Disclosure of Invention
The invention aims to provide a liquid crystal composition which has the characteristics of wide nematic phase temperature range, proper optical anisotropy, high dielectric anisotropy, high clearing point, low threshold voltage and low viscosity. The display using the liquid crystal composition of the present invention has a fast response and excellent power saving performance.
The technical scheme adopted by the invention is to provide a liquid crystal composition, which comprises the following components in part by weight:
1-15% by weight of a compound of the formula I
5-35% by weight of a compound of the formula II
1 to 20% by weight of a compound of the formula III
5-55% by weight of a compound of the formula IV
20-70% by weight of a compound of formula V:
wherein,
R1、R2、R3and R4The same or different, each independently represents H, an alkyl group or an alkoxy group having 1 to 5 carbon atoms, or an alkenyl group having 2 to 5 carbon atoms;
R5and R6The same or different, each independently represents an alkyl group or an alkoxy group having 1 to 5 carbon atoms, or an alkenyl group having 2 to 5 carbon atoms;
to represent Wherein saidTo the lastOne or more H may be substituted by F;
are the same or different and each independently represents
Are the same or different and each independently represents
X1Represents an alkyl group having 1 to 5 carbon atoms or a halogen;
X2represents halogen or-OCF3;
L1And L2The same or different, each independently represents H or F;
Z1represents-CH2CH2-or a single bond;
Z2represents-COO-or a single bond;
m represents 0 or 1;
n represents 1 or 2; and when n is 2, the compound is,may be the same or different;
p represents 0, 1 or 2.
In some embodiments, R1And R3The alkyl groups may be the same or different and each independently represents an alkyl group having 1 to 5 carbon atoms.
In some embodiments, R2Represents H or an alkyl group having 1 to 5 carbon atoms.
In some embodiments, R4Represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms.
In some embodiments of the present invention, the substrate is,to represent In some embodiments, it is preferred that,to represent
In some embodiments of the present invention, the substrate is,to representIn some embodiments, it is preferred that,to represent
In some embodiments of the present invention, the substrate is,to represent
In some embodiments of the present invention, the substrate is,to represent
In some embodiments of the present invention, the substrate is,to representIn some embodiments, it is preferred that,to represent
In some embodiments, X1Represents an alkyl group having 2 to 4 carbon atoms or a halogen. In some embodiments, preferably, X1Represents halogen. In some embodiments, preferably, the halogen is F. Preferably, X1Represents an alkyl group having 2 to 5 carbon atoms or F.
In some embodiments, X2Represents F or-OCF3。
In some embodiments, Z1Represents a single bond.
In some embodiments, R4Represents an alkyl group having 1 to 5 carbon atoms.
In some embodiments, R5Represents an alkyl group having 1 to 5 carbon atoms.
In some embodiments, R6Represents an alkane having 1 to 5 carbon atomsA group or an alkenyl group having 2 to 5 carbon atoms.
In some embodiments of the present invention, the substrate is,to represent
In some embodiments, Z2Represents a single bond.
In some embodiments of the present invention, the substrate is,to representIn some embodiments, it is preferred that,to represent
In some embodiments, p represents 0 or 2.
In some embodiments of the present invention, preferably, the compound of formula i comprises 3 to 10% by weight of the total liquid crystal composition; the compound of the general formula II accounts for 10-30% of the total weight of the liquid crystal composition; the compound of the general formula III accounts for 1-15% of the total weight of the liquid crystal composition; the compound of the general formula IV accounts for 5-50% of the total weight of the liquid crystal composition; and the compound of the general formula V accounts for 25-65% of the total weight of the liquid crystal composition.
In some embodiments of the invention, the compound of formula i is selected from the group consisting of:
in some embodiments of the invention, the compound of formula ii is selected from the group consisting of:
in some embodiments, especially preferred are compounds of formulae II-1, II-5, II-8, II-9, II-10, and II-11.
In some embodiments of the present invention, preferably, the compound of formula II-1 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-2 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-3 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-4 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-5 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-6 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-7 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-8 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-9 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-10 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula ii-11 is selected from the group consisting of:
as a particularly preferred embodiment, the compound of formula ii is selected from the group consisting of:
in some embodiments of the invention, the compound of formula iii is selected from the group consisting of:
in some embodiments, especially preferred are compounds of formulae III-6 to III-9.
In some embodiments of the invention, the compound of formula iv is selected from the group consisting of:
in some embodiments, particularly preferred are compounds of formulae IV-1 to IV-3, IV-5 to IV-8.
In some embodiments of the present invention, preferably, the compound of formula IV-1 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-2 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-3 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-4 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-5 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-6 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-7 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-8 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-9 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-10 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula IV-11 is selected from the group consisting of:
as a particularly preferred embodiment, the compound of formula iv is selected from the group consisting of:
in some embodiments of the invention, the compound of formula v is selected from the group consisting of:
in some embodiments, especially preferred are compounds of formula V-1, V-4 to V-7.
In some embodiments of the present invention, preferably, the compound of formula v-1 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula v-2 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula v-3 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula v-4 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula v-5 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula v-6 is selected from the group consisting of:
in some embodiments of the present invention, preferably, the compound of formula v-7 is selected from the group consisting of:
as a particularly preferred embodiment, the compound of formula v is selected from the group consisting of:
according to another aspect of the present invention, there is also provided a liquid crystal display comprising the liquid crystal composition provided by the present invention.
By adopting the technical scheme, compared with the prior art, the invention has the following technical effects:
the liquid crystal composition provided by the invention has the characteristics of wider nematic phase temperature range, proper optical anisotropy, higher dielectric anisotropy, higher clearing point, low threshold voltage, low viscosity and the like; when the liquid crystal composition is applied to a liquid crystal display device, the liquid crystal display device can have quick response and excellent electricity-saving performance.
Unless otherwise stated, the ratios described in the present invention are weight ratios, all temperatures are in degrees celsius, and the test of the response time data has a box thickness of 7 μm.
Detailed Description
The invention will be illustrated below with reference to specific embodiments. It should be noted that the following examples are illustrative of the present invention, and are not intended to limit the present invention. Other combinations and various modifications within the spirit or scope of the present invention may be made without departing from the spirit or scope of the present invention.
For convenience of expression, in the following examples, the group structure of the liquid crystal composition is represented by the code listed in Table 1:
TABLE 1 radical structural code of liquid crystal compounds
Compounds of the following formula are exemplified:
the structural formula is represented by the code listed in Table 2, and can be expressed as: nCPUF, where n in the code represents the number of C atoms in the left alkyl group, e.g. n is"3" means that the alkyl group is-C3H7(ii) a C in the code represents cyclohexane.
The abbreviated codes of the test items in the following examples are as follows:
cp (. degree. C.): clearing points (transition temperature of liquid crystal from nematic phase to isotropic phase)
Δ n: optical anisotropy (589nm, 25 ℃ C.)
Δ ε: dielectric anisotropy (1KHz, 25 ℃ C.)
V10: threshold voltage (characteristic voltage at 10% relative contrast, normally white mode)
V90: saturation voltage (characteristic voltage at 90% relative contrast, normally white mode)
eta.flow viscosity (mm)2·s-125 ℃ unless otherwise stated)
TN-S(° c): transition temperature of liquid crystal from nematic phase to smectic phase
Wherein the refractive index anisotropy is obtained by testing an Abbe refractometer under a sodium lamp (589nm) light source at 25 ℃; the dielectric test cell was of the type TN90, the cell thickness being 7 μm.
and the testing condition is that the temperature is 25 ℃, the temperature is 1KHz, the testing box is TN90 type, and the box thickness is 7 mu m.
The components used in the following examples can be synthesized by a known method or obtained commercially. These synthesis techniques are conventional, and the resulting liquid crystal compounds were tested to meet the standards for electronic compounds.
Liquid crystal compositions were prepared according to the compounding ratios of the liquid crystal compositions specified in the following examples. The liquid crystal composition is prepared according to the conventional method in the field, such as heating, ultrasonic wave, suspension and the like, and is mixed according to the specified proportion.
Comparative example 1
The liquid crystal composition of comparative example 1, which was filled between two substrates of a liquid crystal display and subjected to a performance test, was prepared according to the compounds and weight percentages listed in table 2, and the test data are shown in the following table:
TABLE 2 liquid crystal composition formulations and their test properties
Comparative example 2
The liquid crystal composition of comparative example 2, which was filled between two substrates of a liquid crystal display and subjected to a performance test, was prepared according to the compounds and weight percentages listed in table 3, and the test data are shown in the following table:
TABLE 3 liquid crystal composition formula and its test performance