類は、例えば本発明の一つの実施形態において1種類である。あるいは本発明の別の実施形態では2種類である。更に、本発明の別の実施形態では3種類である。更に、本発明の別の実施形態では4種類である。 (In the general formula (V), R 51 and R 52 each independently represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms. A 51 and A 52 each independently represents a 1,4-cyclohexylene group or a 1,4-phenylene group, Q 5 represents a single bond or —COO—, and X 51 and X 52 each independently represent Represents a fluorine atom or a hydrogen atom.)
There are no particular limitations on the types of compounds that can be combined, but they are appropriately combined according to required performance such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. The kind of compound to be used is, for example, one kind in one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of this invention, they are four types.
さらに、前記一般式(V-1)で表される化合物は、一般式(V-1-1)で表される化合物であることが好ましい。 (In the general formula (V-1), R 51 and R 52 , X 51 and X 52 represent the same meaning as in the general formula (V)).
Further, the compound represented by the general formula (V-1) is preferably a compound represented by the general formula (V-1-1).
前記一般式(V-1-1)で表される化合物を、本発明の液晶組成物の総質量に対して1質量%以上15質量%以下含有することが好ましく、1質量%以上10質量%以下含有することが更に好ましく、3質量%以上10質量%以下含有することが好ましく、3質量%以上7質量%以下含有することが好ましく、3質量%以上5質量%以下含有することが好ましく、3質量%以上4質量%以下含有することが好ましい。 (In the general formula (V-1-1), R 51 and R 52 represent the same meaning as in the general formula (V).)
The compound represented by the general formula (V-1-1) is preferably contained in an amount of 1% by mass or more and 15% by mass or less based on the total mass of the liquid crystal composition of the present invention. It is further preferable to contain 3 to 10% by weight, preferably 3 to 7% by weight, preferably 3 to 5% by weight, It is preferable to contain 3 mass% or more and 4 mass% or less.
前記一般式(V-1-2)で表される化合物を、本発明の液晶組成物の総質量に対して1質量%以上15質量%以下含有することが好ましく、1質量%以上10質量%以下含有することが好ましく、1質量%以上7質量%以下含有することが好ましく、1質量%以上5質量%以下含有することが好ましい。 (In the general formula (V-1-2), R 51 and R 52 represent the same meaning as in the general formula (V).)
The compound represented by the general formula (V-1-2) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention. The content is preferably 1% by mass or more and 7% by mass or less, and more preferably 1% by mass or more and 5% by mass or less.
前記一般式(V-1-3)で表される化合物を、本発明の液晶組成物の総質量に対して1質量%以上15質量%以下含有することが好ましく、2質量%以上15質量%以下含有することが好ましく、3質量%以上10質量%以下含有することが好ましく、4質量%以上8質量%以下含有することが好ましい。 (In the general formula (V-1-3), R 51 and R 52 have the same meaning as in the general formula (V).)
The compound represented by the general formula (V-1-3) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention, and preferably 2% by mass to 15% by mass. The content is preferably 3% by mass or more and 10% by mass or less, and more preferably 4% by mass or more and 8% by mass or less.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて適宜組み合わせされる。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類以上である。 (In the general formula (V-2), R 51 and R 52 , X 51 and X 52 represent the same meaning as in the general formula (V).)
There are no particular limitations on the types of compounds that can be combined, but they are appropriately combined depending on required performance such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, it is two or more types.
さらに、前記一般式(V-2-1)で表される化合物は、式(23.1)から式(23.4)で表される化合物であることが好ましく、式(23.1)または/および式(23.2)で表される化合物であることが好ましい。 (In the general formula (V-2), R 51 and R 52 represent the same meaning as in the general formula (V).)
Further, the compound represented by the general formula (V-2-1) is preferably a compound represented by the formula (23.1) to the formula (23.4), and the formula (23.1) or / And a compound represented by the formula (23.2) is preferable.
さらに、前記一般式(V-2-2)で表される化合物は、式(24.1)から式(24.4)で表される化合物であることが好ましく、式(24.1)または/および式(24.2)で表される化合物であることが好ましい。 (In the general formula (V-2-2), R 51 and R 52 represent the same meaning as in the general formula (V).)
Further, the compound represented by the general formula (V-2-2) is preferably a compound represented by the formula (24.1) to the formula (24.4), and the formula (24.1) or / And a compound represented by the formula (24.2) is preferable.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの求められる性能に応じて適宜組み合わされる。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。更に、本発明の別の実施形態では3種類以上である。 (In the general formula (V-3), R 51 and R 52 have the same meaning as in general formula (V).)
There are no particular limitations on the types of compounds that can be combined, but they are appropriately combined according to required performance such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of this invention, they are three or more types.
前記一般式(V-4)で表される化合物を、本発明の液晶組成物の総質量に対して1質量%以上15質量%以下含有することが好ましく、2質量%以上15質量%以下含有することが好ましく、3質量%以上10質量%以下含有することが好ましく、4質量%以上8質量%以下含有することが好ましい。 (In the general formula (V-4), R 51 and R 52 each independently represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkyl group having 1 to 4 carbon atoms. Represents an alkoxy group.)
The compound represented by the general formula (V-4) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention, and preferably 2% by mass or more and 15% by mass or less. It is preferable to contain 3 mass% or more and 10 mass% or less, and it is preferable to contain 4 mass% or more and 8 mass% or less.
本発明の液晶組成物の総質量に対して前記一般式(V’-5)で表される化合物を、1質量%以上15質量%以下含有することが好ましく、2質量%以上15質量%以下含有することが好ましく、2質量%以上10質量%以下含有することが好ましく、5質量%以上10質量%以下含有することが好ましい。 (In the above general formula (V′-5), R 51 and R 52 each independently represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or 1 to 4 carbon atoms. Represents an alkoxy group of
The compound represented by the general formula (V′-5) is preferably contained in an amount of 1% by mass to 15% by mass with respect to the total mass of the liquid crystal composition of the present invention, and preferably 2% by mass to 15% by mass. It is preferable to contain, it is preferable to contain 2 to 10 mass%, and it is preferable to contain 5 to 10 mass%.
前記一般式(VI)で表される化合物は、具体的には次に挙げる化合物が好適に使用できる。 (In the above general formulas (VI) and (VII), R 61 R 62 , R 71 and R 72 are each independently a linear alkyl group having 1 to 10 carbon atoms and a linear alkoxy group having 1 to 10 carbon atoms. Represents a group or a straight-chain alkenyl group having 2 to 10 carbon atoms.)
As the compound represented by the general formula (VI), specifically, the following compounds can be preferably used.
The general formula (M) according to the present invention is
PMは、0、1、2、3又は4を表し、
CM1及びCM2はそれぞれ独立して、
(d) 1,4-シクロヘキシレン基(この基中に存在する1個の-CH2-又は隣接していない2個以上の-CH2-は-O-又は-S-に置き換えられてもよい。)及び
(e) 1,4-フェニレン基(この基中に存在する1個の-CH=又は隣接していない2個以上の-CH=は-N=に置き換えられてもよい。)
からなる群より選ばれる基を表し、上記の基(d)、基(e)はそれぞれ独立してシアノ基、フッ素原子又は塩素原子で置換されていても良く、
KM1及びKM2はそれぞれ独立して単結合、-CH2CH2-、-(CH2)4-、-OCH2-、-CH2O-、-OCF2-、-CF2O-、-COO-、-OCO-又は-C≡C-を表し、
PMが2、3又は4であってKM1が複数存在する場合は、それらは同一であっても異なっていても良く、PMが2、3又は4であってCM2が複数存在する場合は、それらは同一であっても異なっていても良く、
XM1及びXM3はそれぞれ独立して水素原子、塩素原子又はフッ素原子を表し、
XM2は、水素原子、フッ素原子、塩素原子、シアノ基、トリフルオロメチル基、フルオロメトキシ基、ジフルオロメトキシ基、トリフルオロメトキシ基又は2,2,2-トリフルオロエチル基を表す。ただし、一般式(L)で表される化合物を除く。)である。 (In the general formula (M), R M1 represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms. Represents an oxy group, and one or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, the alkyl group, alkenyl group, alkoxy group or alkenyloxy group And one or more non-adjacent two or more —CH 2 — are each independently replaced by —CH═CH—, —C≡C—, —O—, —CO—, —COO— or —OCO—. May have been
PM represents 0, 1, 2, 3 or 4;
C M1 and C M2 are each independently
(D) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or nonadjacent two or more -CH 2 - may be replaced by -O- or -S- And (e) a 1,4-phenylene group (one —CH═ present in the group or two or more non-adjacent —CH═ may be replaced by —N═).
Represents a group selected from the group consisting of the above-mentioned groups (d) and (e) each independently substituted with a cyano group, a fluorine atom or a chlorine atom,
K M1 and K M2 are each independently a single bond, —CH 2 CH 2 —, — (CH 2 ) 4 —, —OCH 2 —, —CH 2 O—, —OCF 2 —, —CF 2 O—, Represents —COO—, —OCO— or —C≡C—,
When PM is 2, 3 or 4 and there are a plurality of K M1 , they may be the same or different, and when PM is 2, 3 or 4 and there are a plurality of C M2 They may be the same or different,
X M1 and X M3 each independently represent a hydrogen atom, a chlorine atom or a fluorine atom,
X M2 represents a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, a trifluoromethyl group, a fluoromethoxy group, a difluoromethoxy group, a trifluoromethoxy group, or a 2,2,2-trifluoroethyl group. However, the compound represented by the general formula (L) is excluded. ).
A2はそれぞれ独立して、1,4-シクロヘキシレンシクロヘキシレン基、1,4-フェニレン基、テトラヒドロピラン-2,5-ジイル基、ジオキサン-2,5-ジイル基又はピリミジン-2,5-ジイル基を表すが、A1が1,4-フェニレン基を表す場合、該1,4-フェニレン基中の1つ以上の水素原子はフッ素原子に置換されていてもよく、
Z2はそれぞれ独立して単結合、-OCH2-、-OCF2-、-CH2O-又は-CF2O-を表し、
Y1及びY2はそれぞれ独立して、フッ素原子又は水素原子を表し、X1はフッ素原子、-CN基又は-OCF3基を表し、
m1は、1、2、3又は4を表す。)
で表される化合物であることが好ましい。また、本発明に係る一般式(B)で表される化合物において、m1が2または3であることが好ましい。m1が2であるとより低い駆動電圧という特性がある。また、m1が3であるとより高い転移温度という特性がある。 (In the above general formula (B), R 3 represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms. Represents an oxy group, and one or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, the alkyl group, alkenyl group, alkoxy group or alkenyloxy group The methylene group therein may be substituted with an oxygen atom as long as the oxygen atoms are not continuously bonded, and may be substituted with a carbonyl group unless the carbonyl group is bonded continuously,
A 2 is each independently 1,4-cyclohexylenecyclohexylene group, 1,4-phenylene group, tetrahydropyran-2,5-diyl group, dioxane-2,5-diyl group or pyrimidine-2,5- Represents a diyl group, and when A 1 represents a 1,4-phenylene group, one or more hydrogen atoms in the 1,4-phenylene group may be substituted with fluorine atoms,
Each Z 2 independently represents a single bond, —OCH 2 —, —OCF 2 —, —CH 2 O— or —CF 2 O—;
Y 1 and Y 2 each independently represent a fluorine atom or a hydrogen atom, X 1 represents a fluorine atom, a —CN group or a —OCF 3 group,
m 1 represents 1 , 2, 3 or 4. )
It is preferable that it is a compound represented by these. In the compound represented by formula (B) according to the present invention, m 1 is preferably 2 or 3. When m 1 is 2, there is a characteristic of a lower driving voltage. Further, when m 1 is 3, there is a characteristic of a higher transition temperature.
前記一般式(X)で表される化合物において組み合わせることのできる化合物は特に制限されないが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して適宜組み合わせる。例えば、本発明の一つの実施形態では1種である。また、本発明の別の実施形態では2種類である。更に別の実施形態では3種類である。更にまた別の実施形態では4種類である。更にまた別の実施形態では5種類以上である。 However, the hydrogen atom on the 1,4-phenylene group may be substituted with a fluorine atom. )
The compounds that can be combined in the compound represented by the general formula (X) are not particularly limited, but are appropriately combined in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, and the like. For example, in one embodiment of the present invention, there is one. In another embodiment of the present invention, there are two types. In yet another embodiment, there are three types. In still another embodiment, there are four types. In still another embodiment, there are five or more types.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して実施形態ごとに適宜組み合わせる。例えば、本発明の一つの実施形態では1種である。また、本発明の別の実施形態では2種類である。更に別の実施形態では3種類である。更にまた別の実施形態では4種類である。更にまた別の実施形態では5種類以上である。 (In the general formula (X-1), X 101 to X 103 and R 10 have the same meaning as in the general formula (X).)
Although there is no restriction | limiting in particular in the compound which can be combined, It combines suitably for every embodiment in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc. For example, in one embodiment of the present invention, there is one. In another embodiment of the present invention, there are two types. In yet another embodiment, there are three types. In still another embodiment, there are four types. In still another embodiment, there are five or more types.
前記一般式(X-1-1)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの特性を考慮して適宜調整される。 (In the general formula (X-1-1), R 10 has the same meaning as in general formula (X).)
The content of the compound represented by the general formula (X-1-1) is appropriately adjusted in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence.
前記一般式(X-1-2)で表される化合物の含有量は、本発明の液晶組成物の総量に対して1質量%以上であることが好ましく、2質量%以上がより好ましく、6質量%以上がさらに好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を20質量%以下にとどめることが好ましく、16質量%以下がさらに好ましく、12質量%以下がより好ましく、10質量%以下が特に好ましい。 (In the general formula (X-1-2), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
The content of the compound represented by the general formula (X-1-2) is preferably 1% by mass or more, more preferably 2% by mass or more, based on the total amount of the liquid crystal composition of the present invention. The mass% or more is more preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably 20% by mass or less, more preferably 16% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましい。 (In the general formula (X-1-3), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more of them in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましい。 (In the general formula (X-2), X 102 to X 103 each independently represents a fluorine atom or a hydrogen atom, Y 10 represents a fluorine atom, a chlorine atom, or —OCF 3 , and R 10 represents the number of carbon atoms. Represents an alkyl group having 1 to 5, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more of them in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましく、1種から3種類以上組み合わせることがより好ましい。 (In the general formula (X-2-1), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine more than one type.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましい。一般式(X-2-2)で表される化合物の含有量は、本発明の液晶組成物の総量に対して1質量%以上であることが好ましく、2質量%以上がより好ましく、3質量%以上がさらに好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を20質量%以下にとどめることが好ましく、16質量%以下がさらに好ましく、12質量%以下がより好ましく、10質量%以下が特に好ましい。 (In the general formula (X-2-2), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more of them in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like. The content of the compound represented by the general formula (X-2-2) is preferably 1% by mass or more, more preferably 2% by mass or more, based on the total amount of the liquid crystal composition of the present invention. % Or more is more preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably 20% by mass or less, more preferably 16% by mass or less, and even more preferably 12% by mass or less. 10 mass% or less is especially preferable.
A2bはそれぞれ独立して、1,4-シクロヘキシレンシクロヘキシレン基、1,4-フェニレン基、テトラヒドロピラン-2,5-ジイル基、ジオキサン-2,5-ジイル基又はピリミジン-2,5-ジイル基を表すが、A2bが1,4-フェニレン基を表す場合、該1,4-フェニレン基中の1つ以上の水素原子はフッ素原子に置換されていてもよく、
Z2bはそれぞれ独立して単結合、-OCH2-、-OCF2-、-CH2O-、又は-CF2O-を表し、
m2bは、1、2、3又は4を表し、Y3bはそれぞれ独立してフッ素原子又は水素原子を表し、X1bはフッ素原子、-CN基又は-OCF3基を表す。)で表される化合物群の中から少なくとも1種類の化合物が選択されることが好ましく、前記m2bは2、3がより好ましい。 (In the general formula (IIb), R 3b represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkyl group having 2 to 8 carbon atoms. Represents an alkenyloxy group, and one or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, the alkyl group, alkenyl group, alkoxy group or alkenyloxy The methylene group in the group may be substituted with an oxygen atom unless oxygen atoms are continuously bonded, and may be substituted with a carbonyl group unless a carbonyl group is bonded continuously;
A 2b independently represents 1,4-cyclohexylenecyclohexylene group, 1,4-phenylene group, tetrahydropyran-2,5-diyl group, dioxane-2,5-diyl group or pyrimidine-2,5- Represents a diyl group, and when A 2b represents a 1,4-phenylene group, one or more hydrogen atoms in the 1,4-phenylene group may be substituted with fluorine atoms,
Each Z 2b independently represents a single bond, —OCH 2 —, —OCF 2 —, —CH 2 O—, or —CF 2 O—;
m 2b represents 1, 2, 3 or 4, Y 3b independently represents a fluorine atom or a hydrogen atom, and X 1b represents a fluorine atom, a —CN group or a —OCF 3 group. It is preferable that at least one compound is selected from the compound group represented by (2), and the m 2b is more preferably 2 or 3.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましい。前記一般式(X-3)で表される化合物を液晶組成物に含むと、Δεなどの誘電性を確保できるだけでなく、一般式(L)などの第一成分との相溶性も損なわれない。 (In the general formula (X-3), X 102 to X 103 each independently represents a fluorine atom or a hydrogen atom, and R 10 represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms. Represents a group or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more of them in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like. When the liquid crystal composition contains the compound represented by the general formula (X-3), not only dielectric properties such as Δε can be secured, but also compatibility with the first component such as the general formula (L) is not impaired. .
一般式(X-3-1)を満たす化合物において、組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましい。 (In the general formula (X-3-1), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
In the compound satisfying the general formula (X-3-1), there are no particular limitations on the compounds that can be combined, but in consideration of solubility at a low temperature, transition temperature, electrical reliability, birefringence, etc. It is preferable to combine two or more species.
一般式(X-3-2)を満たす化合物において、組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましい。 (In the general formula (X-3-2), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
In the compound satisfying the general formula (X-3-2), there are no particular limitations on the compounds that can be combined, but in view of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc. It is preferable to combine two or more species.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましく、1種から3種類以上組み合わせることがより好ましい。 (In the general formula (X-4), X 102 represents a fluorine atom or a hydrogen atom, R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or 1 to 4 represents an alkoxy group.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine more than one type.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましく、1種から3種類以上組み合わせることがより好ましい。 (In the general formula (X-4-1), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine more than one type.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましく、1種から3種類以上組み合わせることがより好ましい。 (In the general formula (X-5), X 102 represents a fluorine atom or a hydrogen atom, and R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or 1 to 4 represents an alkoxy group.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine more than one type.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましく、1種から3種類以上組み合わせることがより好ましい。 (In the general formula (X-5-1), R 10 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine more than one type.
本発明に係る液晶組成物において、上記一般式(X-6-1)において、組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して、例えば本発明の一つの実施形態としては1~5種類である。あるいは本発明の別の実施形態では1~4種類である。また、本発明の別の実施形態では1~3種類である。さらに、本発明の別の実施形態では1~2種類である。さらに、本発明の別の実施形態では2~5種類である。さらに、本発明の別の実施形態では2~4種類である。さらに、本発明の別の実施形態では2~3種類である。 (In the above general formulas (X-6-1) and (X-6-2), RM1, X M12 , X M13 , X M14 , X M15 , X M16 , X M17, and Y M11 are represented by the above general formula (X Same as -6).)
In the liquid crystal composition according to the present invention, the compound that can be combined in the general formula (X-6-1) is not particularly limited, but solubility at low temperature, transition temperature, electrical reliability, birefringence Considering the rate and the like, for example, one embodiment of the present invention has 1 to 5 types. Alternatively, in another embodiment of the present invention, there are 1 to 4 types. In another embodiment of the present invention, there are 1 to 3 types. Furthermore, in another embodiment of the present invention, there are one or two types. Furthermore, in another embodiment of the present invention, there are 2 to 5 types. Furthermore, in another embodiment of the present invention, there are 2 to 4 types. Furthermore, in another embodiment of the present invention, there are two to three types.
A2aはそれぞれ独立して、1,4-シクロヘキシレンシクロヘキシレン基、1,4-フェニレン基、テトラヒドロピラン-2,5-ジイル基、ジオキサン-2,5-ジイル基又はピリミジン-2,5-ジイル基を表すが、A2aが1,4-フェニレン基を表す場合、該1,4-フェニレン基中の1つ以上の水素原子はフッ素原子に置換されていてもよく、
Z2aはそれぞれ独立して単結合、-OCH2-、-OCF2-、-CH2O-、又は-CF2O-を表し、
m2aは、1、2、3又は4を表し、Y3aはそれぞれ独立してフッ素原子又は水素原子を表し、X1aはフッ素原子、-CN基又は-OCF3基を表す。)で表される化合物群の中から少なくとも1種類の化合物が選択されることが好ましく、前記一般式(IIa)で表される化合物から少なくとも2種類の化合物が選択されることがより好ましい。また、前記一般式(IIa)において、m2aが2、3又は4であることがより好ましく、m2aが2又は3であることがさらに好ましく、m2aが3であることが特に好ましい。 (In the general formula (IIa), R 3a is an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkyl group having 2 to 8 carbon atoms. Represents an alkenyloxy group, and one or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, the alkyl group, alkenyl group, alkoxy group or alkenyloxy The methylene group in the group may be substituted with an oxygen atom unless oxygen atoms are continuously bonded, and may be substituted with a carbonyl group unless a carbonyl group is bonded continuously;
A 2a is each independently 1,4-cyclohexylenecyclohexylene group, 1,4-phenylene group, tetrahydropyran-2,5-diyl group, dioxane-2,5-diyl group or pyrimidine-2,5- Represents a diyl group, and when A 2a represents a 1,4-phenylene group, one or more hydrogen atoms in the 1,4-phenylene group may be substituted with fluorine atoms,
Each Z 2a independently represents a single bond, —OCH 2 —, —OCF 2 —, —CH 2 O—, or —CF 2 O—;
m 2a represents 1, 2, 3 or 4, Y 3a independently represents a fluorine atom or a hydrogen atom, and X 1a represents a fluorine atom, a —CN group or a —OCF 3 group. It is preferable that at least one kind of compound is selected from the compound group represented by the formula (IIa), and it is more preferable that at least two kinds of compounds are selected from the compound represented by the general formula (IIa). In the general formula (IIa), m 2a is more preferably 2 , 3 or 4, more preferably m 2a is 2 or 3, and particularly preferably m 2a is 3.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から3種類以上組み合わせることが好ましい。 (In the general formula (XI), X 111 to X 117 each independently represents a fluorine atom or a hydrogen atom, at least one of X 111 to X 117 represents a fluorine atom, and R 11 represents 1 to 5 represents an alkyl group, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms, and Y 11 represents a fluorine atom or —OCF 3. )
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one to three or more in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して、実施形態ごとに適宜組み合わせる。例えば、本発明の一つの実施形態では1種類、別の実施形態では2種類、更に別の実施形態では3種類以上組み合わせる。 (In the general formula (XI-1), R 11 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
Although there is no restriction | limiting in particular in the compound which can be combined, In consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc., it combines suitably for every embodiment. For example, in one embodiment of the present invention, one type is combined, in another embodiment, two types, and in another embodiment, three or more types are combined.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から3種類以上組み合わせることが好ましく、1種から4種類以上組み合わせることがより好ましい。 (In the general formula (XII), X 121 to X 126 each independently represents a fluorine atom or a hydrogen atom, and R 12 represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms. Or an alkoxy group having 1 to 4 carbon atoms, and Y 12 represents a fluorine atom or —OCF 3. )
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one to three or more in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like. It is more preferable to combine more than one type.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましく、1種から3種類以上組み合わせることがより好ましい。 (In the general formula (XII-1), R 12 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine more than one type.
組み合わせることのできる化合物に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から2種類以上組み合わせることが好ましく、1種から3種類以上組み合わせることがより好ましい。 (In the general formula (XII-2), R 12 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular limitations on the compounds that can be combined, but it is preferable to combine one or more types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine more than one type.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの所望の性能に応じて適宜組み合わせて使用される。使用される化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。更に、本発明の別の実施形態では3種類以上である。前記一般式(VIII)で表される化合物が液晶組成物中に存在すると、高いΔnを示し、また他の4環化合物との比率調整によって転移点をコントロールしやすいという作用・効果を奏する。 (In the general formula (VIII), R 8 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms, and X 81 to X 85 are Each independently represents a hydrogen atom or a fluorine atom, and Y 8 represents a fluorine atom or —OCF 3. )
Although there is no restriction | limiting in particular in the kind of compound which can be combined, According to desired performances, such as low temperature solubility, transition temperature, electrical reliability, birefringence, it uses suitably combining. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of this invention, they are three or more types. When the compound represented by the general formula (VIII) is present in the liquid crystal composition, it exhibits high Δn, and has an effect that the transition point can be easily controlled by adjusting the ratio with other tetracyclic compounds.
さらに、一般式(VIII-1)で表される化合物は、具体的には式(26.1)から式(26.4)で表される化合物であることが好ましく、式(26.1)または式(26.2)で表される化合物が好ましく、式(26.2)で表される化合物がさらに好ましい。 (In the general formula (VIII-1), R 8 has the same meaning as in general formula (VIII).)
Further, the compound represented by the general formula (VIII-1) is specifically preferably a compound represented by the formula (26.1) to the formula (26.4), and the formula (26.1) Or the compound represented by Formula (26.2) is preferable, and the compound represented by Formula (26.2) is more preferable.
一般式(VIII-2)として組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの所望の性能に応じて適宜組み合わせて使用する。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。あるいは、本発明の更に別の実施形態では3種類以上である。 (In the above general formula (VIII-2), R 8 represents the same meaning as in general formula (VIII).)
There are no particular restrictions on the types of compounds that can be combined as the general formula (VIII-2), but they are appropriately combined according to desired performance such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. To use. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Or in another embodiment of this invention, they are three or more types.
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの所望の性能に応じて適宜組み合わせて使用する。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類以上である。 (In the general formula (IX), R 9 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms, and X 91 and X 92 are Each independently represents a hydrogen atom or a fluorine atom, Y 9 represents a fluorine atom, a chlorine atom or —OCF 3 , and U 9 represents a single bond, —COO— or —CF 2 O—.)
There are no particular restrictions on the types of compounds that can be combined, but they are used in appropriate combinations according to desired properties such as solubility at low temperatures, transition temperatures, electrical reliability, and birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, it is two or more types.
さらに、本発明に係る一般式(IX-1)で表される化合物は、一般式(IX-1-1)で表される化合物であることが好ましい。 (In the general formula (IX-1), R 9 and X 92 have the same meaning as in general formula (IX).)
Further, the compound represented by the general formula (IX-1) according to the present invention is preferably a compound represented by the general formula (IX-1-1).
組み合わせることができる化合物の種類に特に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの所望の性能に応じて適宜組み合わせて使用する。使用する化合物の種類は、例えば本発明の一つの実施形態としては1種類である。あるいは本発明の別の実施形態では2種類である。更に、本発明の別の実施形態では3種類以上である。 (In the general formula (IX-1-1), R 9 has the same meaning as in general formula (IX).)
There are no particular restrictions on the types of compounds that can be combined, but they are used in appropriate combinations according to desired properties such as solubility at low temperatures, transition temperatures, electrical reliability, and birefringence. The kind of the compound used is, for example, one kind as one embodiment of the present invention. Or in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of this invention, they are three or more types.
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から3種類を組み合わせることが好ましく、1種から4種類を組み合わせることがより好ましい。 (In the above (IX-1-2), R 9 represents the same meaning as in general formula (IX).)
Although there is no restriction | limiting in the kind of compound which can be combined, It is preferable to combine 1 type to 3 types in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc. It is more preferable to combine the four types.
さらに、本発明に係る一般式(IX-2)で表される化合物は、一般式(IX-2-1)で表される化合物であることが好ましい。 (In the general formula (IX-2), R 9 , X 91 and X 92 represent the same meaning as in the general formula (IX).)
Furthermore, the compound represented by the general formula (IX-2) according to the present invention is preferably a compound represented by the general formula (IX-2-1).
例えば、本発明の一つの実施形態では、本発明の液晶組成物の総質量に対して、前記一般式(IX-2-1)で表される化合物の含有量は、1~25質量%である。別の実施形態では前記化合物の含有量は1~20質量%である。更に別の実施形態では前記化合物の含有量は1~15質量%である。また更に別の実施形態では前記化合物の含有量は1~10質量%である。また更に別の実施形態では前記化合物の含有量は1~5質量%である。また更に別の実施形態では前記化合物の含有量は1~4質量%である。 (In the above general formula (IX-2-1), R 9 has the same meaning as in general formula (IX).)
For example, in one embodiment of the present invention, the content of the compound represented by the general formula (IX-2-1) is 1 to 25% by mass with respect to the total mass of the liquid crystal composition of the present invention. is there. In another embodiment, the content of the compound is 1-20% by mass. In still another embodiment, the content of the compound is 1% to 15% by mass. In still another embodiment, the content of the compound is 1% to 10% by mass. In still another embodiment, the content of the compound is 1% to 5% by mass. In still another embodiment, the content of the compound is 1% to 4% by mass.
前記一般式(IX-2-2)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性、複屈折率などの特性を考慮して実施形態ごとに適宜調整される。 (In the above general formula (IX-2-2), R 9 represents the same meaning as in general formula (IX).)
The content of the compound represented by the general formula (IX-2-2) is appropriately determined for each embodiment in consideration of properties such as solubility at low temperatures, transition temperature, electrical reliability, and birefringence. Adjusted.
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1~2種類を組み合わせることが好ましい。 (In the general formula (IX-2-3), R 9 represents the same meaning as in the general formula (IX).)
There are no limitations on the types of compounds that can be combined, but it is preferable to combine one or two types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like.
前記一般式(IX-2-4)で表される化合物の含有量は、低温での溶解性、転移温度、電気的な信頼性などを考慮して、本発明の液晶組成物の総質量に対して、1質量%以上25質量%以下であることが好ましく、1質量%以上20質量%以下が好ましく、1質量%以上15質量%以下が好ましく、1質量%以上12質量%以下が好ましく、5質量%以上12質量%以下が好ましく、7質量%以上12質量%以下が好ましい。 (In the above general formula (IX-2-4), R 9 represents the same meaning as in general formula (IX).)
The content of the compound represented by the general formula (IX-2-4) is based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, transition temperature, electrical reliability, and the like. On the other hand, it is preferably 1% by mass to 25% by mass, preferably 1% by mass to 20% by mass, preferably 1% by mass to 15% by mass, and preferably 1% by mass to 12% by mass, 5 mass% or more and 12 mass% or less are preferable, and 7 mass% or more and 12 mass% or less are preferable.
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して、実施形態ごとに適宜組み合わせて使用する。例えば、本発明の一つの実施形態では1種類、別の実施形態では2種類、更に別の実施形態では3種類、また更に別の実施形態では4種類以上である。 (In the general formula (IX-2-5), R 9 has the same meaning as in general formula (IX).)
Although there is no restriction | limiting in the kind of compound which can be combined, Considering solubility at low temperature, transition temperature, electrical reliability, birefringence, etc., it uses combining suitably for every embodiment. For example, one embodiment of the present invention has one type, another embodiment has two types, yet another embodiment has three types, and yet another embodiment has four or more types.
さらに、一前記般式(IX-3)で表される化合物は、一般式(IX-3-1)で表される化合物であることが好ましい。 (In the general formula (IX-3), R 9 , X 91 and X 92 represent the same meaning as in the general formula (IX).)
Further, the compound represented by the general formula (IX-3) is preferably a compound represented by the general formula (IX-3-1).
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1~2種類を組み合わせることが好ましい。 (In the general formula (IX-3-1), R 9 has the same meaning as in general formula (IX).)
There are no limitations on the types of compounds that can be combined, but it is preferable to combine one or two types in consideration of solubility at low temperatures, transition temperature, electrical reliability, birefringence, and the like.
組み合わせることができる化合物の種類に特に制限は無いが、これらの化合物の中から1種~2種類含有することが好ましく、1種~3種類含有することがより好ましく、1種~4種類含有することが更に好ましい。 (In the general formula (XIII), X 131 to X 135 each independently represents a fluorine atom or a hydrogen atom, and R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or Represents an alkoxy group having 1 to 4 carbon atoms, and Y 13 represents a fluorine atom or —OCF 3. )
There are no particular restrictions on the types of compounds that can be combined, but one to two of these compounds are preferably contained, more preferably one to three, and more preferably one to four. More preferably.
一般式(XIII-1)で表される化合物を本発明の液晶組成物の総量に対して1質量%以上含有することが好ましく、3質量%以上含有することがさらに好ましく、5質量%以上含有することがさらに好ましく、10質量%以上含有することが特に好ましい。また、最大に含有できる比率としては、25質量%以下が好ましく、20質量%以下がより好ましく、15質量%以下がさらに好ましい。 (In the general formula (XIII-1), R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
The compound represented by the general formula (XIII-1) is preferably contained in an amount of 1% by mass or more, more preferably 3% by mass or more, based on the total amount of the liquid crystal composition of the present invention, It is more preferable to contain 10% by mass or more. Moreover, as a ratio which can be contained at the maximum, 25 mass% or less is preferable, 20 mass% or less is more preferable, and 15 mass% or less is further more preferable.
組み合わせることができる化合物の種類に特に制限は無いが、これらの化合物の中から1種~2種類以上含有することが好ましい。 (In the general formula (XIII-2), R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular restrictions on the types of compounds that can be combined, but it is preferable to contain one or more of these compounds.
組み合わせることができる化合物の種類に特に制限は無いが、これらの化合物の中から1種~2種類含有することが好ましい。 (In the general formula (XIII-3), R 13 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
There are no particular restrictions on the types of compounds that can be combined, but it is preferable to contain one or two of these compounds.
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して実施形態ごとに適宜組み合わせる。例えば、本発明の一つの実施形態では1種である。さらに、本発明の別の実施形態では2種類である。あるいは、本発明のさらに別の実施形態では3種類である。また、本発明のさらに別の実施形態では4種類である。あるいは、本発明のさらに別の実施形態では5種類である。あるいは、本発明のさらに別の実施形態では6種類以上である。 (In the general formula (XIV), R 14 represents an alkyl group, an alkenyl group or an alkoxy group having 1 to 7 carbon atoms of 2 to 7 carbon atoms of 1 to 7 carbon atoms, and from X 141 X 144 each independently represents a fluorine atom or a hydrogen atom, Y 14 represents a fluorine atom, a chlorine atom or —OCF 3 , Q 14 represents a single bond, —COO— or —CF 2 O—, and m 14 represents 0 or 1)
Although there is no restriction | limiting in the kind of compound which can be combined, It combines suitably for every embodiment in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc. For example, in one embodiment of the present invention, there is one. Furthermore, in another embodiment of this invention, they are two types. Or in another embodiment of this invention, they are three types. In still another embodiment of the present invention, there are four types. Or in another embodiment of this invention, they are five types. Or in another embodiment of this invention, they are six or more types.
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して1種から3種類組み合わせることが好ましい。 (In the general formula (XIV-1), R 14 represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms, or an alkoxy group having 1 to 7 carbon atoms, and Y 14 represents fluorine. Represents an atom, a chlorine atom or —OCF 3 )
Although there is no restriction | limiting in the kind of compound which can be combined, It is preferable to combine 1 type to 3 types in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc.
前記一般式(XIV-1)で表される化合物の含有量は、本発明の液晶組成物の総量に対して2質量%以上であることが好ましく、4質量%以上がより好ましく、7質量%以上がさらに好ましく、10質量%以上がさらに好ましく、18質量%以上が特に好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を30質量%以下にとどめることが好ましく、27質量%以下がさらに好ましく、24質量%以下がより好ましく、21質量%未満が特に好ましい。 (In the general formula (XIV-1), R 14 represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms, or an alkoxy group having 1 to 7 carbon atoms.)
The content of the compound represented by the general formula (XIV-1) is preferably 2% by mass or more, more preferably 4% by mass or more, and more preferably 7% by mass with respect to the total amount of the liquid crystal composition of the present invention. The above is more preferable, 10% by mass or more is more preferable, and 18% by mass or more is particularly preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably limited to 30% by mass or less, more preferably 27% by mass or less, and more preferably 24% by mass or less. , Less than 21% by mass is particularly preferable.
一般式(XIV-1-2)で表される化合物の含有量は、本発明の液晶組成物の総量に対して1質量%以上であることが好ましく、3質量%以上がより好ましく、5質量%以上がさらに好ましく、7質量%以上が特に好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を15質量%以下にとどめることが好ましく、13質量%以下がさらに好ましく、11質量%以下がより好ましく、9質量%未満が特に好ましい。 (In the above general formula (XIV-1-2), R 14 represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms, or an alkoxy group having 1 to 7 carbon atoms.)
The content of the compound represented by the general formula (XIV-1-2) is preferably 1% by mass or more, more preferably 3% by mass or more, more preferably 5% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is more preferable, and 7 mass% or more is particularly preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably 15% by mass or less, more preferably 13% by mass or less, and even more preferably 11% by mass or less. , Less than 9% by mass is particularly preferable.
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して実施形態ごとに適宜組み合わせる。例えば、本発明の一つの実施形態では1種である。さらに、本発明の別の実施形態では2種類である。あるいは、本発明のさらに別の実施形態では3種類である。また、本発明のさらに別の実施形態では4種類である。あるいは、本発明のさらに別の実施形態では5種類以上である。 (In the general formula (XIV-2), R 14 represents an alkyl group, an alkenyl group or an alkoxy group having 1 to 4 carbon atoms of 2 to 5 carbon atoms of 1 to 5 carbon atoms, from X 141 X 144 each independently represents a fluorine atom or a hydrogen atom, and Y 14 represents a fluorine atom, a chlorine atom or —OCF 3 )
Although there is no restriction | limiting in the kind of compound which can be combined, It combines suitably for every embodiment in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc. For example, in one embodiment of the present invention, there is one. Furthermore, in another embodiment of this invention, they are two types. Or in another embodiment of this invention, they are three types. In still another embodiment of the present invention, there are four types. Or in another embodiment of this invention, they are five or more types.
一般式(XIV-2-1)で表される化合物の含有量は、本発明の液晶組成物の総量に対して1質量%以上であることが好ましく、3質量%以上がより好ましく、5質量%以上がさらに好ましく、7質量%以上が特に好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を15質量%以下にとどめることが好ましく、13質量%以下がさらに好ましく、11質量%以下がより好ましく、9質量%未満が特に好ましい。 (In the above general formula (XIV-2-1), R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
The content of the compound represented by the general formula (XIV-2-1) is preferably 1% by mass or more, more preferably 3% by mass or more, with respect to the total amount of the liquid crystal composition of the present invention. % Or more is more preferable, and 7 mass% or more is particularly preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably 15% by mass or less, more preferably 13% by mass or less, and even more preferably 11% by mass or less. , Less than 9% by mass is particularly preferable.
一般式(XIV-2-2)で表される化合物の含有量は、本発明の液晶組成物の総量に対して3質量%以上であることが好ましく、6質量%以上がより好ましく、9質量%以上がさらに好ましく、12質量%以上が特に好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を20質量%以下にとどめることが好ましく、17質量%以下がさらに好ましく、15質量%以下がより好ましく、14質量%以下が特に好ましい。 (In the above general formula (XIV-2-2), R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
The content of the compound represented by the general formula (XIV-2-2) is preferably 3% by mass or more, more preferably 6% by mass or more, and more preferably 9% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is more preferable, and 12% by mass or more is particularly preferable. In consideration of solubility at low temperature, transition temperature, electrical reliability, etc., the maximum ratio is preferably 20% by mass or less, more preferably 17% by mass or less, and even more preferably 15% by mass or less. 14 mass% or less is particularly preferable.
一般式(XIV-2-3)で表される化合物の含有量は、本発明の液晶組成物の総量に対して5質量%以上であることが好ましく、9質量%以上がより好ましく、12質量%以上が特に好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を30質量%以下にとどめることが好ましく、27質量%未満がさらに好ましく、24質量%以下がより好ましく、20質量%未満が特に好ましい。 (In the general formula (XIV-2-3), R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
The content of the compound represented by the general formula (XIV-2-3) is preferably 5% by mass or more, more preferably 9% by mass or more, and more preferably 12% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is particularly preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably limited to 30% by mass or less, more preferably less than 27% by mass, and even more preferably 24% by mass or less. , Less than 20% by mass is particularly preferable.
組み合わせることのできる化合物の種類に制限は無いが、低温での溶解性、転移温度、電気的な信頼性、複屈折率などを考慮して実施形態ごとに適宜組み合わせる。例えば、本発明の一つの実施形態では1種である。さらに、本発明の別の実施形態では2種類である。あるいは、本発明のさらに別の実施形態では3種類以上である。 (In the above general formula (XIV-2-4), R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
Although there is no restriction | limiting in the kind of compound which can be combined, It combines suitably for every embodiment in consideration of solubility at low temperature, transition temperature, electrical reliability, birefringence, etc. For example, in one embodiment of the present invention, there is one. Furthermore, in another embodiment of this invention, they are two types. Or in another embodiment of this invention, they are three or more types.
The upper limit of the content is, for example, 15% in one embodiment of the present invention, 12% in another embodiment, 11% in still another embodiment, 10% in yet another embodiment, In yet another embodiment it is 8%, and in yet another
一般式(XIV-2-5)で表される化合物の含有量は、本発明の液晶組成物の総量に対して5質量%以上であることが好ましく、10質量%以上がより好ましく、13質量%以上が特に好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を25質量%以下にとどめることが好ましく、22質量%未満がさらに好ましく、18質量%以下がより好ましく、15質量%未満が特に好ましい。 (In the above general formula (XIV-2-5), R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
The content of the compound represented by the general formula (XIV-2-5) is preferably 5% by mass or more, more preferably 10% by mass or more, and more preferably 13% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is particularly preferable. In consideration of solubility at low temperatures, transition temperature, electrical reliability, etc., the maximum ratio is preferably limited to 25% by mass or less, more preferably less than 22% by mass, and even more preferably 18% by mass or less. , Less than 15% by mass is particularly preferable.
一般式(XIV-2-6)で表される化合物の含有量は、本発明の液晶組成物の総量に対して5質量%以上であることが好ましく、10質量%以上がより好ましく、15質量%以上が特に好ましい。また、低温での溶解性、転移温度、電気的な信頼性などを考慮して、最大比率を25質量%以下にとどめることが好ましく、22質量%以下がさらに好ましく、20質量%以下がより好ましく、17質量%未満が特に好ましい。 (Wherein R 14 represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or an alkoxy group having 1 to 4 carbon atoms.)
The content of the compound represented by the general formula (XIV-2-6) is preferably 5% by mass or more, more preferably 10% by mass or more, and more preferably 15% by mass with respect to the total amount of the liquid crystal composition of the present invention. % Or more is particularly preferable. In consideration of solubility at low temperature, transition temperature, electrical reliability, etc., the maximum ratio is preferably limited to 25% by mass or less, more preferably 22% by mass or less, and even more preferably 20% by mass or less. , Less than 17% by mass is particularly preferable.
で表される化合物を少なくとも1種以上と、
一般式(M-1): (In the general formula (i), R i1 and R i2 each independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or an alkyl group having 1 to 10 carbon atoms. An alkoxy group, and at least one of R i1 and R i2 is an alkenyl group.)
At least one compound represented by:
Formula (M-1):
R2は、炭素原子数1~10個のアルキル基、炭素原子数2~10個のアルケニル基ま、炭素原子数1~10個のアルコキシ基、水素原子、フッ素原子、シアノ基、-CF3または-OCF3を表し、
環A、環Bは、それぞれ独立して、
(a) 1,4-シクロヘキシレン基(この基中に存在する1個の-CH2-又は隣接していない少なくとも2個の-CH2-は-O-に置き換えられてもよい)、及び、
(b) 1,4-フェニレン基(この基中に存在する1個の-CH=又は隣接していない少なくとも2個の-CH=は-N=に置き換えられてもよい)、
からなる群より選ばれる基を表し、上記の基(a)と基(b)は、それぞれ独立して、シアノ基、フッ素原子又は塩素原子で置換されていても良く、
nは0または1を表す。)
で表される化合物を少なくとも1種以上と、
一般式(I-1): (In the general formula (M-1), R 1 represents an alkenyl group having 2 to 10 carbon atoms,
R 2 represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a hydrogen atom, a fluorine atom, a cyano group, —CF 3 Or represents -OCF 3
Ring A and Ring B are each independently
(A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and ,
(B) a 1,4-phenylene group (one —CH═ present in this group or at least two non-adjacent —CH═ may be replaced by —N═),
Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atom or a chlorine atom,
n represents 0 or 1. )
At least one compound represented by:
Formula (I-1):
を含み、かつ25℃における誘電率異方性が0より大きく5以下である液晶組成物である。 (In the general formula (I-1), R 11 and R 12 are each independently an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, or an alkenyl having 2 to 8 carbon atoms. And one or more hydrogen atoms in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group may be substituted with a fluorine atom, in the alkyl group, alkenyl group, alkoxy group or alkenyloxy group. The methylene group may be substituted with an oxygen atom unless oxygen atoms are continuously bonded, and may be substituted with a carbonyl group unless a carbonyl group is bonded continuously. With one or more,
And a dielectric anisotropy at 25 ° C. of greater than 0 and 5 or less.
Sp201及びSp202は、それぞれ独立して、単結合、炭素原子数1~8のアルキレン基又は-O-(CH2)S-(式中、sは2~7の整数を表し、酸素原子は芳香環に結合するものとする。)を表し、
Z201は、-OCH2-、-CH2O-、-COO-、-OCO-、-CF2O-、-OCF2-、-CH2CH2-、-CF2CF2-、-CH=CH-COO-、-CH=CH-OCO-、-COO-CH=CH-、-OCO-CH=CH-、-COO-CH2CH2-、-OCO-CH2CH2-、-CH2CH2-COO-、-CH2CH2-OCO-、-COO-CH2-、-OCO-CH2-、-CH2-COO-、-CH2-OCO-、-CY1=CY2-(式中、Y1及びY2は、それぞれ独立して、フッ素原子又は水素原子を表す。)、-C≡C-、又は、単結合を表し、
M201は、トランス-1,4-シクロヘキシレン基、単結合または任意の水素原子がフッ素原子により置換されていても良い1,4-フェニレン基を表し、
上記一般式(XX)中の全ての1,4-フェニレン基は、任意の水素原子がフッ素原子により置換されていても良い。 In the general formula (XX), X 201 and X 202 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms (methyl group, ethyl group, propyl group),
Sp 201 and Sp 202 each independently represent a single bond, an alkylene group having 1 to 8 carbon atoms or —O— (CH 2 ) S — (wherein s represents an integer of 2 to 7, Represents an aromatic ring)),
Z 201 represents —OCH 2 —, —CH 2 O—, —COO—, —OCO—, —CF 2 O—, —OCF 2 —, —CH 2 CH 2 —, —CF 2 CF 2 —, —CH ═CH—COO—, —CH═CH—OCO—, —COO—CH═CH—, —OCO—CH═CH—, —COO—CH 2 CH 2 —, —OCO—CH 2 CH 2 —, —CH 2 CH 2 —COO—, —CH 2 CH 2 —OCO—, —COO—CH 2 —, —OCO—CH 2 —, —CH 2 —COO—, —CH 2 —OCO—, —CY 1 = CY 2 -(Wherein Y 1 and Y 2 each independently represents a fluorine atom or a hydrogen atom), -C≡C-, or a single bond;
M 201 represents a trans-1,4-cyclohexylene group, a single bond or a 1,4-phenylene group in which any hydrogen atom may be substituted by a fluorine atom,
In all of the 1,4-phenylene groups in the general formula (XX), any hydrogen atom may be substituted with a fluorine atom.
また、本発明に係る液晶表示素子の駆動方式(またはモードとも称する。)としては、ECB-LCD、VA-LCD、VA-IPS-LCD、FFS(フリンジ・フィールド・スイッチング)-LCD、TN(ネマチック液晶表示素子)、STN-LCD(超ねじれネマチック液晶表示素子)、OCB-LCD及びIPS-LCD(インプレーンスイッチング液晶表示素子)に有用であるが、IPSモードまたはFFSモードの液晶表示素子が特に好ましい。 The liquid crystal display element according to the present invention is useful for an AM-LCD (active matrix liquid crystal display element) and can be used for a transmissive or reflective liquid crystal display element.
Further, as a driving method (or mode) of the liquid crystal display element according to the present invention, ECB-LCD, VA-LCD, VA-IPS-LCD, FFS (fringe field switching) -LCD, TN (nematic) It is useful for liquid crystal display elements), STN-LCDs (super twisted nematic liquid crystal display elements), OCB-LCDs and IPS-LCDs (in-plane switching liquid crystal display elements), but IPS mode or FFS mode liquid crystal display elements are particularly preferred. .
Δn :295Kにおける屈折率異方性(別名:複屈折率)
Δε :295Kおける誘電率異方性
η :295Kにおける粘度(mPa・s)
γ1 :295Kにおける回転粘性(mPa・s)
VHR:周波数60Hz,印加電圧5Vの条件下で313Kにおける電圧保持率(%)
焼き付き:
液晶表示素子の焼き付き評価は、表示エリア内に所定の固定パターンを1440時間表示させた後に、全画面均一な表示を行ったときの固定パターンの残像のレベルを目視にて以下の4段階評価で行った。 Tni: Nematic phase-isotropic liquid phase transition temperature (° C)
Δn: Refractive index anisotropy at 295K (also known as birefringence)
Δε: Dielectric anisotropy at 295K η: Viscosity at 295K (mPa · s)
γ1: rotational viscosity at 295 K (mPa · s)
VHR: Voltage holding ratio (%) at 313K under conditions of frequency 60Hz and applied voltage 5V
Burn-in:
The burn-in evaluation of the liquid crystal display element is based on the following four-step evaluation of the afterimage level of the fixed pattern when the predetermined fixed pattern is displayed in the display area for 1440 hours and then the entire screen is displayed uniformly. went.
○残像ごく僅かに有るも許容できるレベル
△残像有り許容できないレベル
×残像有りかなり劣悪
揮発性/製造装置汚染性:
液晶材料の揮発性評価は、真空攪拌脱泡ミキサーの運転状態をストロボスコープで照らしながら観察し、液晶材料の発泡を目視により観察することによって行った。具体的には、容量2.0Lの真空攪拌脱泡ミキサーの専用容器に液晶組成物を0.8kg入れ、4kPaの脱気下、公転速度15S-1、自転速度7.5S-1で真空攪拌脱泡ミキサーを運転し、発泡が始まるまでの時間によって、以下の4段階評価で行った。 ◎ No afterimage ○ Very little afterimage but acceptable level △ With afterimage unacceptable level × Afterimage quite bad Volatility / contamination of manufacturing equipment:
Evaluation of the volatility of the liquid crystal material was performed by observing the operating state of the vacuum stirring and defoaming mixer with a stroboscope and visually observing foaming of the liquid crystal material. Specifically, put 0.8kg of the liquid crystal composition in a dedicated container vacuum agitation defoaming mixer having a volume 2.0L, under degassing of 4 kPa, the revolution speed 15S -1, vacuum stirring at rotation speed 7.5S -1 The defoaming mixer was operated, and the following four-step evaluation was performed according to the time until foaming started.
プロセス適合性は、ODFプロセスにおいて、定積計量ポンプを用いて1回に40pLずつ液晶を滴下することを100000回行い、次の「0~200回、201~400回、401~600回、・・・・99801~100000回」の各200回ずつ滴下された液晶量の変化を以下の4段階で評価した。 Process suitability:
The process suitability is that the liquid crystal is dropped 40 pL at a time by using a constant volume metering pump 100000 times in the ODF process, and the following “0 to 200 times, 201 to 400 times, 401 to 600 times, ..., 99801 to 100,000 times ”, the change in the amount of liquid crystal dropped 200 times was evaluated in the following four stages.
○変化が僅かに有るも許容できるレベル
△変化が有り許容できないレベル(斑発生により歩留まりが悪化)
×変化が有りかなり劣悪(液晶漏れや真空気泡が発生)
低温での溶解性:
低温での溶解性評価は、液晶組成物を調製後、1mLのサンプル瓶に液晶組成物を0.5g秤量し、これに温度制御式試験槽の中で、次を1サイクル「-20℃(1時間保持)→昇温(0.2℃/毎分)→0℃(1時間保持)→昇温(0.2℃/毎分)→20℃(1時間保持)→降温(-0.2℃/毎分)→0℃(1時間保持)→降温(-0.2℃/毎分)→-20℃」として温度変化を与え続け、目視にて液晶組成物からの析出物の発生を観察し、以下の4段階評価を行った。 ◎ Extremely small change (Stable liquid crystal display device can be manufactured)
○ Allowable level with slight change △ Level with change and unacceptable level (Yield deteriorated due to spots)
× There is a change and it is quite inferior (liquid crystal leakage and vacuum bubbles are generated)
Solubility at low temperature:
In order to evaluate the solubility at a low temperature, after preparing the liquid crystal composition, 0.5 g of the liquid crystal composition was weighed in a 1 mL sample bottle, and the next was “−20 ° C. (−20 ° C.)” in a temperature-controlled test tank. 1 hour hold) → temperature rise (0.2 ° C./min)→0° C. (1 hour hold) → temperature rise (0.2 ° C./min)→20° C. (1 hour hold) → temperature drop (−0. 2 ° C / min) → 0 ° C (hold for 1 hour) → temperature drop (−0.2 ° C / min) → −20 ° C. The following four-level evaluation was performed.
-n -CnH2n+1 炭素原子数nの直鎖状アルキル基
-On -OCnH2n+1 炭素原子数nの直鎖状アルコキシ基
-V(またはV0) -C=CH2 ビニル基
-Vn -C=C-CnH2n+1 炭素原子数(n+1)の1-アルケン
-F -F フッ素原子
F- -F フッ素原子
n- CnH2n+1- 炭素数nの直鎖状のアルキル基
nO- CnH2n+1O- 炭素数nの直鎖状のアルコキシル基
V- CH2=CH-
-V1 -CH=CH-CH3
1V- CH3-CH=CH-
-2V -CH2-CH2-CH=CH3
V2- CH3=CH-CH2-CH2-
-2V1 -CH2-CH2-CH=CH-CH3
1V2- CH3-CH=CH-CH2-CH2
-COO- -COO-(エステル基)
-CF2O- -CF2O-基
(環構造) (Side chain structure and linking structure)
-N -C n H 2n + 1 linear alkyl group with n carbon atoms -On -OC n H 2n + 1 linear alkoxy group with n carbon atoms -V (or V0) -C = CH 2 vinyl group -Vn- C = C—C n H 2n + 1 1-alkene having 1 (n + 1) carbon atoms -F 2 -F Fluorine atom F- -F Fluorine atom n- CnH 2n + 1- Linear alkyl group having n carbon atoms nO- CnH 2n + 1 O -Straight-chain alkoxyl group having n carbon atoms V- CH 2 = CH-
-V1 -CH = CH-CH 3
1V- CH 3 —CH═CH—
-2V -CH 2 -CH 2 -CH = CH 3
V2- CH 3 = CH-CH 2 -CH 2-
-2V1 -CH 2 -CH 2 -CH = CH-CH 3
1V2- CH 3 —CH═CH—CH 2 —CH 2
—COO— —COO— (ester group)
—CF 2 O— —CF 2 O— group (ring structure)
102 TFT層
103 画素電極
104 パッシベーション膜
105 第1配向膜
200 第2基板
201 平坦化膜(オーバーコート層)
202 ブラックマトリックス
203 カラーフィルタ
204 透明電極
205 第2配向膜
301 シール材
302 突起(柱状スペーサー)
303 液晶層
304 突起(柱状スペーサー)
401 マスクパターン
402 レジン層
L 光
1,8 偏光板
2 第一の基板
3 電極層
4 配向膜
5 液晶層
6 カラーフィルタ
6G カラーフィルタ緑
6R カラーフィルタ赤
7 第二の基板
11 ゲート電極
12 ゲート絶縁膜
13 半導体層
14 絶縁層
15 オーミック接触層
16 ドレイン電極
17 ソース電極
18 絶縁保護層
21 画素電極
22 共通電極
23 ストレイジキャパシタ
24 ドレイン電極
25 データ配線
27 ソース配線
29 共通ライン
30 バッファー層 100
202
303
401
Claims (7)
- 一般式(i):
で表される化合物を少なくとも1種以上と、を含有し、25℃における誘電率異方性が0より大きく5以下である液晶組成物。 General formula (i):
And a liquid crystal composition having a dielectric anisotropy at 25 ° C. of greater than 0 and 5 or less. - 一般式(M-1):
R2は、炭素原子数1~10個のアルキル基、炭素原子数2~10個のアルケニル基、炭素原子数1~10個のアルコキシ基、水素原子、フッ素原子、シアノ基、-CF3または-OCF3を表し、
環A、環Bは、それぞれ独立して、
(a) 1,4-シクロヘキシレン基(この基中に存在する1個の-CH2-又は隣接していない少なくとも2個の-CH2-は-O-に置き換えられてもよい)、及び、
(b) 1,4-フェニレン基(この基中に存在する1個の-CH=又は隣接していない少なくとも2個の-CH=は-N=に置き換えられてもよい)、
からなる群より選ばれる基を表し、上記の基(a)と基(b)は、それぞれ独立して、シアノ基、フッ素原子又は塩素原子で置換されていても良く、
nは0または1を表す。)
で表される化合物を少なくとも1種以上を、含む請求項1に記載の液晶組成物。 Formula (M-1):
R 2 represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a hydrogen atom, a fluorine atom, a cyano group, —CF 3 or Represents OCF 3 ,
Ring A and Ring B are each independently
(A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and ,
(B) a 1,4-phenylene group (one —CH═ present in this group or at least two non-adjacent —CH═ may be replaced by —N═),
Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atom or a chlorine atom,
n represents 0 or 1. )
The liquid crystal composition according to claim 1, comprising at least one compound represented by the formula: - 一般式(L):
OLは0、1、2又は3を表し、
BL1、BL2及びBL3は、それぞれ独立して、
(a) 1,4-シクロヘキシレン基(この基中に存在する1個の-CH2-又は隣接していない少なくとも2個の-CH2-は-O-に置き換えられてもよい)、及び、
(b) 1,4-フェニレン基(この基中に存在する1個の-CH=又は隣接していない少なくとも2個の-CH=は-N=に置き換えられてもよい)、
からなる群より選ばれる基を表し、上記の基(a)と基(b)は、それぞれ独立して、シアノ基、フッ素原子又は塩素原子で置換されていても良く、
LL1及びLL2は、それぞれ独立して、単結合、-CH2CH2-、-(CH2)4-、-OCH2-、-CH2O-、-COO-、-OCO-、-OCF2-、-CF2O-、-CH=N-N=CH-、-CH=CH-、-CF=CF-又は-C≡C-を表し、
OLが2又は3であってLL2が複数存在する場合は、それらは同一であっても異なっていても良く、OLが2又は3であってBL3が複数存在する場合は、それらは同一であっても異なっていても良いが、前記一般式(i)および前記一般式(M-1)で表される化合物を除く)
で表される少なくとも1種の化合物を更に含有する請求項1に記載の液晶組成物。 Formula (L):
OL represents 0, 1, 2 or 3;
B L1 , B L2 and B L3 are each independently
(A) 1,4-cyclohexylene group (this is present in the group one -CH 2 - or non-adjacent at least two -CH 2 - may be replaced by -O-), and ,
(B) a 1,4-phenylene group (one —CH═ present in this group or at least two non-adjacent —CH═ may be replaced by —N═),
Each of the groups (a) and (b) may be independently substituted with a cyano group, a fluorine atom or a chlorine atom,
L L1 and L L2 each independently represent a single bond, —CH 2 CH 2 —, — (CH 2 ) 4 —, —OCH 2 —, —CH 2 O—, —COO—, —OCO—, — OCF 2 -, - CF 2 O -, - CH = N-N = CH -, - CH = CH -, - represents CF = CF- or -C≡C-,
When OL is 2 or 3 and a plurality of L L2 are present, they may be the same or different, and when OL is 2 or 3 and a plurality of B L3 is present, they are the same Or may be different, except for the compounds represented by the general formula (i) and the general formula (M-1))
The liquid crystal composition according to claim 1, further comprising at least one compound represented by: - 一般式(M):
PMは、0、1、2、3又は4を表し、
CM1及びCM2は、それぞれ独立して、
(d) 1,4-シクロヘキシレン基(この基中に存在する1個の-CH2-又は隣接していない少なくとも2個の-CH2-は-O-又は-S-に置き換えられてもよい)、及び、
(e) 1,4-フェニレン基(この基中に存在する1個の-CH=又は隣接していない少なくとも2個の-CH=は-N=に置き換えられてもよい)、
からなる群より選ばれる基を表し、上記の基(d)と基(e)は、それぞれ独立して、シアノ基、フッ素原子又は塩素原子で置換されていても良く、
KM1及びKM2は、それぞれ独立して、単結合、-CH2CH2-、-(CH2)4-、-OCH2-、-CH2O-、-OCF2-、-CF2O-、-COO-、-OCO-又は-C≡C-を表し、
PMが2、3又は4であってKM1が複数存在する場合は、それらは同一であっても異なっていても良く、PMが2、3又は4であってCM2が複数存在する場合は、それらは同一であっても異なっていても良く、
XM1及びXM3は、それぞれ独立して、水素原子、塩素原子又はフッ素原子を表し、
XM2は、水素原子、フッ素原子、塩素原子、シアノ基、トリフルオロメチル基、フルオロメトキシ基、ジフルオロメトキシ基、トリフルオロメトキシ基又は2,2,2-トリフルオロエチル基を表すが、前記一般式(i)、前記一般式(M-1)および一般式(L)で表される化合物を除く)
で表される少なくとも1種の化合物を更に含有する請求項1又は2に記載の液晶組成物。 General formula (M):
PM represents 0, 1, 2, 3 or 4;
C M1 and C M2 are each independently
(D) a 1,4-cyclohexylene group (in which one —CH 2 — or at least two adjacent —CH 2 — groups may be replaced by —O— or —S—). Good) and
(E) a 1,4-phenylene group (one —CH═ present in this group or at least two non-adjacent —CH═ may be replaced by —N═),
The group (d) and the group (e) are each independently substituted with a cyano group, a fluorine atom or a chlorine atom,
K M1 and K M2 each independently represent a single bond, —CH 2 CH 2 —, — (CH 2 ) 4 —, —OCH 2 —, —CH 2 O—, —OCF 2 —, —CF 2 O -, -COO-, -OCO- or -C≡C-
When PM is 2, 3 or 4 and there are a plurality of K M1 , they may be the same or different, and when PM is 2, 3 or 4 and there are a plurality of C M2 They may be the same or different,
X M1 and X M3 each independently represent a hydrogen atom, a chlorine atom or a fluorine atom,
X M2 represents a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, a trifluoromethyl group, a fluoromethoxy group, a difluoromethoxy group, a trifluoromethoxy group, or a 2,2,2-trifluoroethyl group, (Excluding compounds represented by formula (i), general formula (M-1) and general formula (L))
The liquid crystal composition according to claim 1, further comprising at least one compound represented by the formula: - 請求項1~4のいずれか1項に記載の液晶組成物を使用した液晶表示素子。 A liquid crystal display element using the liquid crystal composition according to any one of claims 1 to 4.
- 請求項1~4のいずれか1項に記載の液晶組成物を使用したことを特徴とするIPSモード、OCBモード、ECBモード、VAモード又はFFSモード用液晶表示素子。 5. A liquid crystal display element for IPS mode, OCB mode, ECB mode, VA mode or FFS mode, wherein the liquid crystal composition according to claim 1 is used.
- 請求項5又は6に記載の液晶表示素子を使用したことを特徴とする液晶表示ディスプレイ。 A liquid crystal display using the liquid crystal display element according to claim 5.
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