[go: up one dir, main page]

CN114806598A - A kind of negative liquid crystal composition with high contrast and its application - Google Patents

A kind of negative liquid crystal composition with high contrast and its application Download PDF

Info

Publication number
CN114806598A
CN114806598A CN202210556244.2A CN202210556244A CN114806598A CN 114806598 A CN114806598 A CN 114806598A CN 202210556244 A CN202210556244 A CN 202210556244A CN 114806598 A CN114806598 A CN 114806598A
Authority
CN
China
Prior art keywords
liquid crystal
crystal composition
carbon atoms
compound
general formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202210556244.2A
Other languages
Chinese (zh)
Inventor
李承贺
杨雪彪
刘友然
陈卯先
任婕
郭云鹏
王智成
叶宇行
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Bayi Space LCD Technology Co Ltd
Original Assignee
Beijing Bayi Space LCD Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beijing Bayi Space LCD Technology Co Ltd filed Critical Beijing Bayi Space LCD Technology Co Ltd
Priority to CN202210556244.2A priority Critical patent/CN114806598A/en
Publication of CN114806598A publication Critical patent/CN114806598A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/42Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/10Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
    • C09K19/12Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • 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)
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • 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
    • C09K19/3028Cyclohexane rings in which at least two rings are linked by a carbon chain containing carbon to carbon single bonds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/42Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
    • C09K19/44Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing compounds with benzene rings directly linked
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices 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
    • G02F1/01Devices 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 
    • G02F1/13Devices 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
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/10Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
    • C09K19/12Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
    • C09K2019/121Compounds containing phenylene-1,4-diyl (-Ph-)
    • C09K2019/124Ph-Ph-Ph-Ph
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • 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)
    • C09K2019/3004Cy-Cy
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • 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)
    • C09K2019/301Cy-Cy-Ph
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • 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
    • C09K19/3028Cyclohexane rings in which at least two rings are linked by a carbon chain containing carbon to carbon single bonds
    • C09K2019/3036Cy-C2H4-Ph
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • 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
    • C09K19/3028Cyclohexane rings in which at least two rings are linked by a carbon chain containing carbon to carbon single bonds
    • C09K2019/3037Cy-Cy-C2H4-Ph

Landscapes

  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Nonlinear Science (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

The invention relates to the field of liquid crystal materials, in particular to a negative liquid crystal composition with high contrast and application thereof. The liquid crystal composition obtained by combining the compounds shown in the general formulas I, II, III and IV can simultaneously meet the requirements of large elastic constant and low rotational viscosity, thereby realizing a liquid crystal display with high contrast.

Description

一种具有高对比度的负性液晶组合物及其应用A kind of negative liquid crystal composition with high contrast and its application

技术领域technical field

本发明涉及液晶材料领域,具体涉及一种具有高对比度的负性液晶组合物及其应用。The present invention relates to the field of liquid crystal materials, in particular to a negative liquid crystal composition with high contrast and its application.

背景技术Background technique

目前,LCD显示器作为最主流的显示器,已广泛用于各种产品中,其中IPS和FFS模式显示器因为其独有的硬屏特性以及非常宽的视角特性,目前广泛用于手机、笔记本电脑、平板电脑、电脑显示器、电视等方面。At present, LCD monitors, as the most mainstream monitors, have been widely used in various products. Among them, IPS and FFS mode monitors are widely used in mobile phones, notebook computers, tablet computers because of their unique hard screen characteristics and very wide viewing angle characteristics. Computers, computer monitors, televisions, etc.

IPS和FFS液晶平面排列导致在暗态时容易出现漏光,对比度性能方面明显劣势于VA类(MVA、PVA、UV2A、PSVA)显示器。经过研究发现,液晶分子在初始排列时,由于配向层表面存在的配向碎屑等会导致液晶分子排列紊乱从而导致暗态漏光;如何改善液晶排列紊乱成为如何提升IPS和FFS模式显示器的重要课题,通过研究发现,液晶的弹性常数增加有助于改善液晶分子的排列。The planar arrangement of IPS and FFS liquid crystals leads to light leakage easily in the dark state, and the contrast performance is obviously inferior to VA type (MVA, PVA, UV2A, PSVA) displays. After research, it has been found that when the liquid crystal molecules are initially arranged, the alignment debris on the surface of the alignment layer will cause the liquid crystal molecules to be disordered, resulting in light leakage in the dark state. Through research, it is found that the increase of the elastic constant of liquid crystal helps to improve the alignment of liquid crystal molecules.

基于此,申请人研发团队也开发出了一系列具有高对比度的负性液晶组合物,如CN113072958A,但是,随着市场的要求越来越高,仍需提供一种效果更好的具有更高对比度的负性液晶组合物。Based on this, the applicant's research and development team has also developed a series of negative liquid crystal compositions with high contrast, such as CN113072958A. However, with the increasing market requirements, it is still necessary to provide a better effect with higher Contrast negative liquid crystal compositions.

发明内容SUMMARY OF THE INVENTION

本发明的目的是提供一种具有高对比度的负性液晶组合物及其应用,所述液晶组合物具有大的弹性常数,能够改善液晶显示器对比度,同时该液晶组合物具有负的介电各向异性,用于液晶显示器中具有更高的透过率和改善液晶显示器闪烁的效果。The object of the present invention is to provide a negative liquid crystal composition with high contrast ratio and application thereof, the liquid crystal composition has a large elastic constant, can improve the contrast ratio of liquid crystal display, and at the same time, the liquid crystal composition has a negative dielectric anisotropy Anisotropy, used in liquid crystal displays to have higher transmittance and improve the effect of flickering of liquid crystal displays.

本发明提供一种具有高对比度的负性液晶组合物,包括至少一种通式I所示化合物、至少一种通式II所示化合物、至少一种通式III所示化合物以及至少一种通式IV所示化合物;The present invention provides a negative liquid crystal composition with high contrast, comprising at least one compound represented by general formula I, at least one compound represented by general formula II, at least one compound represented by general formula III, and at least one general formula a compound represented by formula IV;

Figure BDA0003654895390000011
Figure BDA0003654895390000011

Figure BDA0003654895390000021
Figure BDA0003654895390000021

其中,R1、R2各自独立地代表1-7个碳原子的烷基、1-7个碳原子的烷氧基或2-7个碳原子的烯基;Wherein, R 1 and R 2 each independently represent an alkyl group of 1-7 carbon atoms, an alkoxy group of 1-7 carbon atoms or an alkenyl group of 2-7 carbon atoms;

R3、R4各自独立地代表1-7个碳原子的烷基、1-7个碳原子的烷氧基或2-7个碳原子的烯基;R 3 and R 4 independently represent an alkyl group of 1-7 carbon atoms, an alkoxy group of 1-7 carbon atoms or an alkenyl group of 2-7 carbon atoms;

R5代表1-7个碳原子的烷基、1-7个碳原子的烷氧基或2-7个碳原子的烯基;R6代表1-7个碳原子的烷基或1-7个碳原子的烷氧基;R 5 represents an alkyl group of 1-7 carbon atoms, an alkoxy group of 1-7 carbon atoms or an alkenyl group of 2-7 carbon atoms; R 6 represents an alkyl group of 1-7 carbon atoms or an alkyl group of 1-7 carbon atoms alkoxy groups of carbon atoms;

R7、R8各自独立地代表1-7个碳原子的烷基、1-7个碳原子的烷氧基或2-7个碳原子的烯基。R 7 and R 8 each independently represent an alkyl group of 1-7 carbon atoms, an alkoxy group of 1-7 carbon atoms or an alkenyl group of 2-7 carbon atoms.

本领域公知,一般情况下,提升液晶组合物的清亮点可以实现提升弹性常数的目的,但是随着清亮点提升,液晶组合物的旋转粘度增加,从而导致液晶显示器响应时间变慢,即很难兼顾弹性常数和旋转粘度。本发明经过大量研究发现,将通式I、II、III、IV所示化合物组合得到的液晶组合物,能同时满足具有大的弹性常数和具有较低的旋转粘度,从而实现高对比度的液晶显示器。It is well known in the art that in general, the purpose of improving the elastic constant can be achieved by increasing the clearing point of the liquid crystal composition, but with the increase of the clearing point, the rotational viscosity of the liquid crystal composition increases, resulting in a slower response time of the liquid crystal display, that is, it is difficult to Take into account the elastic constant and rotational viscosity. After a lot of researches in the present invention, it is found that the liquid crystal composition obtained by combining the compounds represented by the general formulas I, II, III and IV can satisfy the requirements of having a large elastic constant and a low rotational viscosity at the same time, thereby realizing a high-contrast liquid crystal display. .

其中,所述通式I所示化合物为双环含有乙撑键的化合物,该化合物具有大的弹性常数、较低的旋转粘度和折射率;所述通式II所示化合物为三环含有乙撑键的化合物,该化合物具有大的弹性常数、较低的旋转粘度和折射率,对提高对比度有很大帮助;所述通式III所示化合物为环己烯结构的负介电各向异性化合物,该化合物具有大的弹性常数;所述通式IV所示化合物为含有双环己烷的化合物,该化合物具有好的低温溶解性能。将这四种化合物组合,比现有的其他搭配组合效果更好,能实现高对比度,同时不对其他性能产生负面影响,甚至还有正面的提升。Wherein, the compound represented by the general formula I is a bicyclic compound containing an ethylene bond, and the compound has a large elastic constant, a low rotational viscosity and a refractive index; the compound represented by the general formula II is a tricyclic compound containing an ethylene bond Bonded compound, the compound has a large elastic constant, low rotational viscosity and refractive index, which is very helpful for improving the contrast; the compound represented by the general formula III is a negative dielectric anisotropy compound of cyclohexene structure , the compound has a large elastic constant; the compound represented by the general formula IV is a compound containing bicyclohexane, and the compound has good low-temperature solubility. Combining these four compounds works better than other existing combinations, achieving high contrast without negatively impacting other properties, or even a positive boost.

根据本发明提供的具有高对比度的负性液晶组合物,According to the negative liquid crystal composition with high contrast provided by the present invention,

所述通式I所示化合物的含量为1~30wt.%,The content of the compound represented by the general formula I is 1 to 30 wt.%,

所述通式II所示化合物的含量为1~60wt.%,The content of the compound represented by the general formula II is 1-60 wt.%,

所述通式III所示化合物的含量为1~40wt.%,The content of the compound represented by the general formula III is 1-40 wt.%,

所述通式IV所示化合物的含量为1~50wt.%。The content of the compound represented by the general formula IV is 1-50 wt.%.

优选地,所述液晶组合物包括以下组分:Preferably, the liquid crystal composition includes the following components:

2~25wt.%通式I所示化合物,2 to 25 wt.% of the compound represented by the general formula I,

3~55wt.%通式II所示化合物,3 to 55 wt.% of the compound represented by the general formula II,

3~35wt.%通式III所示化合物,以及3 to 35 wt.% of the compound represented by the general formula III, and

5~45wt.%通式IV所示化合物。5-45 wt.% of the compound represented by the general formula IV.

进一步优选地,所述液晶组合物包括以下组分:Further preferably, the liquid crystal composition includes the following components:

3~20wt.%通式I所示化合物,3 to 20 wt.% of the compound represented by the general formula I,

10~50wt.%通式II所示化合物,10 to 50 wt.% of the compound represented by the general formula II,

5~30wt.%通式III所示化合物,以及5 to 30 wt.% of the compound represented by the general formula III, and

5~40wt.%通式IV所示化合物。5-40 wt.% of the compound represented by the general formula IV.

更优选地,所述液晶组合物包括以下组分:More preferably, the liquid crystal composition includes the following components:

5~15wt.%通式I所示化合物,5~15wt.% of the compound represented by the general formula I,

20~45wt.%通式II所示化合物,20 to 45 wt.% of the compound represented by the general formula II,

10~25wt.%通式III所示化合物,以及10 to 25 wt.% of the compound represented by the general formula III, and

10~35wt.%通式IV所示化合物。10-35 wt.% of the compound represented by the general formula IV.

本发明将各组分用量控制在上述配比范围内,可以确保组合物中各组分之间实现更为显著的协同效应,提高液晶组合物的各项性能。In the present invention, the dosage of each component is controlled within the above-mentioned ratio range, which can ensure a more significant synergistic effect among the components in the composition, and improve various properties of the liquid crystal composition.

根据本发明提供的具有高对比度的负性液晶组合物,所述通式I所示化合物选自IA1-IA20、IB1-IB20、IC1-IC16所代表的化合物中的一种或多种:According to the negative liquid crystal composition with high contrast provided by the present invention, the compound represented by the general formula I is selected from one or more of the compounds represented by IA1-IA20, IB1-IB20 and IC1-IC16:

Figure BDA0003654895390000031
Figure BDA0003654895390000031

Figure BDA0003654895390000041
Figure BDA0003654895390000041

Figure BDA0003654895390000051
Figure BDA0003654895390000051

Figure BDA0003654895390000061
Figure BDA0003654895390000061

优选地,所述通式I所示化合物选自IB7-IB16中的一种或多种。Preferably, the compound represented by the general formula I is selected from one or more of IB7-IB16.

根据本发明提供的具有高对比度的负性液晶组合物,所述通式II所示化合物选自IIA1-IIA20、IIB1-IIB20、IIC1-IIC14所代表的化合物中的一种或多种:According to the negative liquid crystal composition with high contrast provided by the present invention, the compound represented by the general formula II is selected from one or more of the compounds represented by IIA1-IIA20, IIB1-IIB20, and IIC1-IIC14:

Figure BDA0003654895390000062
Figure BDA0003654895390000062

Figure BDA0003654895390000071
Figure BDA0003654895390000071

Figure BDA0003654895390000081
Figure BDA0003654895390000081

优选地,所述通式II所示化合物选自IIB5-IIB18中的一种或多种。Preferably, the compound represented by the general formula II is selected from one or more of IIB5-IIB18.

根据本发明提供的具有高对比度的负性液晶组合物,所述通式III所示化合物选自IIIA1-IIIA24、IIIB1-IIIB24所代表的化合物中的一种或多种:According to the negative liquid crystal composition with high contrast provided by the present invention, the compound represented by the general formula III is selected from one or more of the compounds represented by IIIA1-IIIA24 and IIIB1-IIIB24:

Figure BDA0003654895390000082
Figure BDA0003654895390000082

Figure BDA0003654895390000091
Figure BDA0003654895390000091

优选地,所述通式III所示化合物选自IIIA13-IIIA22中的一种或多种。Preferably, the compound represented by the general formula III is selected from one or more of IIIA13-IIIA22.

根据本发明提供的具有高对比度的负性液晶组合物,所述通式IV所示化合物选自IVA1-IVA12、IVB1-IVB14所代表的化合物中的一种或多种:According to the negative liquid crystal composition with high contrast provided by the present invention, the compound represented by the general formula IV is selected from one or more of the compounds represented by IVA1-IVA12 and IVB1-IVB14:

Figure BDA0003654895390000092
Figure BDA0003654895390000092

Figure BDA0003654895390000101
Figure BDA0003654895390000101

优选地,所述通式IV所示化合物选自IVA1-IVA4、IVB6-IVB9中的一种或多种。Preferably, the compound represented by the general formula IV is selected from one or more of IVA1-IVA4 and IVB6-IVB9.

根据本发明提供的具有高对比度的负性液晶组合物,所述液晶组合物还包括一种或多种通式V所示化合物,According to the negative liquid crystal composition with high contrast provided by the present invention, the liquid crystal composition further comprises one or more compounds represented by the general formula V,

Figure BDA0003654895390000102
Figure BDA0003654895390000102

其中,R9、R10各自独立地代表1-7个碳原子的烷基或1-7个碳原子的烷氧基。Wherein, R 9 and R 10 each independently represent an alkyl group of 1-7 carbon atoms or an alkoxy group of 1-7 carbon atoms.

本发明所述通式V所示化合物为四联苯类化合物,其加入到液晶组合物中有助于配合本发明所述通式I-通式IV所示化合物,进一步提高液晶组合物的高温信赖性。The compound represented by the general formula V of the present invention is a tetrabiphenyl compound, which is added to the liquid crystal composition to help coordinate the compound represented by the general formula I to the general formula IV of the present invention, and further improve the high temperature of the liquid crystal composition. Reliability.

本发明提供的液晶组合物中,在其所有组分的质量总和为100%的情况下,通式V所示化合物在组合物中的含量在0~10%为宜,优选为0~5%,进一步优选为0~3%,更优选为0~1%。此时更有利于改善液晶显示器的响应时间。In the liquid crystal composition provided by the present invention, when the total mass of all its components is 100%, the content of the compound represented by the general formula V in the composition is preferably 0-10%, preferably 0-5% , more preferably 0 to 3%, more preferably 0 to 1%. At this time, it is more beneficial to improve the response time of the liquid crystal display.

优选地,所述通式V所示化合物选自V1-V8所代表的化合物中的一种或多种:Preferably, the compound represented by the general formula V is selected from one or more of the compounds represented by V1-V8:

Figure BDA0003654895390000103
Figure BDA0003654895390000103

Figure BDA0003654895390000111
Figure BDA0003654895390000111

在含有通式V所示化合物的情况下,为确保各组分之间的协同效应更加显著,所述液晶组合物包括以下组分:In the case of containing the compound represented by the general formula V, in order to ensure that the synergistic effect between the components is more significant, the liquid crystal composition includes the following components:

2~25wt.%通式I所示化合物,2 to 25 wt.% of the compound represented by the general formula I,

3~55wt.%通式II所示化合物,3 to 55 wt.% of the compound represented by the general formula II,

3~35wt.%通式III所示化合物,3 to 35 wt.% of the compound represented by the general formula III,

5~45wt.%通式IV所示化合物,以及5 to 45 wt.% of the compound represented by the general formula IV, and

0.01~3wt.%通式V所示化合物。0.01-3 wt.% of the compound represented by the general formula V.

更优选地,所述液晶组合物包括以下组分:More preferably, the liquid crystal composition includes the following components:

5~15wt.%通式I所示化合物,5~15wt.% of the compound represented by the general formula I,

20~45wt.%通式II所示化合物,20 to 45 wt.% of the compound represented by the general formula II,

10~25wt.%通式III所示化合物,10 to 25 wt.% of the compound represented by the general formula III,

10~35wt.%通式IV所示化合物,以及10 to 35 wt.% of the compound represented by the general formula IV, and

0.1~1wt.%通式V所示化合物。0.1 to 1 wt.% of the compound represented by the general formula V.

根据本发明提供的具有高对比度的负性液晶组合物,所述液晶组合物还包括一种或多种通式VI所示化合物,According to the negative liquid crystal composition with high contrast provided by the present invention, the liquid crystal composition further comprises one or more compounds represented by the general formula VI,

Figure BDA0003654895390000112
Figure BDA0003654895390000112

其中,R11代表1-7个碳原子的烷基、1-7个碳原子的烷氧基或2-7个碳原子的烯基;R12代表1-7个碳原子的烷基或1-7个碳原子的烷氧基。Wherein, R 11 represents an alkyl group of 1-7 carbon atoms, an alkoxy group of 1-7 carbon atoms or an alkenyl group of 2-7 carbon atoms; R 12 represents an alkyl group of 1-7 carbon atoms or 1 -Alkoxy of 7 carbon atoms.

本发明所述通式VI所示化合物为含有三环的负性化合物,该化合物具有较高的清亮点,可有效提升液晶组合物的清亮点。在液晶组合物所有组分的质量总和为100%的情况下,通式VI所示化合物在组合物中的含量在0~40%为宜,优选为5~35%,进一步优选为10~30%,更优选为15~25%。此时更有利于改善液晶显示器的工作温度区间。The compound represented by the general formula VI of the present invention is a negative compound containing a tricyclic ring, and the compound has a high clearing point, which can effectively improve the clearing point of the liquid crystal composition. When the total mass of all components of the liquid crystal composition is 100%, the content of the compound represented by the general formula VI in the composition is preferably 0-40%, preferably 5-35%, more preferably 10-30% %, more preferably 15 to 25%. At this time, it is more beneficial to improve the working temperature range of the liquid crystal display.

优选地,所述通式VI所示化合物选自VIA1-VIA24、VIB1-VIB24所代表的化合物中的一种或多种:Preferably, the compound represented by the general formula VI is selected from one or more of the compounds represented by VIA1-VIA24 and VIB1-VIB24:

Figure BDA0003654895390000121
Figure BDA0003654895390000121

Figure BDA0003654895390000131
Figure BDA0003654895390000131

在含有通式VI所示化合物的情况下,为确保各组分之间的协同效应更加显著,所述液晶组合物包括以下组分:In the case of containing the compound represented by the general formula VI, in order to ensure that the synergistic effect between the components is more significant, the liquid crystal composition includes the following components:

3~20wt.%通式I所示化合物,3 to 20 wt.% of the compound represented by the general formula I,

10~50wt.%通式II所示化合物,10 to 50 wt.% of the compound represented by the general formula II,

5~30wt.%通式III所示化合物,5-30 wt.% of the compound represented by the general formula III,

5~40wt.%通式IV所示化合物,以及5 to 40 wt.% of the compound represented by the general formula IV, and

5~35wt.%通式VI所示化合物。5-35 wt.% of the compound represented by the general formula VI.

更优选地,所述液晶组合物包括以下组分:More preferably, the liquid crystal composition includes the following components:

5~15wt.%通式I所示化合物,5~15wt.% of the compound represented by the general formula I,

20~45wt.%通式II所示化合物,20 to 45 wt.% of the compound represented by the general formula II,

10~25wt.%通式III所示化合物,10 to 25 wt.% of the compound represented by the general formula III,

10~35wt.%通式IV所示化合物,以及10 to 35 wt.% of the compound represented by the general formula IV, and

10~30wt.%通式VI所示化合物。10-30 wt.% of the compound represented by the general formula VI.

本发明所述液晶组合物的制备方法无特殊限制,可采用常规方法将两种或多种化合物混合进行生产,如通过在高温下混合不同组分并彼此溶解的方法制备,其中,将液晶组合物溶解在用于该化合物的溶剂中并混合,然后在减压下蒸馏出该溶剂;或者本发明所述液晶组合物可按照常规的方法制备,如将其中含量较小的组分在较高的温度下溶解在含量较大的主要组分中,或将各所属组分在有机溶剂中溶解,如丙酮、氯仿或甲醇等,然后将溶液混合去除溶剂后得到。The preparation method of the liquid crystal composition of the present invention is not particularly limited, and can be produced by mixing two or more compounds by conventional methods, such as by mixing different components at high temperature and dissolving each other. The compound is dissolved in the solvent used for the compound and mixed, and then the solvent is distilled off under reduced pressure; or the liquid crystal composition of the present invention can be prepared according to a conventional method, such as placing the component with a smaller content in a higher It is obtained by dissolving in the main components with a large content at a high temperature, or dissolving each component in an organic solvent, such as acetone, chloroform or methanol, etc., and then mixing the solutions to remove the solvent.

本发明还提供上述具有高对比度的负性液晶组合物在VA、IPS或FFS模式液晶显示器中的应用。The present invention also provides the application of the above negative liquid crystal composition with high contrast in VA, IPS or FFS mode liquid crystal displays.

本发明所述液晶组合物具有低旋转粘度和大的弹性常数,在优选条件下还具有良好的低温互溶性以及快的响应速度,可用于多种显示模式的快响应液晶显示,其在VA、IPS或FFS模式显示器中的使用能明显改善液晶显示器显示效果,尤其适用于IPS和FFS模式液晶显示器。The liquid crystal composition of the present invention has low rotational viscosity, large elastic constant, good low temperature mutual solubility and fast response speed under preferred conditions, and can be used for fast response liquid crystal display of various display modes. The use in IPS or FFS mode monitors can significantly improve the display effect of LCD monitors, especially for IPS and FFS mode LCD monitors.

本发明提供了一种具有高对比度的负性液晶组合物及其应用,本发明将通式I、II、III、IV所示化合物组合得到的液晶组合物,能同时满足具有大的弹性常数和具有较低的旋转粘度,从而实现高对比度的液晶显示器。The present invention provides a negative liquid crystal composition with high contrast and its application. The liquid crystal composition obtained by combining the compounds represented by the general formulas I, II, III and IV in the present invention can satisfy the requirements of having a large elastic constant and Has low rotational viscosity, enabling high contrast liquid crystal displays.

具体实施方式Detailed ways

以下实施例用于说明本发明,但不用来限制本发明的范围。The following examples are intended to illustrate the present invention, but not to limit the scope of the present invention.

除非另有说明,本发明中百分比为重量百分比;温度单位为摄氏度;△n代表光学各向异性(25℃);△ε代表介电各向异性(25℃,1000Hz);γ1代表旋转粘度(mPa.s,25℃);Cp代表液晶组合物的清亮点(℃);K11、K22、K33分别代表展曲、扭曲和弯曲弹性常数(pN,25℃)。Unless otherwise specified, the percentages in the present invention are weight percentages; the temperature is in degrees Celsius; Δn represents optical anisotropy (25°C); Δε represents dielectric anisotropy (25°C, 1000Hz); γ1 represents rotational viscosity ( mPa.s, 25°C); Cp represents the clearing point (°C) of the liquid crystal composition; K 11 , K 22 , K 33 represent the splay, twist and bending elastic constants (pN, 25° C), respectively.

以下各实施例中,液晶化合物中基团结构用表1所示代码表示。In the following examples, the group structure in the liquid crystal compound is represented by the codes shown in Table 1.

表1液晶化合物的基团结构代码Table 1 Group Structure Codes of Liquid Crystal Compounds

Figure BDA0003654895390000141
Figure BDA0003654895390000141

以如下化合物结构为例:Take the following compound structure as an example:

Figure BDA0003654895390000151
表示为:5CC2WO3
Figure BDA0003654895390000151
Represented as: 5CC2WO3

Figure BDA0003654895390000152
表示为:3CLWO2
Figure BDA0003654895390000152
Represented as: 3CLWO2

以下各实施例中,液晶组合物的制备均采用热溶解方法,包括以下步骤:用天平按重量百分比称量液晶化合物,其中称量加入顺序无特定要求,通常以液晶化合物熔点由高到低的顺序依次称量混合,在60~100℃下加热搅拌使得各组分熔解均匀,再经过滤、旋蒸,最后封装即得目标样品。In the following examples, the preparation of the liquid crystal composition adopts the thermal dissolution method, which includes the following steps: weighing the liquid crystal compound by weight percentage with a balance, wherein there is no specific requirement for the order of weighing and adding, usually the melting point of the liquid crystal compound is from high to low. Weighing and mixing in sequence, heating and stirring at 60-100°C to make each component melt evenly, then filtering, rotary steaming, and finally encapsulating to obtain the target sample.

以下各实施例中,液晶组合物中各组分的重量百分比及液晶组合物的性能参数见下述表格。In the following examples, the weight percentage of each component in the liquid crystal composition and the performance parameters of the liquid crystal composition are shown in the following table.

实施例1Example 1

表2液晶组合物中各组分的重量百分比及性能参数Table 2 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000153
Figure BDA0003654895390000153

实施例2Example 2

表3液晶组合物中各组分的重量百分比及性能参数Table 3 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000154
Figure BDA0003654895390000154

Figure BDA0003654895390000161
Figure BDA0003654895390000161

实施例3Example 3

表4液晶组合物中各组分的重量百分比及性能参数Table 4 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000162
Figure BDA0003654895390000162

实施例4Example 4

表5液晶组合物中各组分的重量百分比及性能参数The weight percent and performance parameters of each component in table 5 liquid crystal composition

Figure BDA0003654895390000163
Figure BDA0003654895390000163

Figure BDA0003654895390000171
Figure BDA0003654895390000171

实施例5Example 5

表6液晶组合物中各组分的重量百分比及性能参数Table 6 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000172
Figure BDA0003654895390000172

实施例6Example 6

表7液晶组合物中各组分的重量百分比及性能参数Table 7 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000173
Figure BDA0003654895390000173

实施例7Example 7

表8液晶组合物中各组分的重量百分比及性能参数Table 8 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000181
Figure BDA0003654895390000181

实施例8Example 8

表9液晶组合物中各组分的重量百分比及性能参数The weight percent and performance parameters of each component in the liquid crystal composition of Table 9

Figure BDA0003654895390000182
Figure BDA0003654895390000182

实施例9Example 9

表10液晶组合物中各组分的重量百分比及性能参数Table 10 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000183
Figure BDA0003654895390000183

Figure BDA0003654895390000191
Figure BDA0003654895390000191

实施例11Example 11

表12液晶组合物中各组分的重量百分比及性能参数Table 12 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000192
Figure BDA0003654895390000192

实施例12Example 12

表13液晶组合物中各组分的重量百分比及性能参数Table 13 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000193
Figure BDA0003654895390000193

Figure BDA0003654895390000201
Figure BDA0003654895390000201

实施例13Example 13

表14液晶组合物中各组分的重量百分比及性能参数Table 14 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000202
Figure BDA0003654895390000202

实施例14Example 14

表15液晶组合物中各组分的重量百分比及性能参数Table 15 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000203
Figure BDA0003654895390000203

Figure BDA0003654895390000211
Figure BDA0003654895390000211

实施例15Example 15

表16液晶组合物中各组分的重量百分比及性能参数Table 16 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000212
Figure BDA0003654895390000212

实施例16Example 16

表17液晶组合物中各组分的重量百分比及性能参数Table 17 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000213
Figure BDA0003654895390000213

Figure BDA0003654895390000221
Figure BDA0003654895390000221

实施例17Example 17

表18液晶组合物中各组分的重量百分比及性能参数Table 18 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000222
Figure BDA0003654895390000222

实施例18Example 18

表19液晶组合物中各组分的重量百分比及性能参数Table 19 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000223
Figure BDA0003654895390000223

Figure BDA0003654895390000231
Figure BDA0003654895390000231

实施例19Example 19

表20液晶组合物中各组分的重量百分比及性能参数Table 20 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000232
Figure BDA0003654895390000232

实施例20Example 20

表21液晶组合物中各组分的重量百分比及性能参数Table 21 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000233
Figure BDA0003654895390000233

Figure BDA0003654895390000241
Figure BDA0003654895390000241

实施例21Example 21

表22液晶组合物中各组分的重量百分比及性能参数Table 22 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000242
Figure BDA0003654895390000242

实施例22Example 22

表23液晶组合物中各组分的重量百分比及性能参数Table 23 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000243
Figure BDA0003654895390000243

Figure BDA0003654895390000251
Figure BDA0003654895390000251

实施例23Example 23

表24液晶组合物中各组分的重量百分比及性能参数Table 24 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000252
Figure BDA0003654895390000252

实施例24Example 24

表25液晶组合物中各组分的重量百分比及性能参数Table 25 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000253
Figure BDA0003654895390000253

Figure BDA0003654895390000261
Figure BDA0003654895390000261

实施例25Example 25

表26液晶组合物中各组分的重量百分比及性能参数Table 26 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000262
Figure BDA0003654895390000262

实施例26Example 26

表27液晶组合物中各组分的重量百分比及性能参数Table 27 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000263
Figure BDA0003654895390000263

实施例27Example 27

表28液晶组合物中各组分的重量百分比及性能参数Table 28 The weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000271
Figure BDA0003654895390000271

对比例1Comparative Example 1

表29液晶组合物中各组分的重量百分比及性能参数Table 29 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000272
Figure BDA0003654895390000272

对比例2Comparative Example 2

表30液晶组合物中各组分的重量百分比及性能参数Table 30 Weight percent and performance parameters of each component in the liquid crystal composition

Figure BDA0003654895390000273
Figure BDA0003654895390000273

Figure BDA0003654895390000281
Figure BDA0003654895390000281

实施例1、实施例27与对比例1、对比例2相比,具有更大的弹性常数,进而具有更高的对比度。Compared with Comparative Example 1 and Comparative Example 2, Example 1 and Example 27 have larger elastic constants and thus higher contrast ratios.

由以上实施例可知,本发明所提供的液晶组合物具有大的弹性常数度、高电阻率、适合的光学各向异性、良好的低温互溶性、低的旋转粘度以及优异的光稳定性和热稳定性,可降低液晶显示器的响应时间,从而解决液晶显示器响应速度慢的问题。因此,本发明所提供的液晶组合物适用于快响应的VA、IPS及FFS型TFT液晶显示装置,尤其适用于IPS及FFS液晶显示装置。It can be seen from the above examples that the liquid crystal composition provided by the present invention has large elastic constant, high resistivity, suitable optical anisotropy, good low temperature mutual solubility, low rotational viscosity and excellent light stability and thermal stability. The stability can reduce the response time of the liquid crystal display, thereby solving the problem of the slow response speed of the liquid crystal display. Therefore, the liquid crystal composition provided by the present invention is suitable for fast response VA, IPS and FFS type TFT liquid crystal display devices, especially suitable for IPS and FFS liquid crystal display devices.

虽然,上文中已经用一般性说明及具体实施方案对本发明作了详尽的描述,但在本发明基础上,可以对之作一些修改或改进,这对本领域技术人员而言是显而易见的。因此,在不偏离本发明精神的基础上所做的这些修改或改进,均属于本发明要求保护的范围。Although the present invention has been described in detail above with general description and specific embodiments, it is obvious to those skilled in the art that some modifications or improvements can be made on the basis of the present invention. Therefore, these modifications or improvements made without departing from the spirit of the present invention fall within the scope of the claimed protection of the present invention.

Claims (10)

1. A negative liquid crystal composition with high contrast is characterized by comprising at least one compound shown as a general formula I, at least one compound shown as a general formula II, at least one compound shown as a general formula III and at least one compound shown as a general formula IV;
Figure FDA0003654895380000011
wherein R is 1 、R 2 Each independently represents an alkyl group of 1 to 7 carbon atoms, an alkoxy group of 1 to 7 carbon atoms or an alkenyl group of 2 to 7 carbon atoms;
R 3 、R 4 each independently represents an alkyl group of 1 to 7 carbon atoms, an alkoxy group of 1 to 7 carbon atoms or an alkenyl group of 2 to 7 carbon atoms;
R 5 represents an alkyl group of 1 to 7 carbon atoms, an alkoxy group of 1 to 7 carbon atoms or an alkenyl group of 2 to 7 carbon atoms; r 6 Represents an alkyl group of 1 to 7 carbon atoms or an alkoxy group of 1 to 7 carbon atoms;
R 7 、R 8 each independently represents an alkyl group of 1 to 7 carbon atoms, an alkoxy group of 1 to 7 carbon atoms or an alkenyl group of 2 to 7 carbon atoms.
2. The negative liquid crystal composition with high contrast of claim 1, wherein the compound of formula I is present in an amount of 1 to 30 wt.%,
the content of the compound shown in the general formula II is 1-60 wt.%,
the content of the compound shown in the general formula III is 1-40 wt.%,
the content of the compound shown in the general formula IV is 1-50 wt.%.
3. The negative liquid crystal composition with high contrast of claim 1, wherein the compound represented by formula I is selected from one or more of the compounds represented by IA1-IA20, IB1-IB20, and IC1-IC 16:
Figure FDA0003654895380000021
Figure FDA0003654895380000031
Figure FDA0003654895380000041
preferably, the compound shown in the general formula I is selected from one or more of IB7-IB 16.
4. The negative liquid crystal composition of claim 1, wherein the compound represented by formula II is one or more compounds selected from the group consisting of IIA1-IIA20, IIB1-IIB20, IIC1-IIC 14:
Figure FDA0003654895380000042
Figure FDA0003654895380000051
Figure FDA0003654895380000061
preferably, the compound shown in the general formula II is selected from one or more of IIB5-IIB 18.
5. The negative liquid crystal composition of claim 1, wherein the compound of formula III is selected from one or more of the compounds represented by IIIA1-IIIA24, IIIB1-IIIB 24:
Figure FDA0003654895380000062
Figure FDA0003654895380000071
preferably, the compound shown in the general formula III is selected from one or more of IIIA13-IIIA 22.
6. The negative liquid crystal composition with high contrast of claim 1, wherein the compound of formula IV is selected from one or more of the compounds represented by IVA1-IVA12, IVB1-IVB 14:
Figure FDA0003654895380000081
preferably, the compound shown in the general formula IV is selected from one or more of IVA1-IVA4, IVB6-IVB 9.
7. The negative liquid crystal composition with high contrast of claim 1, wherein the liquid crystal composition further comprises one or more compounds represented by formula V,
Figure FDA0003654895380000082
wherein R is 9 、R 10 Each independently represents an alkyl group of 1 to 7 carbon atoms or an alkoxy group of 1 to 7 carbon atoms;
preferably, the compound represented by the general formula V is selected from one or more of the compounds represented by V1-V8:
Figure FDA0003654895380000091
8. the negative liquid crystal composition with high contrast of claim 1, wherein the liquid crystal composition further comprises one or more compounds represented by formula VI,
Figure FDA0003654895380000092
wherein R is 11 Represents an alkyl group of 1 to 7 carbon atoms, an alkoxy group of 1 to 7 carbon atoms or an alkenyl group of 2 to 7 carbon atoms; r 12 Represents an alkyl group of 1 to 7 carbon atoms or an alkoxy group of 1 to 7 carbon atoms;
preferably, the compound shown in the general formula VI is selected from one or more of the compounds represented by VIA1-VIA24 and VIB1-VIB 24:
Figure FDA0003654895380000093
Figure FDA0003654895380000101
9. negative liquid crystal composition with high contrast according to claim 7 or 8, characterized in that it comprises the following components:
2 to 25 wt.% of a compound of the formula I,
3 to 55 wt.% of a compound of formula II,
3 to 35 wt.% of a compound of the formula III,
5 to 45 wt.% of a compound of the formula IV, and
0.01 to 3 wt.% of a compound represented by formula V;
or,
3 to 20 wt.% of a compound of formula I,
10 to 50 wt.% of a compound of formula II,
5 to 30 wt.% of a compound of the formula III,
5 to 40 wt.% of a compound of the formula IV, and
5 to 35 wt.% of a compound of formula VI.
10. Use of a negative liquid crystal composition having a high contrast ratio according to any one of claims 1 to 9 in a VA, IPS or FFS mode liquid crystal display.
CN202210556244.2A 2022-05-20 2022-05-20 A kind of negative liquid crystal composition with high contrast and its application Pending CN114806598A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202210556244.2A CN114806598A (en) 2022-05-20 2022-05-20 A kind of negative liquid crystal composition with high contrast and its application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202210556244.2A CN114806598A (en) 2022-05-20 2022-05-20 A kind of negative liquid crystal composition with high contrast and its application

Publications (1)

Publication Number Publication Date
CN114806598A true CN114806598A (en) 2022-07-29

Family

ID=82516563

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202210556244.2A Pending CN114806598A (en) 2022-05-20 2022-05-20 A kind of negative liquid crystal composition with high contrast and its application

Country Status (1)

Country Link
CN (1) CN114806598A (en)

Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1688671A (en) * 2002-10-15 2005-10-26 默克专利股份有限公司 Photostable liquid crystalline medium
CN101161773A (en) * 2006-10-12 2008-04-16 默克专利股份有限公司 Liquid-crystalline medium
CN102482577A (en) * 2009-09-08 2012-05-30 默克专利股份有限公司 LCD Monitor
CN102834487A (en) * 2010-04-22 2012-12-19 捷恩智株式会社 Liquid crystal composition and LCD element
CN103038313A (en) * 2010-06-03 2013-04-10 捷恩智株式会社 Liquid crystal composition and liquid crystal display device
US20130105731A1 (en) * 2010-06-16 2013-05-02 Takako Ito Liquid crystal composition and liquid crystal display device
CN106462012A (en) * 2014-06-30 2017-02-22 捷恩智株式会社 Liquid crystal display element
US20170210985A1 (en) * 2014-07-29 2017-07-27 Dic Corporation Liquid-crystal display element
US20170210988A1 (en) * 2014-07-29 2017-07-27 Dic Corporation Liquid-crystal display element
US20170218270A1 (en) * 2014-07-29 2017-08-03 Dic Corporation Liquid-crystal display
CN107109232A (en) * 2014-11-12 2017-08-29 捷恩智株式会社 Liquid-crystal composition and liquid crystal display cells
CN107849457A (en) * 2015-07-23 2018-03-27 捷恩智株式会社 Liquid-crystal composition and liquid crystal display cells
CN108139629A (en) * 2015-09-25 2018-06-08 捷恩智株式会社 Liquid crystal display element
US20180187079A1 (en) * 2015-07-01 2018-07-05 Dic Corporation Composition and liquid crystal display device using the same
CN108291147A (en) * 2015-12-17 2018-07-17 捷恩智株式会社 Liquid-crystal composition and liquid crystal display element
CN108368427A (en) * 2015-12-08 2018-08-03 捷恩智株式会社 Liquid-crystal composition and liquid crystal display element
CN109844066A (en) * 2016-12-06 2019-06-04 捷恩智株式会社 Liquid crystal complex and liquid crystal light modulation element
CN111826169A (en) * 2019-04-22 2020-10-27 捷恩智株式会社 Liquid crystal composition, use thereof, and liquid crystal display element
CN111944540A (en) * 2019-05-16 2020-11-17 北京八亿时空液晶科技股份有限公司 Acetylene negative monocrystal-containing liquid crystal composition and application thereof
US20210095209A1 (en) * 2019-09-30 2021-04-01 Jiangsu Hecheng Display Technology Co., Ltd. Liquid crystal composition and photoelectric display device thereof
US20210095208A1 (en) * 2019-09-30 2021-04-01 Jiangsu Hecheng Display Technology Co., Ltd. Liquid crystal composition and photoelectric display device thereof
WO2022002997A1 (en) * 2020-07-03 2022-01-06 Merck Patent Gmbh Liquid crystal medium

Patent Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1688671A (en) * 2002-10-15 2005-10-26 默克专利股份有限公司 Photostable liquid crystalline medium
CN101161773A (en) * 2006-10-12 2008-04-16 默克专利股份有限公司 Liquid-crystalline medium
CN102482577A (en) * 2009-09-08 2012-05-30 默克专利股份有限公司 LCD Monitor
CN102834487A (en) * 2010-04-22 2012-12-19 捷恩智株式会社 Liquid crystal composition and LCD element
CN103038313A (en) * 2010-06-03 2013-04-10 捷恩智株式会社 Liquid crystal composition and liquid crystal display device
US20130105731A1 (en) * 2010-06-16 2013-05-02 Takako Ito Liquid crystal composition and liquid crystal display device
CN106462012A (en) * 2014-06-30 2017-02-22 捷恩智株式会社 Liquid crystal display element
US20170210985A1 (en) * 2014-07-29 2017-07-27 Dic Corporation Liquid-crystal display element
US20170210988A1 (en) * 2014-07-29 2017-07-27 Dic Corporation Liquid-crystal display element
US20170218270A1 (en) * 2014-07-29 2017-08-03 Dic Corporation Liquid-crystal display
CN107109232A (en) * 2014-11-12 2017-08-29 捷恩智株式会社 Liquid-crystal composition and liquid crystal display cells
US20180187079A1 (en) * 2015-07-01 2018-07-05 Dic Corporation Composition and liquid crystal display device using the same
CN107849457A (en) * 2015-07-23 2018-03-27 捷恩智株式会社 Liquid-crystal composition and liquid crystal display cells
CN108139629A (en) * 2015-09-25 2018-06-08 捷恩智株式会社 Liquid crystal display element
CN108368427A (en) * 2015-12-08 2018-08-03 捷恩智株式会社 Liquid-crystal composition and liquid crystal display element
CN108291147A (en) * 2015-12-17 2018-07-17 捷恩智株式会社 Liquid-crystal composition and liquid crystal display element
CN109844066A (en) * 2016-12-06 2019-06-04 捷恩智株式会社 Liquid crystal complex and liquid crystal light modulation element
CN111826169A (en) * 2019-04-22 2020-10-27 捷恩智株式会社 Liquid crystal composition, use thereof, and liquid crystal display element
CN111944540A (en) * 2019-05-16 2020-11-17 北京八亿时空液晶科技股份有限公司 Acetylene negative monocrystal-containing liquid crystal composition and application thereof
US20210095209A1 (en) * 2019-09-30 2021-04-01 Jiangsu Hecheng Display Technology Co., Ltd. Liquid crystal composition and photoelectric display device thereof
US20210095208A1 (en) * 2019-09-30 2021-04-01 Jiangsu Hecheng Display Technology Co., Ltd. Liquid crystal composition and photoelectric display device thereof
WO2022002997A1 (en) * 2020-07-03 2022-01-06 Merck Patent Gmbh Liquid crystal medium

Similar Documents

Publication Publication Date Title
CN104593002B (en) A kind of liquid-crystal composition with quick response
CN105670649B (en) A kind of liquid-crystal composition and its application with high transmittance
CN106883865A (en) A kind of negative dielectric anisotropy liquid crystal composition containing benzofuran and its application
WO2021134879A1 (en) Positive liquid crystal composition with high contrast
CN106883864B (en) A kind of nematic phase liquid crystal composition and its application
TWI808519B (en) A liquid crystal composition containing pyran and terphenyl and its application
CN112175629B (en) Terphenyl-containing fast response liquid crystal composition and application thereof
WO2022088915A1 (en) Liquid crystal composition comprising terphenyl and application thereof
TW202126788A (en) Negative liquid crystal composition with high contrast and application thereof
CN113072956B (en) High-contrast negative liquid crystal composition containing phenprobucol and application thereof
TWI792023B (en) Liquid crystal composition containing methoxy bridging negative liquid crystal compound and its application
CN113072955B (en) Liquid crystal composition containing methoxy bridge negative liquid crystal compound and having large elastic constant and application thereof
CN114806599A (en) A negative liquid crystal composition with large elastic constant and its application
WO2021134886A1 (en) Negative liquid crystal composition having large elastic constant and application thereof
CN115960614B (en) Positive liquid crystal composition with high contrast and application thereof
WO2021134880A1 (en) Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene structure and application thereof
CN112111283B (en) Liquid crystal composition with quick response and application thereof
CN114806598A (en) A kind of negative liquid crystal composition with high contrast and its application
CN117917459B (en) Liquid crystal composition containing dibenzothiophene compound and application thereof
WO2021134881A1 (en) Terphenyl structure-containing liquid crystal composition having large elastic constant and application thereof
CN115651669B (en) Liquid crystal composition with negative dielectric anisotropy and its application
CN116083091B (en) High-contrast negative liquid crystal composition and application thereof
TWI881186B (en) A liquid crystal composition containing terphenyl and a terminal cycloalkyl group and its application
CN112111284B (en) Pyran-containing liquid crystal composition and application thereof
CN118909641A (en) Liquid crystal composition with negative dielectric constant and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20220729