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KR20030033770A - Liquid crystal having high speed and high temperature using liquid crystal mixture of fluoroisothionate - Google Patents

Liquid crystal having high speed and high temperature using liquid crystal mixture of fluoroisothionate Download PDF

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KR20030033770A
KR20030033770A KR1020010065884A KR20010065884A KR20030033770A KR 20030033770 A KR20030033770 A KR 20030033770A KR 1020010065884 A KR1020010065884 A KR 1020010065884A KR 20010065884 A KR20010065884 A KR 20010065884A KR 20030033770 A KR20030033770 A KR 20030033770A
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South Korea
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liquid crystal
formula
nematic liquid
crystal composition
nematic
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KR1020010065884A
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Korean (ko)
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반병섭
윤용국
서봉성
김봉희
사공동식
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삼성전자주식회사
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Priority to KR1020010065884A priority Critical patent/KR20030033770A/en
Priority to EP02724797A priority patent/EP1438371A4/en
Priority to JP2003538302A priority patent/JP2005506440A/en
Priority to PCT/KR2002/000768 priority patent/WO2003035798A1/en
Priority to US10/493,717 priority patent/US20050062018A1/en
Priority to CNA028262379A priority patent/CN1608119A/en
Publication of KR20030033770A publication Critical patent/KR20030033770A/en
Priority to US11/399,925 priority patent/US20060177604A1/en

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    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
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    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
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    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
    • C09K19/3001Cyclohexane rings
    • C09K19/3066Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers
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    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
    • C09K19/3001Cyclohexane rings
    • C09K19/3003Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
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    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
    • C09K19/3001Cyclohexane rings
    • C09K19/3003Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
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    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
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    • C09K19/3001Cyclohexane rings
    • C09K19/3028Cyclohexane rings in which at least two rings are linked by a carbon chain containing carbon to carbon single bonds
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    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
    • C09K19/3001Cyclohexane rings
    • C09K19/3066Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers
    • C09K19/3068Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers chain containing -COO- or -OCO- groups
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  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

PURPOSE: Provided is a nematic liquid crystal composition having high phase transition temperature of liquid crystals and high response velocity, which can be used for preparing LCD elements. CONSTITUTION: The nematic liquid crystal composition contains: 2-80wt% of a nematic liquid crystal compound represented by the formula 1 or nematic liquid crystal compounds represented by the formula 2 and 3, wherein the weight ratio of the compound represented by the formula 2 and the compound represented by the formula 3 is 1-80:1-80; 20-98wt% of at least one liquid crystal compound selected from the compounds represented by the formula 4, 5, and 6, wherein R2 and R3 are independently or simultaneously C1-C15 alkyl or alkoxy, B is phenyl or cyclohexyl, C is a single bond, -CH2CH2-, or -COO-, X and Y are independently or simultaneously hydrogen or fluoro atom, and Z is hydrogen, -OCF3, or fluoro atom.

Description

플루오로아이소사이오네이트의 액정혼합물을 이용한 고속 고온 액정{LIQUID CRYSTAL HAVING HIGH SPEED AND HIGH TEMPERATURE USING LIQUID CRYSTAL MIXTURE OF FLUOROISOTHIONATE}LIQUID CRYSTAL HAVING HIGH SPEED AND HIGH TEMPERATURE USING LIQUID CRYSTAL MIXTURE OF FLUOROISOTHIONATE}

본 발명은 플루오로아이소사이오네이트의 액정혼합물을 이용한 고속 고온 액정에 관한 것으로, 더욱 상세하게는 상전이 온도와 응답속도를 향상시킬 수 있는 네마틱 액정 화합물을 포함하는 고속 고온 액정 조성물에 관한 것이다.The present invention relates to a high speed high temperature liquid crystal using a liquid crystal mixture of fluoroisocyionate, and more particularly, to a high speed high temperature liquid crystal composition including a nematic liquid crystal compound capable of improving phase transition temperature and response speed.

디스플레이 분야에서 TN-LCD(Twist Nematic-Liquid Crystal Display)는 영역이 지속적으로 확대되어 왔으며, 그 범위로 노트북, 모니터는 물론 가정용 TV, 중소형 쪽으로 영역을 확대하고 있다.In the field of display, Twist Nematic-Liquid Crystal Display (TN-LCD) has been continuously expanding its scope, and is expanding its scope to notebooks, monitors, home TVs, and small and medium-sized enterprises.

상기 LCD는 경박단소의 물리적 장점을 지니고 있으나 화질을 결정하는 여러 가지 인자들 중에서 휘도 등은 CRT(Cathod Ray Tube)에 비해 취약한 문제가 있다. 또한, 모니터 및 새로운 LCD의 큰 시장으로 주목받는 LCD-TV의 시장이 점차 형성되고 확산되면서 고휘도 및 고속응답기술에 대한 요구가 매우 중요한 사항으로 대두되고 있다.The LCD has a physical advantage of light and thin, but there is a problem that the brightness is weaker than the CRT (Cathod Ray Tube) among the various factors that determine the image quality. In addition, as the LCD-TV market, which is attracting attention as a large market for monitors and new LCDs, is gradually formed and spread, the demand for high brightness and high-speed response technology is emerging as an important matter.

LCD에서 고휘도를 얻기 위해서는 백라이트에 관전류 등으로 인해 액정의 상전이 온도가 현행보다 높게 유지되어야 한다. 또한, 고속응답을 위해서는 물질의 회전 점도를 줄이거나 액정의 굴절률을 크게 하는 방안 등이 있다.In order to obtain high brightness in LCD, the liquid crystal phase transition temperature must be kept higher than the current due to tube current. In addition, for high-speed response, there is a method of reducing the rotational viscosity of the material or increasing the refractive index of the liquid crystal.

현재까지 제품화되고 있는 LCD 제품은 대부분이 TN, IPS, VA 모드로서 네마틱 액정을 사용하고 있으며, 상전이 온도는 70 내지 80 ℃정도이고, 응답속도는 20 내지 30 ms 정도이다. 그러나, 상기 상전이 온도 및 응답속도는 여전히 만족스럽지 못하기 때문에, TV 응용 및 동화상을 실현하기 위해서는 응답속도의 개선 및 상전이 온도의 증가가 절실히 요구되어지고 있다.Most LCD products that have been commercialized so far use nematic liquid crystals as TN, IPS, and VA modes, and have a phase transition temperature of about 70 to 80 ° C. and a response speed of about 20 to 30 ms. However, since the phase transition temperature and the response speed are still not satisfactory, the improvement of the response speed and the increase of the phase transition temperature are urgently required to realize TV applications and moving images.

본 발명은 상기와 같은 종래 기술의 문제점을 고려하여, 액정의 상전이 온도가 높으며 고속의 응답속도를 실현할 수 있는 네마틱 액정 조성물을 제공하는 것을 목적으로 한다.SUMMARY OF THE INVENTION In view of the problems of the prior art as described above, an object of the present invention is to provide a nematic liquid crystal composition having a high phase transition temperature and realizing a high response speed.

본 발명의 다른 목적은 상기 고속 고온 네마틱 액정 조성물을 포함하여 제조되는 LCD 소자를 제공하는 것이다.Another object of the present invention is to provide an LCD device manufactured by including the high speed high temperature nematic liquid crystal composition.

상기 목적을 달성하기 위하여, 본 발명은 하기 화학식 1로 표시되는 네마틱 액정 화합물을 포함하는 네마틱 액정 조성물을 제공한다.In order to achieve the above object, the present invention provides a nematic liquid crystal composition comprising a nematic liquid crystal compound represented by the following formula (1).

[화학식 1][Formula 1]

또한, 본 발명은 하기 화학식 2 및 3으로 표시되는 네마틱 액정 화합물을 포함하는 네마틱 액정 조성물을 제공한다.In addition, the present invention provides a nematic liquid crystal composition comprising a nematic liquid crystal compound represented by the following formulas (2) and (3).

[화학식 2][Formula 2]

[화학식 3][Formula 3]

이하에서 본 발명을 상세하게 설명한다.Hereinafter, the present invention will be described in detail.

본 발명자들은 종래 네마틱 액정 조성물에서의 문제점을 해결하고자, 고휘도와 고속응답기술을 목표로 액정의 상전이 온도를 높이고, 굴절률 이방성 증가 등으로 고온고속액정 개발을 통한 고속 응답기술을 실현할 수 있는 상기 화학식 1의 화합물을 포함하는 액정 조성물을 개발하여 본 발명을 완성하였다.The inventors of the present invention can solve the problems in the conventional nematic liquid crystal composition, to achieve the high-speed response technology through the development of high-temperature high-speed liquid crystal by increasing the phase transition temperature of the liquid crystal, the refractive index anisotropy, etc. aiming at high brightness and high speed response technology The liquid crystal composition containing the compound of 1 was developed, and this invention was completed.

본 발명의 네마틱 액정 조성물은 종래 상용 액정 조성물에 주요성분(Key material)으로 특정 네마틱 혼합물을 블렌딩함으로써 기존 상용 액정에 비해 온도를 적어도 10 ℃ 이상을 높이고, 응답속도를 10 ms 정도로 실현할 수 있다.According to the nematic liquid crystal composition of the present invention, by blending a specific nematic mixture with a key material in a conventional commercial liquid crystal composition, the temperature may be increased by at least 10 ° C. or more, and the response speed may be about 10 ms compared to conventional commercial liquid crystals. .

본 발명의 네마틱 액정 조성물은 적어도 2 종 이상의 액정 화합물을 포함하는 것이 바람직하다.It is preferable that the nematic liquid crystal composition of this invention contains a 2 or more types of liquid crystal compound.

본 발명의 네마틱 액정 조성물은 상기 화학식 1의 화합물을 포함한다. 또한, 본 발명의 네마틱 액정 조성물은 상기 화학식 2 및 화학식 3의 화합물을 포함한다. 상기 화학식 1의 화합물, 또는 화학식 2 및 3의 혼합물의 사용량은 2 내지 80 중량%인 것이 바람직하다. 이때, 상기 화학식 1의 화합물, 또는 화학식 2 및 3의 혼합물의 사용량이 상기 범위를 벗어나면 높은 상전이 온도와 고속의 응답속도를 얻을 수 없는 문제가 있다. 상기 화학식 2 및 3의 화합물의 혼합비율은 1 내지 80 : 1 내지 80의 중량비로 혼합 사용하는 것이 바람직하다.The nematic liquid crystal composition of the present invention includes the compound of Formula 1. In addition, the nematic liquid crystal composition of the present invention includes the compound of Formula 2 and Formula 3. The amount of the compound of Formula 1 or a mixture of Formulas 2 and 3 is preferably 2 to 80% by weight. At this time, when the amount of the compound of Formula 1 or the mixture of Formulas 2 and 3 is out of the range, there is a problem that a high phase transition temperature and a high response speed cannot be obtained. The mixing ratio of the compounds of Formulas 2 and 3 is preferably used in a weight ratio of 1 to 80: 1 to 80.

또한, 본 발명의 액정 조성물은 상기 화학식 1의 화합물과 함께 적어도 1 종 이상의 상용의 액정 화합물을 포함한다. 또한, 본 발명의 액정 조성물은 상기 화학식 2 및 3의 화합물과 함께 적어도 1 종 이상의 액정 화합물을 포함한다. 상기 상용의 액정 화합물은 하기 화학식 4, 화학식 5 및 화학식 6으로 표시되는 화합물로 이루어진 군으로부터 선택되는 적어도 1 종 이상의 액정 화합물을 사용하는 것이 바람직하다. 본 발명의 네마틱 액정 조성물은 상용의 액정 화합물을 20 내지 98 중량% 포함하는 것이 바람직하다.In addition, the liquid crystal composition of the present invention includes at least one or more commercially available liquid crystal compounds together with the compound of Formula 1. In addition, the liquid crystal composition of the present invention includes at least one or more liquid crystal compounds together with the compounds of Formulas 2 and 3. It is preferable to use at least one liquid crystal compound selected from the group consisting of compounds represented by the following general formulas (4), (5) and (6) as the commercially available liquid crystal compound. It is preferable that the nematic liquid crystal composition of this invention contains 20 to 98 weight% of a commercial liquid crystal compound.

[화학식 4][Formula 4]

[화학식 5][Formula 5]

[화학식 6][Formula 6]

상기 식에서, R2및 R3는 각각 독립적으로 또는 동시에 탄소수 1 내지 15의 알킬기 또는 알콕시기이며; B는 페닐 또는 사이클로헥실이며; C는 단일결합, -CH2CH2-, 또는 -COO- 이며; X 및 Y는 각각 독립적으로 또는 동시에 수소 또는 플르오로 원자이며; Z는 수소, -OCF3또는 플루오로원자이다.Wherein R 2 and R 3 are each independently or simultaneously an alkyl or alkoxy group having 1 to 15 carbon atoms; B is phenyl or cyclohexyl; C is a single bond, -CH 2 CH 2- , or -COO-; X and Y are each independently or simultaneously hydrogen or fluoro atoms; Z is hydrogen, -OCF 3 or a fluoro atom.

본 발명에서 사용하는 상용 액정 화합물은 상기 화학식 3, 화학식 4 및 화학식 5의 화합물의 조합에 의해 사용할 수 있으며, 그 바람직한 일 실시예를 들면, 상용의 액정 화합물은 화학식 4 내지 6의 화합물 중에서 4개의 군(G1 내지 G4)으로 나누어 혼합 사용하는 것이 더욱 바람직하다. 상기 G1 내지 G4의 구성은 G1 10 내지 25 중량, G2 10 내지 20 중량%, G3 30 내지 40 중량% 및 G4 20 내지 40 중량%로 혼합하는 것이 좋다. 상기 G1 군은 상기 화학식 5 및 6의 화합물 군으로부터 선택되는 적어도 2 종 이상의 화합물이고; G2는 상기 화학식 4 및 화학식 5의 화합물 군으로부터 선택되는 적어도 2 종 이상의 화합물이고; 상기 G3은 화학식 5 및 6의 화합물 군으로부터 선택되는 적어도 2 종 이상의 화합물이고; 및 상기 G4는 화학식 4의 화합물 군으로부터 선택되는 적어도 2 종 이상의 화합물인 것이 바람직하다.The commercially available liquid crystal compound used in the present invention may be used by a combination of the compounds of Formulas 3, 4, and 5, and, for example, a commercially available liquid crystal compound may be selected from four compounds of Formulas 4-6. It is more preferable to divide into groups (G1 to G4) and use them. The composition of the G1 to G4 is preferably mixed with 10 to 25% by weight of G1, 10 to 20% by weight of G2, 30 to 40% by weight of G3 and 20 to 40% by weight of G4. The G1 group is at least two or more compounds selected from the group of compounds represented by Formulas 5 and 6 above; G2 is at least two or more compounds selected from the group of compounds represented by formulas (4) and (5); G3 is at least two or more compounds selected from the group of compounds represented by Formulas 5 and 6; And G4 is at least two or more compounds selected from the group of compounds represented by formula (4).

이와 같은 본 발명의 네마틱 액정 조성물은 복굴절율(Δn), 및 유전율이방성 (Δε) 등의 물성이 우수하며, 특히 상전이 온도가 높고 응답속도가 빠르다. 따라서, 본 발명의 고속 고온의 액정 조성물은 액정을 필요로 하는 여러 가지 LCD 제품군의 소자, 바람직하게는 트위스트 네마틱(TN) 디바이스 장치, 수퍼 트위스트 네마틱(STN) 디바이스 장치, 박막트랜지스터-트위스트 네마틱(TFT-TN) 디바이스 장치, IPS(In plane switching) 디바이스 장치, AOC(Array on color filter), COA(Color filter on array) 디바이스 장치 등의 제조에 사용하여 고휘도 및 고속응답기술 등의 물성을 가지는 LCD를 얻을 수 있다.Such nematic liquid crystal composition of the present invention is excellent in physical properties such as birefringence (Δn), dielectric anisotropy (Δε), in particular, the phase transition temperature is high and the response speed is fast. Accordingly, the high-speed, high-temperature liquid crystal composition of the present invention is a device of various LCD families requiring liquid crystal, preferably a twisted nematic (TN) device device, a super twisted nematic (STN) device device, a thin film transistor-twisted nema It is used to manufacture TFT-TN device, IPS (In plane switching) device device, AOC (Array on color filter), COA (Color filter on array) device device, etc. Branches can obtain LCD.

이하, 본 발명의 실시예 및 비교예를 기재한다. 그러나, 하기 실시예는 본 발명을 예시하는 것으로서 본 발명을 한정하는 것은 아니다.Hereinafter, the Example and comparative example of this invention are described. However, the following examples illustrate the present invention and do not limit the present invention.

[비교예 1]Comparative Example 1

하기 표 1과 같이 구성된 상용의 혼합물 "TM1"을 제조하였다(TM1 = G1+ G2+ G3+ G4). 각 G1 내지 G4의 함량은 중량%를 나타낸다.A commercial mixture "TM1" constructed as shown in Table 1 below was prepared (TM1 = G1 + G2 + G3 + G4). The content of each G1 to G4 represents weight percent.

화합물compound 함량(중량%)Content (% by weight) G1(X는 F)G1 (X is F) 3.43.4 10.010.0 10.410.4 G2G2 2.52.5 2.62.6 7.47.4 G3G3 7.07.0 3.53.5 3.973.97 11.0711.07 G4G4 20.820.8 5.365.36 6.66.6 5.45.4

상기 표 1의 TM1으로 구성된 액정혼합물은 현재 상용화되고 있는 액정으로 액정의 응답속도는 셀갭 4.6 ㎛에서 16 ∼ 18 ms로 측정되었으며, 상전이 온도는 80 ℃ 였다.The liquid crystal mixture composed of TM1 of Table 1 is a commercially available liquid crystal, and the response speed of the liquid crystal was measured to be 16 to 18 ms at a cell gap of 4.6 μm, and the phase transition temperature was 80 ° C.

[실시예 1 내지 4][Examples 1 to 4]

고온고속응답 대응의 물성 변화를 확인하기 위해, 주요성분(key material)으로 하기 표 2와 같은 함량의 상전이온도가 높고 굴절률 이방성이 큰 하기 화학식 1의 화합물과 나머지 함량의 상기 비교예 1의 혼합액정 TM1을 혼합하여 %농도에 따라 액정의 상전이온도, 굴절률이방성, 유전율이방성, 응답속도(셀갭 3.77 ㎛)를 측정하였고, 그 결과를 하기 표 2에 나타내었다.In order to confirm the change in physical properties corresponding to the high temperature high-speed response, the mixed liquid crystal of the compound of formula 1 and the remaining content of the compound of formula 1 having a high phase transition temperature and a high refractive index anisotropy as shown in Table 2 as key ingredients TM1 was mixed and the phase transition temperature, refractive index anisotropy, dielectric anisotropy, and response speed (cell gap 3.77 μm) of the liquid crystals were measured according to the% concentration, and the results are shown in Table 2 below.

[화학식 1][Formula 1]

함량(중량%)Content (% by weight) Tni (℃)Tni (℃) △ n△ n Δε(20 ℃)Δε (20 ° C) 응답속도(ms)Response speed (ms) 비교예 1Comparative Example 1 -- 8080 0.07730.0773 5.95.9 16∼1816-18 실시예 1Example 1 1414 9393 0.09820.0982 7.57.5 9.79.7 실시예 2Example 2 16.716.7 96/98.396 / 98.3 0.1027(20℃)/0.0907(28℃)0.1027 (20 ℃) /0.0907 (28 ℃) 7.8(20℃)/6.01(28℃)7.8 (20 ℃) /6.01 (28 ℃) 10.210.2 실시예 3Example 3 2020 9999 0.10820.1082 8.28.2 10.310.3 실시예 4Example 4 2626 104104 0.11810.1181 8.98.9 10.710.7 **분모:실측치 예- 96℃(계산치)/98.3℃(실측치)** Denominator: Actual value example-96 ° C (calculated) /98.3°C (actually measured)

상기 표 2에서 보면, 상기 화학식 1의 화합물이 전혀 없는 비교예 1(TM1) 대비 실시예 1 내지 4의 경우 모두 우수한 결과를 얻었으며, 특히 응답속도는 56%로 줄었고 상전이 온도는 122%로 증가하였으며, 이는 고속 고온액정으로 사용하기에 효과적임을 나타낸다.In Table 2, all of the Examples 1 to 4 compared to Comparative Example 1 (TM1) without the compound of Formula 1 obtained excellent results, in particular, the response rate was reduced to 56% and phase transition temperature increased to 122% This indicates that it is effective for use as a high speed hot liquid crystal.

[실시예 5]Example 5

상기 실시예 1 내지 4의 화학식 1 대신 하기 화학식 2 및 3의 화합물을 주요성분(key material)로 사용하여 액정의 상전이온도, 굴절률 이방성, 유전율이방성, 응답속도 (셀갭 3.75 ㎛)를 측정하였다. 즉, TM1 79.7 중량%, 화학식 2의 화합물 10.2 중량% 및 화학식 3의 화합물 10.1 중량%를 혼합하였다. 그 결과는 하기와 같다.Instead of Formula 1 of Examples 1 to 4, the compounds of Formulas 2 and 3 were used as key materials to measure phase transition temperature, refractive index anisotropy, dielectric anisotropy, and response speed (cell gap 3.75 μm) of the liquid crystal. That is, 79.7 wt% TM1, 10.2 wt% compound of formula 2 and 10.1 wt% compound of formula 3 were mixed. The result is as follows.

[화학식 2][Formula 2]

[화학식 3][Formula 3]

액정상 온도범위: -30℃∼103℃, △n:0.0952(28℃), Δε: 6.17(28℃),Liquid crystal phase temperature range: -30 ° C to 103 ° C, Δn: 0.0952 (28 ° C), Δε: 6.17 (28 ° C),

응답속도: 10.8 ms, Vth: 1.6v(28℃), VHR: 98%Response time: 10.8 ms, Vth: 1.6v (28 ℃), VHR: 98%

상기 결과에서 보면 TM1 대비 응답속도가 59%로 줄었으며 상전이 온도는 127%로 증가하여 고속 고온액정으로 사용하기에 효과적임을 알 수 있다. 기존 보고된 NCS 혼합물은 상전이 온도, 굴절율이방성 및 응답속도가 Tni: 71℃, △n: 0.15, 응답속도: 14.6 ms로 이 경우 상전이 온도가 낮고 굴절율이 높아 제품화가 어려우며, 또한 Tni: 95℃, △n: 0.089, 및 응답속도: 21.3 ms인 경우는 응답속도가 느려 동화상 대응의 고속고온 액정으로는 적용하기 어려운 점이 있다. 반면, 본 발명의 상기 실시예들은 동화상 대응의 고속 고온의 2가지를 동시에 충족시켜 주므로 제품화 가능성이 매우 높다.In the results, the response speed is reduced to 59% compared to TM1 and the phase transition temperature is increased to 127%, it can be seen that it is effective to use as a high-speed hot liquid crystal. The previously reported NCS mixture has a phase transition temperature, refractive index anisotropy and response rate of Tni: 71 ° C., Δn: 0.15, response rate of 14.6 ms. In this case, low phase transition temperature and high refractive index are difficult to commercialize, and Tni: 95 ° C., When Δn: 0.089 and response speed: 21.3 ms, the response speed is slow, which makes it difficult to apply to high-speed high-temperature liquid crystal for moving picture. On the other hand, the above-described embodiments of the present invention satisfy both of high speed and high temperature corresponding to moving images at the same time, and thus have a high possibility of commercialization.

이상에서 설명한 바와 같이, 본 발명에 따른 네마틱 액정 조성물은 상기 화학식 1의 화합물, 또는 화학식 2 및 3의 화합물을 포함하여 상용의 혼합 액정에 비해 상전이온도, 굴절률 이방성, 유전율 이방성이 크며, 응답속도가 매우 빠르므로 LCD 제조시 사용하기에 효과적이다.As described above, the nematic liquid crystal composition according to the present invention has a larger phase transition temperature, refractive index anisotropy, dielectric constant anisotropy, and response speed than a commercially available mixed liquid crystal including the compound of Formula 1 or the compounds of Formulas 2 and 3 above. Is very fast and effective for use in LCD manufacturing.

Claims (10)

하기 화학식 1로 표시되는 네마틱 액정 화합물을 포함하는 네마틱 액정 조성물:A nematic liquid crystal composition comprising the nematic liquid crystal compound represented by Formula 1 below: [화학식 1][Formula 1] 하기 화학식 2 및 3으로 표시되는 네마틱 액정 화합물을 포함하는 네마틱 액정 조성물:Nematic liquid crystal composition comprising a nematic liquid crystal compound represented by the formula (2) and [화학식 2][Formula 2] [화학식 3][Formula 3] 제 1 항에 있어서,The method of claim 1, a) 상기 화학식 1로 표시되는 네마틱 액정 화합물 2 내지 80 중량%; 및a) 2 to 80% by weight of the nematic liquid crystal compound represented by Formula 1; And b) 하기 화학식 4, 화학식 5 및 화학식 6으로 표시되는 화합물로 이루어진 군으로부터 선택되는 적어도 1 종 이상의 액정 화합물 20 내지 98 중량%b) 20 to 98% by weight of at least one liquid crystal compound selected from the group consisting of compounds represented by the following formulas (4), (5) and (6): 를 포함하는 네마틱 액정 조성물:Nematic liquid crystal composition comprising: [화학식 4][Formula 4] [화학식 5][Formula 5] [화학식 6][Formula 6] 상기 식에서, R2및 R3는 각각 독립적으로 또는 동시에 탄소수 1 내지 15의 알킬기 또는 알콕시기이며; B는 페닐 또는 사이클로헥실이며; C는 단일결합, -CH2CH2-, 또는 -COO- 이며; X 및 Y는 각각 독립적으로 또는 동시에 수소 또는 플르오로 원자이며; Z는 수소, -OCF3또는 플루오로원자이다.Wherein R 2 and R 3 are each independently or simultaneously an alkyl or alkoxy group having 1 to 15 carbon atoms; B is phenyl or cyclohexyl; C is a single bond, -CH 2 CH 2- , or -COO-; X and Y are each independently or simultaneously hydrogen or fluoro atoms; Z is hydrogen, -OCF 3 or a fluoro atom. 제 2 항에 있어서,The method of claim 2, a) 상기 화학식 2 및 3으로 표시되는 네마틱 액정 화합물 2 내지 80 중량%; 및a) 2 to 80% by weight of the nematic liquid crystal compound represented by Formulas 2 and 3; And b) 하기 화학식 4, 화학식 5 및 화학식 6으로 표시되는 화합물로 이루어진 군으로부터 선택되는 적어도 1 종 이상의 액정 화합물 20 내지 98 중량%b) 20 to 98% by weight of at least one liquid crystal compound selected from the group consisting of compounds represented by the following formulas (4), (5) and (6): 를 포함하는 네마틱 액정 조성물:Nematic liquid crystal composition comprising: [화학식 4][Formula 4] [화학식 5][Formula 5] [화학식 6][Formula 6] 상기 식에서, R2및 R3는 각각 독립적으로 또는 동시에 탄소수 1 내지 15의 알킬기 또는 알콕시기이며; B는 페닐 또는 사이클로헥실이며; C는 단일결합, -CH2CH2-, 또는 -COO- 이며; X 및 Y는 각각 독립적으로 또는 동시에 수소 또는 플르오로 원자이며; Z는 수소, -OCF3또는 플루오로원자이다.Wherein R 2 and R 3 are each independently or simultaneously an alkyl or alkoxy group having 1 to 15 carbon atoms; B is phenyl or cyclohexyl; C is a single bond, -CH 2 CH 2- , or -COO-; X and Y are each independently or simultaneously hydrogen or fluoro atoms; Z is hydrogen, -OCF 3 or a fluoro atom. 제 2 항 또는 제 4 항에 있어서, 상기 화학식 2 및 화학식 3의 화합물의 혼합 중량비가 1 내지 80 : 1 내지 80인 네마틱 액정 조성물.The nematic liquid crystal composition according to claim 2 or 4, wherein the mixed weight ratio of the compounds of Formulas 2 and 3 is 1 to 80: 1 to 80. 제 1 항 또는 제 2 항 기재의 네마틱 액정 조성물을 포함하여 제조되는 트위스트 네마틱(TN) 디바이스 장치.A twisted nematic (TN) device device fabricated comprising the nematic liquid crystal composition of claim 1. 제 1 항 또는 제 2 항 기재의 네마틱 액정 조성물을 포함하여 제조되는 수퍼 트위스트 네마틱(STN) 디바이스 장치.A super twisted nematic (STN) device device fabricated comprising the nematic liquid crystal composition of claim 1. 제 1 항 또는 제 2 항 기재의 네마틱 액정 조성물을 포함하여 제조되는 박막트랜지스터-트위스트 네마틱(TFT-TN) 디바이스 장치.A thin film transistor-twist nematic (TFT-TN) device device made by comprising the nematic liquid crystal composition according to claim 1. 제 1 항 또는 제 2 항 기재의 네마틱 액정 조성물을 포함하여 제조되는 IPS(In plane switching) 디바이스 장치.An in plane switching (IPS) device device prepared by comprising the nematic liquid crystal composition according to claim 1. 제 1 항 또는 제 2 항 기재의 네마틱 액정 조성물을 포함하여 제조되는 AOC(Array on color filter) 또는 COA(Color filter on array) 디바이스 장치.An array on color filter (AOC) or color filter on array (COA) device device prepared by comprising the nematic liquid crystal composition of claim 1.
KR1020010065884A 2001-10-25 2001-10-25 Liquid crystal having high speed and high temperature using liquid crystal mixture of fluoroisothionate KR20030033770A (en)

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EP02724797A EP1438371A4 (en) 2001-10-25 2002-04-25 Nematic liquid crystal compound, and liquid crystal composition having high speed and high temperature comprising the same
JP2003538302A JP2005506440A (en) 2001-10-25 2002-04-25 Nematic liquid crystal compound and high-speed and high-temperature nematic liquid crystal composition containing the same
PCT/KR2002/000768 WO2003035798A1 (en) 2001-10-25 2002-04-25 Nematic liquid crystal compound, and liquid crystal composition having high speed and high temperature comprising the same
US10/493,717 US20050062018A1 (en) 2001-10-25 2002-04-25 Nematic liquid crystal compound, and liquid crystal composition having high speed and high temperature comprising the same
CNA028262379A CN1608119A (en) 2001-10-25 2002-04-25 Nematic liquid crystal compound, and liquid crystal composition having high speed and high temperature comprising the same
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