CN113072953A - Negative liquid crystal composition with large elastic constant and application thereof - Google Patents
Negative liquid crystal composition with large elastic constant and application thereof Download PDFInfo
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- CN113072953A CN113072953A CN202010006387.7A CN202010006387A CN113072953A CN 113072953 A CN113072953 A CN 113072953A CN 202010006387 A CN202010006387 A CN 202010006387A CN 113072953 A CN113072953 A CN 113072953A
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- C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
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- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
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- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
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- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3402—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom
- C09K19/3405—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom the heterocyclic ring being a five-membered ring
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- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
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- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/137—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering
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- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/12—Non-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
- C09K2019/121—Compounds containing phenylene-1,4-diyl (-Ph-)
- C09K2019/122—Ph-Ph
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- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3004—Cy-Cy
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- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
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- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
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- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
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- C09K2019/3016—Cy-Ph-Ph
Abstract
The invention relates to a liquid crystal composition, in particular to a negative liquid crystal composition with a large elastic constant and application thereof, wherein the liquid crystal composition comprises at least one of compounds represented by a general formula I, at least one of compounds represented by a general formula II, at least one of compounds represented by a general formula III and at least one of compounds represented by a general formula IV; the liquid crystal composition has large elastic constant and low rotational viscosity, and can improve contrast and realize quick response time when applied to a liquid crystal display.
Description
Technical Field
The invention relates to a liquid crystal composition, in particular to a negative liquid crystal composition with a large elastic constant and application thereof; the liquid crystal composition provided by the invention has a large elastic constant and a fast response time, and is suitable for liquid crystal displays, so that the contrast of the liquid crystal displays can be improved.
Background
Currently, LCD displays are widely used in various products as the most mainstream displays; among them, the IPS and FFS mode displays are widely used in products such as mobile phones, notebook computers, tablet computers, computer monitors, televisions, etc. because of their unique hard screen characteristics and very wide viewing angle characteristics.
IPS and FFS liquid crystal plane alignment leads to easy occurrence of light leakage in a dark state, and is significantly inferior in contrast performance to VA-type (MVA, PVA, UV2A, PSVA) displays. Research shows that when liquid crystal molecules are initially arranged, alignment debris and the like existing on the surface of an alignment layer can cause the disordered arrangement of the liquid crystal molecules so as to cause dark-state light leakage; how to improve the disorder of the liquid crystal alignment becomes a key factor of how to improve IPS and FFS mode displays, and it is found through research that an increase in the elastic constant of the liquid crystal contributes to improving the alignment of the liquid crystal molecules.
For the IPS mode and the FFS mode, positive liquid crystal can be used, and negative liquid crystal can also be used, as the negative liquid crystal molecules are arranged in the direction vertical to the electric field lines under the action of an electric field, and compared with the positive liquid crystal molecules which are arranged along the electric field lines under the action of the electric field, the negative liquid crystal molecules are used, the problems of transmittance sacrifice and flicker caused by bending the electric field under the IPS mode and the FFS mode are avoided, and further the transmittance and flicker of the liquid crystal display are improved.
The invention aims to provide a liquid crystal composition with a large elastic constant, so as to achieve the aim of improving the contrast of a liquid crystal display, and simultaneously the liquid crystal composition has negative dielectric anisotropy, has higher transmittance when being used in the liquid crystal display and has the effect of improving the flicker of the liquid crystal display.
It is known to those skilled in the art that raising the clearing point of the liquid crystal composition can achieve the purpose of raising the elastic constant, but as the clearing point is raised, the rotational viscosity of the liquid crystal composition increases, thereby causing the response time of the liquid crystal display to become slow; the liquid crystal composition provided by the invention has a large elastic constant on one hand and a low rotational viscosity on the other hand, so that a liquid crystal display with high contrast and quick response is realized.
Disclosure of Invention
The invention provides a liquid crystal composition which has a large elastic constant and low rotational viscosity, can improve the contrast ratio when being applied to a liquid crystal display and can realize quick corresponding time.
In order to achieve the purpose, the invention adopts the technical scheme that: a negative liquid crystal composition with large elastic constant comprises at least one of compounds represented by a general formula I, at least one of compounds represented by a general formula II, at least one of compounds represented by a general formula III and at least one of compounds represented by a general formula IV;
wherein, in the general formula I, R1、R2Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
in the general formula II, R3、R4Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a); n is1Represents 0 or 1; a. the1One selected from the following groups:
in the general formula III, R5、R6Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
in the general formula IV, R7、R8Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12Linear alkenyl of (A)2、A3Each independently represents trans-1, 4-cyclohexyl or 1, 4-phenylene.
The compound represented by the general formula I provided by the invention is a neutral compound containing a cyclohexene structure, the structure has a very large elastic constant, and the rotational viscosity of the compound is low, so that the elastic constant can be effectively improved when the compound is used in a liquid crystal composition.
Specifically, the compound represented by the general formula I is selected from one or more compounds represented by formulas IA to IB:
wherein R is1、R2Each independently represents C1~C7Straight chain alkyl or C2~C7A linear alkenyl group of (a);
preferably, the compound represented by formula I is selected from one or more of the compounds represented by formula IA1 to formula IB 45:
more preferably, the compound represented by the general formula I is selected from one or more of IA3, IA12, IA21, IA23, IA24, IA25, IA39, IA43, IB3, IB5, IB8, IB10, IB26, IB27, IB30 and IB 31;
particularly preferably, the compound represented by the general formula I is selected from one or more of IA3, IA21, IA23, IA24, IA25, IA39, IA43, IB3, IB5, IB8, IB10, IB26, IB27, IB30 and IB 31;
most preferably, the compound represented by formula I is selected from one or more of IA3, IA21, IA23, IA39, IB3, IB5, IB8, IB10, IB26, IB27, IB30, IB 31.
The compound represented by the general formula II provided by the invention is a tricyclic compound containing a2, 3-difluorobenzene structure, has larger negative dielectric anisotropy and high clearing point, and can effectively improve the dielectric anisotropy and the clearing point of a liquid crystal composition when being used in the liquid crystal composition.
Specifically, the compound represented by the general formula II is selected from one or more compounds represented by the formulas IIA to IIF:
wherein R is3、R4Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
preferably, the compound represented by the general formula II is one or more compounds selected from the group consisting of compounds represented by the formulas IIA 1-IIF 48:
more preferably, the compound represented by the general formula II is selected from one or more of IIA14, IIA16, IIA22, IIC14, IIC15, IID10, IID13, IID14, IID15, IID16, IID18, IIE14, IIE18, IIF13 and IIF 14.
The compound represented by the general formula III provided by the invention is a compound containing a benzofuran structure, has very large negative dielectric anisotropy and relatively large optical anisotropy, and is very effective in improving the dielectric anisotropy and the optical anisotropy of the liquid crystal composition.
Specifically, the compound represented by the general formula III is selected from one or more compounds represented by the formulas III1 to III 66:
preferably, the compound represented by the general formula III is selected from one or more of III54, III55, III56, III57 and III 63.
The compound represented by the general formula IV provided by the invention is a neutral two-ring structure compound, has very low rotational viscosity, and is very effective for reducing the rotational viscosity of a liquid crystal composition.
Specifically, the compound represented by the general formula IV is selected from one or more of the compounds represented by the formulae IVA to IVC:
wherein R is7、R8Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
preferably, the compound represented by formula IV is selected from one or more of the compounds represented by formulae IVA1 to formula IVC 24:
more preferably, the compound represented by formula IV is selected from one or more of IVA3, IVA7, IVA11, IVA12, IVA25, IVA29, IVA31, IVA37, IVB18, IVB22, IVC2, IVC4, IVC15, IVC 20;
particularly preferably, the compound represented by formula IV is selected from one or more of IVA25, IVA29, IVA37, IVB18, IVB22, IVC2, IVC4, IVC15, and IVC 20.
The liquid crystal composition provided by the invention also comprises at least one of the compounds represented by the general formulas V and/or VI:
wherein, in the general formula V, R9、R10Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a); a. the4Represents trans-1, 4-cyclohexyl or 1, 4-phenylene;
in the general formula VI, R11Represents C1~C7Straight chain alkyl or C2~C7A linear alkenyl group of (a); r12Represents C1~C7Linear alkyl or linear alkoxy of (a); l is1、L2、L3Each independently represents H or F.
Specifically, the compound represented by the general formula V is selected from one or more of compounds represented by the formulae VA to VB:
wherein R is9、R10Each independently represents C1~C7Straight chain alkyl ofAlkoxy radicals or C2~C7A linear alkenyl group of (a);
preferably, the compound represented by formula V is selected from one or more of the compounds represented by formulae VA1 to VB 38:
specifically, the compound represented by formula VI is selected from one or more of VIA or VIB:
wherein R is11Represents C1~C7Straight chain alkyl or C2~C7A linear alkenyl group of (a); r12Represents C1~C7Linear alkyl or linear alkoxy of (a);
preferably, the compound represented by formula VI is selected from one or more of the compounds represented by formula VIA1 to formula VIB 24:
in the liquid crystal composition, the general formula V and the general formula IV can be added simultaneously or alternatively.
Specifically, in order to enable the liquid crystal composition to meet different requirements, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 1-30% of a compound represented by the general formula I;
(2) 20-70% of a compound represented by the general formula II;
(3) 1-20% of a compound represented by the general formula III;
(4) 10-60% of a compound represented by the general formula IV;
(5) 0-20% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 30-66% of a compound represented by the general formula II;
(3) 2-16% of a compound represented by the general formula III;
(4) 15-55% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
more preferably, the following components are contained in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 19-47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 3-12% of a compound represented by the general formula I;
(2) 30-62% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 25-55% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-12% of a compound represented by the general formula I;
(2) 36-58% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 27 to 47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass: (1) 7-20% of a compound represented by the general formula I;
(2) 30-65% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
(5) 0 to 10% of a compound represented by the general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 7-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 19 to 46% of a compound represented by the general formula IV;
(5) 0-6% of a compound represented by general formula V and/or VI;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 45-65% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 15-47% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 45-63% of a compound represented by the general formula II;
(3) 3-11% of a compound represented by the general formula III;
(4) 19 to 43% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-55% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 25 to 50% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-55% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 27 to 47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-65% of a compound represented by the general formula II;
(3) 2-7% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-7% of a compound represented by the general formula III;
(4) 19-47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-65% of a compound represented by the general formula II;
(3) 5-15% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 5-12% of a compound represented by the general formula III;
(4) 19-47% of a compound represented by the general formula IV;
(5) 0-7% of a compound represented by general formula V and/or VI;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-65% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
preferably, the composition comprises the following components in percentage by mass:
(1) 5-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 19 to 46% of a compound represented by the general formula IV;
or, the liquid crystal composition provided by the invention comprises the following components in percentage by mass:
(1) 3-15% of a compound represented by the general formula I;
(2) 33-58% of a compound represented by the general formula II;
(3) 2-9% of a compound represented by the general formula III;
(4) 25 to 50% of a compound represented by the general formula IV;
(5) 1-10% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-12% of a compound represented by the general formula I;
(2) 36-54% of a compound represented by the general formula II;
(3) 3-7% of a compound represented by the general formula III;
(4) 30-47% of a compound represented by the general formula IV;
(5) and 5-8% of a compound represented by the general formula V and/or VI.
The liquid crystal composition provided by the invention has the advantages that the elastic constant is improved through the compound represented by the general formula I; the dielectric anisotropy and the intersolubility are improved by the compound represented by the general formula II; increasing the dielectric anisotropy and increasing the optical anisotropy by adding a compound of the formula III; reducing the rotational viscosity by adding a compound of formula IV; thereby realizing a liquid crystal composition required for a liquid crystal display having a fast response and a high contrast.
The method for producing the liquid crystal composition of the present invention is not particularly limited, and it can be produced by mixing two or more compounds by a conventional method, such as a method of mixing the different components at a high temperature and dissolving each other, wherein the liquid crystal composition is dissolved and mixed in a solvent for the compounds, and then the solvent is distilled off under reduced pressure; alternatively, the liquid crystal composition of the present invention can be prepared by a conventional method, for example, by dissolving the component having a smaller content in the main component having a larger content at a higher temperature, or by dissolving each of the components in an organic solvent, for example, acetone, chloroform or methanol, and then mixing the solutions to remove the solvent.
Detailed Description
The following examples are intended to illustrate the invention but are not intended to limit the scope of the invention.
Unless otherwise indicated, percentages in the present invention are weight percentages; the temperature units are centigrade; Δ n represents optical anisotropy (25 ℃); epsilon∥And ε⊥Respectively represent the parallel and perpendicular dielectric constants (25 ℃, 1000 Hz); Δ ε represents the dielectric anisotropy (25 ℃, 1000 Hz); γ 1 represents rotational viscosity (mpa.s, 25 ℃); cp represents the clearing point (. degree. C.) of the liquid crystal composition; k11、K22、K33Respectively representing the splay, twist and bend elastic constants (pN, 25 ℃), KavgRepresents the average elastic constant (pN, 25 ℃, (K)11+K22+K33)/3)。
In the following examples, the group structures in the liquid crystal compounds are represented by codes shown in Table 1.
Table 1: radical structure code of liquid crystal compound
Take the following compound structure as an example:
expressed as: 5OMO2
Expressed as: 3CLWO2
In the following examples, the liquid crystal composition was prepared by a thermal dissolution method, comprising the steps of: weighing the liquid crystal compound by a balance according to the weight percentage, wherein the weighing and adding sequence has no specific requirements, generally weighing and mixing the liquid crystal compound in sequence from high melting point to low melting point, heating and stirring at 60-100 ℃ to uniformly melt all the components, filtering, performing rotary evaporation, and finally packaging to obtain the target sample.
In the following examples, the weight percentages of the components in the liquid crystal composition and the performance parameters of the liquid crystal composition are shown in the following tables.
Example 1
Table 2: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 2
Table 3: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 3
Table 4: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 4
Table 5: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 5
Table 6: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 6
Table 7: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 7
Table 8: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 8
Table 9: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 9
Table 10: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 10
Table 11: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 11
Table 12: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 12
Table 13: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 13
Table 14: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 14
Table 15: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 15
Table 16: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 16
Table 17: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 17
Table 18: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 18
Table 19: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 19
Table 20: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 20
Table 21: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 21
Table 22: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 22
Table 23: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 23
Table 24: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 24
Table 25: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 25
Table 26: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 26
Table 27: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 27
Table 28: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 28
Table 29: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 29
Table 30: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 30
Table 31: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 31
Table 32: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 32
Table 33: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 33
Table 34: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 34
Table 35: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 35
Table 36: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 36
Table 37: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 37
Table 38: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 38
Table 39: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 39
Table 40: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 40
Table 41: the weight percentage and performance parameters of each component in the liquid crystal composition
EXAMPLE 41
Table 42: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 42
Table 43: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 43
Table 44: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 44
Table 45: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 45
Table 46: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 46
Table 47: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 47
Table 48: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 48
Table 49: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 49
Table 50: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 50
Table 51: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 51
Table 52: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 52
Table 53: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 53
Table 54: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 54
Table 55: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 55
Table 56: the weight percentage and performance parameters of each component in the liquid crystal composition
Example 56
Table 57: the weight percentage and performance parameters of each component in the liquid crystal composition
Comparative example 1
Table 58: the weight percentage and performance parameters of each component in the liquid crystal composition
The liquid crystal compositions obtained in example 1 and comparative example 1 were compared together for each of their performance parameter values, see Table 59.
Table 59: comparison of Performance parameters of liquid Crystal compositions
Item | △n | △ε | Cp | γ1 | K11 | K22 | K33 | Kavg |
Example 1 | 0.108 | -4.0 | 80 | 85 | 15.2 | 7.6 | 16.6 | 13.1 |
Comparative example 1 | 0.106 | -3.6 | 80 | 88 | 13.8 | 6.9 | 15.3 | 12.0 |
By comparison, it can be seen that: compared with comparative example 1, the liquid crystal composition provided by example 1 has a larger elastic constant, and compared with comparative example 1, the elastic constant of example 1 is improved by about 10%, namely, the contrast ratio can be increased by about 10% when the liquid crystal composition is used in a liquid crystal display.
As can be seen from the above examples, the liquid crystal composition provided by the present invention has a large elastic constant, and can effectively improve the contrast of the liquid crystal display when used in IPS and FFS mode displays. Therefore, the liquid crystal composition provided by the invention is suitable for an IPS or FFS type TFT liquid crystal display device, can obviously improve the contrast of the liquid crystal display, and can improve the contrast characteristic of the IPS or FFS mode liquid crystal display.
Although the invention has been described in detail hereinabove by way of general description, specific embodiments and experiments, it will be apparent to those skilled in the art that many modifications and improvements can be made thereto based on the invention. Accordingly, such modifications and improvements are intended to be within the scope of the invention as claimed.
Claims (10)
1. A negative liquid crystal composition with large elastic constant is characterized by comprising at least one of compounds represented by a general formula I, at least one of compounds represented by a general formula II, at least one of compounds represented by a general formula III and at least one of compounds represented by a general formula IV;
wherein, in the general formula I, R1、R2Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
in the general formula II, R3、R4Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a); n is1Represents 0 or 1; a. the1One selected from the following groups:
in the general formula III, R5、R6Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
in the general formula IV, R7、R8Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12Linear alkenyl of (A)2、A3Each independently represents trans-1, 4-cyclohexyl or 1, 4-phenylene.
2. The liquid crystal composition of claim 1, wherein the compound represented by formula I is selected from one or more compounds represented by formulae IA to IB:
wherein R is1、R2Each independently represents C1~C7Straight chain alkyl or C2~C7A linear alkenyl group of (a);
preferably, the compound represented by formula I is selected from one or more of the compounds represented by formula IA1 to formula IB 45:
more preferably, the compound represented by the general formula I is selected from one or more of IA3, IA12, IA21, IA23, IA24, IA25, IA39, IA43, IB3, IB5, IB8, IB10, IB26, IB27, IB30 and IB 31;
particularly preferably, the compound represented by the general formula I is selected from one or more of IA3, IA21, IA23, IA24, IA25, IA39, IA43, IB3, IB5, IB8, IB10, IB26, IB27, IB30 and IB 31;
most preferably, the compound represented by formula I is selected from one or more of IA3, IA21, IA23, IA39, IB3, IB5, IB8, IB10, IB26, IB27, IB30, IB 31.
3. The liquid crystal composition of claim 1 or 2, wherein the compound represented by formula II is selected from one or more compounds represented by formulae IIA to IIF:
wherein R is3、R4Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
preferably, the compound represented by the general formula II is one or more compounds selected from the group consisting of compounds represented by the formulas IIA 1-IIF 48:
more preferably, the compound represented by the general formula II is selected from one or more of IIA14, IIA16, IIA22, IIC14, IIC15, IID10, IID13, IID14, IID15, IID16, IID18, IIE14, IIE18, IIF13 and IIF 14.
4. The liquid crystal composition according to any one of claims 1 to 3, wherein the compound represented by the general formula III is one or more compounds selected from the group consisting of compounds represented by the formulae III1 to III 66:
preferably, the compound represented by the general formula III is selected from one or more of III54, III55, III56, III57 and III 63.
5. The liquid crystal composition according to any one of claims 1 to 4, wherein the compound represented by the general formula IV is one or more compounds selected from the group consisting of compounds represented by formulas IVA to IVC:
wherein R is7、R8Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a);
preferably, the compound represented by formula IV is selected from one or more of the compounds represented by formulae IVA1 to formula IVC 24:
more preferably, the compound represented by formula IV is selected from one or more of IVA3, IVA7, IVA11, IVA12, IVA25, IVA29, IVA31, IVA37, IVB18, IVB22, IVC2, IVC4, IVC15, IVC 20;
particularly preferably, the compound represented by formula IV is selected from one or more of IVA25, IVA29, IVA37, IVB18, IVB22, IVC2, IVC4, IVC15, and IVC 20.
6. The liquid crystal composition according to any one of claims 1 to 5, further comprising at least one of compounds represented by general formulae V and/or VI:
wherein, in the general formula V, R9、R10Each independently represents C1~C12Linear alkyl, linear alkoxy or C2~C12A linear alkenyl group of (a); a. the4Represents trans-1, 4-cyclohexyl or 1, 4-phenylene;
in the general formula VI, R11Represents C1~C7Straight chain alkyl or C2~C7A linear alkenyl group of (a); r12Represents C1~C7Linear alkyl or linear alkoxy of (a); l is1、L2、L3Each independently represents H or F.
7. The liquid crystal composition of claim 6, wherein the compound represented by formula V is one or more compounds selected from the group consisting of compounds represented by formulas VA to VB:
wherein R is9、R10Each independently represents C1~C7Linear alkyl, linear alkoxy or C2~C7A linear alkenyl group of (a);
preferably, the compound represented by formula V is selected from one or more of the compounds represented by formulae VA1 to VB 38:
8. the liquid crystal composition of claim 6 or 7, wherein the compound represented by formula VI is selected from one or more of VIA or VIB:
wherein R is11Represents C1~C7Straight chain alkyl or C2~C7A linear alkenyl group of (a); r12Represents C1~C7Linear alkyl or linear alkoxy of (a);
preferably, the compound represented by formula VI is selected from one or more of the compounds represented by formula VIA1 to formula VIB 24:
9. the liquid crystal composition according to any one of claims 1 to 8, wherein the liquid crystal composition comprises the following components in percentage by mass:
(1) 1-30% of a compound represented by the general formula I;
(2) 20-70% of a compound represented by the general formula II;
(3) 1-20% of a compound represented by the general formula III;
(4) 10-60% of a compound represented by the general formula IV;
(5) 0-20% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 30-66% of a compound represented by the general formula II;
(3) 2-16% of a compound represented by the general formula III;
(4) 15-55% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
more preferably, the following components are contained in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 19-47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 3-12% of a compound represented by the general formula I;
(2) 30-62% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 25-55% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-12% of a compound represented by the general formula I;
(2) 36-58% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 27 to 47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 7-20% of a compound represented by the general formula I;
(2) 30-65% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
(5) 0 to 10% of a compound represented by the general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 7-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 19 to 46% of a compound represented by the general formula IV;
(5) 0-6% of a compound represented by general formula V and/or VI;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 45-65% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 15-47% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 45-63% of a compound represented by the general formula II;
(3) 3-11% of a compound represented by the general formula III;
(4) 19 to 43% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-55% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 25 to 50% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-55% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 27 to 47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-65% of a compound represented by the general formula II;
(3) 2-7% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-7% of a compound represented by the general formula III;
(4) 19-47% of a compound represented by the general formula IV;
(5) 0-8% of a compound represented by general formula V and/or VI;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-65% of a compound represented by the general formula II;
(3) 5-15% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
(5) 0-12% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 5-12% of a compound represented by the general formula III;
(4) 19-47% of a compound represented by the general formula IV;
(5) 0-7% of a compound represented by general formula V and/or VI;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 3-20% of a compound represented by the general formula I;
(2) 33-65% of a compound represented by the general formula II;
(3) 2-15% of a compound represented by the general formula III;
(4) 15-50% of a compound represented by the general formula IV;
preferably, the composition comprises the following components in percentage by mass:
(1) 5-16% of a compound represented by the general formula I;
(2) 36-63% of a compound represented by the general formula II;
(3) 3-12% of a compound represented by the general formula III;
(4) 19 to 46% of a compound represented by the general formula IV;
or the liquid crystal composition comprises the following components in percentage by mass:
(1) 3-15% of a compound represented by the general formula I;
(2) 33-58% of a compound represented by the general formula II;
(3) 2-9% of a compound represented by the general formula III;
(4) 25 to 50% of a compound represented by the general formula IV;
(5) 1-10% of a compound represented by general formula V and/or VI;
preferably, the composition comprises the following components in percentage by mass:
(1) 4-12% of a compound represented by the general formula I;
(2) 36-54% of a compound represented by the general formula II;
(3) 3-7% of a compound represented by the general formula III;
(4) 30-47% of a compound represented by the general formula IV;
(5) and 5-8% of a compound represented by the general formula V and/or VI.
10. Use of the liquid crystal composition according to any one of claims 1 to 9 in a liquid crystal display which is an IPS or FFS mode display.
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CN202010006387.7A CN113072953A (en) | 2020-01-03 | 2020-01-03 | Negative liquid crystal composition with large elastic constant and application thereof |
PCT/CN2020/077022 WO2021134886A1 (en) | 2020-01-03 | 2020-02-27 | Negative liquid crystal composition having large elastic constant and application thereof |
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CN114806599A (en) * | 2022-05-20 | 2022-07-29 | 北京八亿时空液晶科技股份有限公司 | Negative liquid crystal composition with large elastic constant and application thereof |
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WO2016115928A1 (en) * | 2015-01-21 | 2016-07-28 | 北京八亿时空液晶科技股份有限公司 | Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene liquid crystal compound and application thereof |
WO2016171064A1 (en) * | 2015-04-24 | 2016-10-27 | Dic株式会社 | Nematic liquid crystal composition, and liquid crystal display element manufactured using same |
CN109837096A (en) * | 2017-11-24 | 2019-06-04 | 默克专利股份有限公司 | Liquid crystal media |
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US5064565A (en) * | 1989-07-26 | 1991-11-12 | Chisso Corporation | Cyclohexenylethane compound |
EP3095834B9 (en) * | 2015-05-21 | 2019-09-04 | Merck Patent GmbH | Liquid-crystalline medium and liquid-crystal display comprising the same |
DE102016009412A1 (en) * | 2015-08-05 | 2017-02-09 | Merck Patent Gmbh | Liquid crystalline medium |
EP3299438B1 (en) * | 2016-09-23 | 2020-01-15 | Merck Patent GmbH | Liquid-crystalline medium and liquid-crystal display comprising the same |
WO2018193859A1 (en) * | 2017-04-17 | 2018-10-25 | Dic株式会社 | Liquid crystal display device |
EP3421570B1 (en) * | 2017-06-30 | 2020-11-11 | Merck Patent GmbH | Liquid-crystalline medium and liquid-crystal display comprising the same |
EP3697868A1 (en) * | 2017-10-18 | 2020-08-26 | Merck Patent GmbH | Liquid-crystalline medium and liquid-crystal display comprising the same |
CN109943347A (en) * | 2017-12-20 | 2019-06-28 | 石家庄诚志永华显示材料有限公司 | Liquid-crystal composition and liquid crystal display element |
CN109880637B (en) * | 2019-03-29 | 2023-08-08 | 石家庄诚志永华显示材料有限公司 | Liquid crystal composition, liquid crystal display element and liquid crystal display |
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2020
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WO2016115928A1 (en) * | 2015-01-21 | 2016-07-28 | 北京八亿时空液晶科技股份有限公司 | Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene liquid crystal compound and application thereof |
WO2016171064A1 (en) * | 2015-04-24 | 2016-10-27 | Dic株式会社 | Nematic liquid crystal composition, and liquid crystal display element manufactured using same |
CN109837096A (en) * | 2017-11-24 | 2019-06-04 | 默克专利股份有限公司 | Liquid crystal media |
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CN114806599A (en) * | 2022-05-20 | 2022-07-29 | 北京八亿时空液晶科技股份有限公司 | Negative liquid crystal composition with large elastic constant and application thereof |
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