CN111117649B - Liquid crystal composition and display device thereof - Google Patents

Liquid crystal composition and display device thereof Download PDF

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CN111117649B
CN111117649B CN201811272205.XA CN201811272205A CN111117649B CN 111117649 B CN111117649 B CN 111117649B CN 201811272205 A CN201811272205 A CN 201811272205A CN 111117649 B CN111117649 B CN 111117649B
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CN111117649A (en
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贺笛
徐海彬
刘云云
张文琦
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Jiangsu Hecheng Display Technology Co Ltd
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
    • C09K19/44—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing compounds with benzene rings directly linked
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
    • C09K19/46—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing esters
    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL 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
    • G02F1/00—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
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods

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Abstract

The present invention provides a liquid crystal composition comprising: at least one compound of the general formula I; at least one compound of the general formula II; at least one compound of the general formula III; and at least one compound of the general formula M. The invention also provides a display device comprising the liquid crystal composition. The liquid crystal composition provided by the invention has high dielectric anisotropy, appropriately high optical anisotropy, appropriately high clearing point, high transmittance, good low-temperature stability and larger KaveSo that the liquid crystal display device comprising the liquid crystal composition has higher contrast ratio, relatively less light scattering and good display effect.

Description

Liquid crystal composition and display device thereof
Technical Field
The invention relates to the field of liquid crystal materials, in particular to a liquid crystal composition and a display device thereof.
Background
The liquid crystal material is a mixture of organic rod-shaped small molecular compounds which have liquid fluidity and crystal anisotropy at a certain temperature. Liquid crystal display devices operate by utilizing optical anisotropy and dielectric anisotropy of liquid crystal materials themselves, and are currently widely used. The liquid crystal display device is classified into: phase Change (PC), Twisted Nematic (TN), Super Twisted Nematic (STN), Dynamic Scattering (DS), Ferroelectric (FLC), guest-host (GH), Electrically Controlled Birefringence (ECB), Optically Compensated Bend (OCB), in-plane switching (IPS), Vertical Alignment (VA), Fringe Field Switching (FFS), field-induced photo-reactive alignment (FPA), and the like.
Liquid Crystal Displays (LCDs) have been rapidly developed due to their small size, light weight, low power consumption and excellent Display quality, and are widely used particularly in portable electronic information products. As the size of a liquid crystal screen for a portable computer, an office application, a video application increases, in order to enable the liquid crystal display to be used for a large screen display and eventually replace a Cathode Ray Tube (CRT), there are still some problems to be solved, such as improvement of viewing angle characteristics, improvement of response speed, increase of contrast, improvement of transmittance, and the like. The narrow viewing angle of the LCD means that the contrast ratio is significantly reduced when viewed from a direction perpendicular to the normal of the liquid crystal cell, and the phenomenon of gray scale and color inversion occurs when the viewing angle is large, which seriously affects the display quality of the LCD.
The viewing angle problem of LCDs is determined by the operating principle of the liquid crystal material. The liquid crystal molecules themselves are rod-shaped, and different molecular alignment modes correspond to different optical anisotropies. The smaller the included angle between incident light and liquid crystal molecules is, the smaller the birefringence is; conversely, the greater the birefringence. The included angles between the light rays entering the liquid crystal box at different angles from the normal direction of the display screen and the director of the liquid crystal molecules are different, so that the effective optical path difference delta n x d is different at different viewing angles. However, the optical path difference of the liquid crystal cell is designed according to the normal direction perpendicular to the liquid crystal cell, and for the light rays with oblique incidence, the minimum transmittance increases with the increase of the included angle, the contrast ratio decreases, and when the included angle is large enough, the contrast ratio even reverses.
At present, many methods for solving the viewing angle problem have been proposed, such as: an Optically Compensated Bend (OCB) mode, an in-plane switching (IPS) mode, a Fringe Field Switching (FFS) mode, and a multi-domain vertical alignment (MVA) mode. They all have their own advantages and disadvantages: the MVA mode has high contrast and fast response characteristics, but it requires one biaxial compensation film and two elliptical polarizers, and thus is high in cost; the OCB mode is difficult to maintain stable control with ac voltage, the transmittance of R, G, B three monochromatic lights is different, and in the absence of field, the molecules in the liquid crystal cell are aligned in the direction parallel to the substrate, and in order to achieve bend alignment, a voltage is applied to the cell for several seconds for presetting, and then the alignment can be maintained at a lower voltage, which is inconvenient to use; the IPS mode requires only a linear polarizer and does not require a compensation film, but its response speed is too slow to display a fast moving picture. Since the IPS mode and the FFS mode are simple to manufacture and have a wide viewing angle, they are the most attractive approaches capable of improving viewing angle characteristics and realizing large-area display.
In the early 70 s of the last century, experimental studies have been conducted on the basic electro-optical characteristics of the IPS mode of nematic liquid crystals, both uniformly aligned and twisted, characterized in that a pair of electrodes is made on the same substrate, while the other substrate has no electrode, and the alignment of the liquid crystal molecules is controlled by a transverse electric field applied between the pair of electrodes, and thus this mode can also be called lateral field mode. In the IPS mode, nematic liquid crystal molecules are uniformly arranged in parallel between two substrates, and two polarizing plates are orthogonally arranged. In the IPS mode, when no electric field is applied, incident light is blocked by two orthogonal polarizing plates to be in a dark state, and when an electric field is applied, liquid crystal molecules rotate to cause retardation, so that light leaks from the two orthogonal polarizing plates.
With the wide application of TFT-type LCDs, the performance requirements of TFT-type LCDs are continuously increasing, and high display image quality requires faster response speed, lower power consumption, and higher low-temperature reliability, and in addition, higher contrast and transmittance are required, especially for IPS-type liquid crystal display modes. This means that liquid crystal materials are required to have higher contrast and transmittance, higher elastic constant, higher dielectric constant and low temperature reliability, and improvement of these properties is required.
Transmittance equation Transmitance (Transmittance, T). alpha.. DELTA.. epsilon./E.epsilon.. according to IPS mode⊥(". varies" indicates an "inverse proportion" relationship, ε⊥Showing a dielectric constant in a direction perpendicular to the molecular axis), it is possible to try to reduce Δ ∈ of the liquid crystal medium in order to increase the transmittance of the liquid crystal material, but generally, the adjustment range of the driving voltage of the same product is limited. In addition, the liquid crystal molecules will tilt in the Z-axis direction under the action of the vertical component of the fringe electric field, so that the optical anisotropy delta n of the liquid crystal molecules changes according to the formula
Figure RE-GDA0001881743840000021
(where χ is the angle between the optic axis of the liquid crystal layer and the optic axis of the polarizer, Δ n is the optical anisotropy, d is the cell gap, λ is the wavelength), it is known that the effective Δ n × d affects T, and if the transmittance of the positive liquid crystal material is to be improved, it can be considered to increase Δ n × d, but the retardation design of each product is fixed.
On the other hand, based on the conventional IPS-LCD light leakage test, those skilled in the art find that the main factors causing the light leakage problem of the liquid crystal display device are: light scattering (LC scattering), rubbing uniformity (rubbing uniformity), color filter light leakage (CF/TFT scattering), and polarization ability (polarization ability), wherein light scattering accounts for 63% of the factors affecting light leakage.
According to the following relationship:
Figure RE-GDA0001881743840000022
in order to improve the light scattering of the liquid crystal material, it is necessary to increase the average elastic constant Kave(wherein,
Figure RE-GDA0001881743840000031
) To improve light scattering; at the increase of KaveIn the case of (2), light leakage of the liquid crystal material can be reduced.
Further, the Contrast (CR) and the luminance (L) are related as follows:
CR＝L255/L0×100％，
wherein L is255Is at on-state brightness, L0Is off state brightness. It can be seen that what significantly affects CR should be L0A change in (c). In the off state, L0The smaller the light scattering (LC scattering), L, is, independent of the dielectric of the liquid crystal molecules, in relation to the light scattering (LC scattering) of the liquid crystal material itself0The smaller the Contrast Ratio (CR) will be, the more significantly the contrast ratio will be.
In view of the above, the conventional method for increasing the transmittance of the liquid crystal material can be considered from the following two aspects: (1) by increasing epsilon while keeping constant the dielectric anisotropy Delta epsilon of the liquid crystal composition⊥The transmittance can be effectively improved; (2) increase the average elastic constant K of the liquid crystal compositionaveThe value of (b) makes the degree of order of the liquid crystal molecules better and the light leakage less, thereby improving the transmittance. In view of some defects of the prior liquid crystal composition, the invention provides a liquid crystal composition with good performance, in particular a liquid crystal composition with characteristics of high transmittance, high average elastic constant, good low-temperature stability and the like.
Disclosure of Invention
The purpose of the invention is as follows: the invention aims to provide a transparent film having high dielectric anisotropy, suitably high optical anisotropy, suitably high clearing point, high transmittance, good low temperature stability, and large KaveThe liquid crystal composition of (1). The invention also aims to provide a liquid crystal display device comprising the liquid crystal composition.
The technical scheme of the invention is as follows:
in order to achieve the above object, the present invention provides a liquid crystal composition comprising:
at least one compound of the general formula I
Figure RE-GDA0001881743840000032
At least one compound of the general formula II
Figure RE-GDA0001881743840000033
At least one compound of the formula III
Figure RE-GDA0001881743840000034
And
at least one compound of the formula M
Figure RE-GDA0001881743840000041
Wherein,
R1and RA2Each independently represents a linear or branched alkyl group having 1 to 12 carbon atoms,
Figure RE-GDA0001881743840000042
Figure RE-GDA0001881743840000043
1 or non-adjacent 2 or more-CH in the linear or branched alkyl containing 1 to 12 carbon atoms2-said linear or branched alkyl containing 1 to 12 carbon atoms, which may be independently replaced by-C ═ C-, -C ≡ C-, -O-, -CO-O-or-O-CO-, respectively,
Figure RE-GDA0001881743840000044
Each of one or more-H may be independently substituted with-F or-Cl;
R2represents a linear or branched alkyl group having 1 to 12 carbon atoms, a linear or branched alkenyl group having 2 to 12 carbon atoms,
Figure RE-GDA0001881743840000045
In the linear or branched alkyl group having 1 to 12 carbon atoms1 or non-adjacent 2 or more-CH2-each independently can be replaced by-C.ident.C-, -O-, -CO-O-or-O-CO-and said linear or branched alkyl group containing 1 to 12 carbon atoms, linear or branched alkenyl group containing 2 to 12 carbon atoms,
Figure RE-GDA0001881743840000046
Each of one or more-H may be independently substituted with-F or-Cl;
RM1and RM2Each independently represents-H, a linear or branched alkyl group having 1 to 12 carbon atoms, a linear or branched alkenyl group having 2 to 12 carbon atoms,
Figure RE-GDA0001881743840000047
1 or non-adjacent 2 or more-CH in the linear or branched alkyl containing 1 to 12 carbon atoms2-may be independently replaced by-C.ident.C-, -O-, -CO-O-or-O-CO-;
ring (C)
Figure RE-GDA0001881743840000048
Ring (C)
Figure RE-GDA0001881743840000049
Ring (C)
Figure RE-GDA00018817438400000410
And ring
Figure RE-GDA00018817438400000411
Each independently represent
Figure RE-GDA00018817438400000412
Wherein,
Figure RE-GDA00018817438400000413
one or more-CH2-may be replaced by-O-, one or more of the ring single bonds may be replaced by double bonds,
Figure RE-GDA00018817438400000414
may be substituted by-CN, -F or-Cl, and one or more rings may be substituted by-CH ═ by-N;
ring (C)
Figure RE-GDA00018817438400000415
Ring (C)
Figure RE-GDA00018817438400000416
And ring
Figure RE-GDA00018817438400000417
Each independently represent
Figure RE-GDA00018817438400000418
Figure RE-GDA00018817438400000419
Wherein
Figure RE-GDA00018817438400000420
One or more-CH of2-can be replaced by-O-,
Figure RE-GDA00018817438400000421
at most one-H in (a) may be substituted by halogen;
Z1、Z2and Z3Each independently represents a single bond, -CH2CH2-、-CF2CF2-、-CF2O-、-OCF2-、-CO-O-、 -O-CO-、-O-CO-O-、-CH＝CH-、-CF＝CF-、-CH2O-or-OCH2-；
ZA21And ZA22Each independently represents a single bond, -CH2CH2-、-CF2CF2-、-CO-O-、-O-CO-、-O-CO-O-、 -CH＝CH-、-CF＝CF-、-CH2O-or-OCH2-；
ZM1And ZM2Each independently represents a single bond, -CO-O-, -O-CO-, -CH2O-、-OCH2-、-CH＝CH-、 -C≡C-、-CH2CH2-or- (CH)2)4-；
L1、L2、L3、L4、LA21、LA22、LA23And LA24Each independently represents-H, an alkyl group having 1 to 3 carbon atoms, or a halogen;
x represents halogen, haloalkyl or haloalkoxy having 1 to 5 carbon atoms, haloalkenyl or haloalkenyloxy having 2 to 5 carbon atoms;
XA2represents halogen, haloalkyl or haloalkoxy having 1 to 5 carbon atoms, haloalkenyl or haloalkenyloxy having 2 to 5 carbon atoms;
X21represents halogen, haloalkyl or haloalkoxy having 1 to 5 carbon atoms, haloalkenyl or haloalkenyloxy having 2 to 5 carbon atoms;
X22and X23Each independently represents-H, halogen, haloalkyl or haloalkoxy having 1 to 3 carbon atoms, haloalkenyl or haloalkenyloxy having 2 to 3 carbon atoms, wherein X22And X23Only one of them represents H;
n1 and n2 each independently represent 0, 1 or 2, and 0. ltoreq. n1+ n 2. ltoreq.3, and when n 1. ltoreq.2, the ring
Figure RE-GDA0001881743840000051
May be the same or different, Z1Which may be the same or different, when n2 is 2, the ring
Figure RE-GDA0001881743840000052
May be the same or different, Z2May be the same or different;
nA2represents 0, 1, 2 or 3, and when nA2When 2 or 3, ring
Figure RE-GDA0001881743840000053
May be the same or different, ZA21May be the same or different;
nM1represents 0, 1, 2 or 3, and when nM1When 2 or 3, ring
Figure RE-GDA0001881743840000054
May be the same or different, ZM2May be the same or different;
when Z isA21And ZA22Represents a single bond, nA2Denotes 1, ring
Figure RE-GDA0001881743840000055
To represent
Figure RE-GDA0001881743840000056
Ring (C)
Figure RE-GDA0001881743840000057
Represents one or more of-H which may be substituted by-F or-Cl
Figure RE-GDA0001881743840000058
When L isA21、LA22、LA23And LA24At least one is not-H;
when Z is1、Z2And Z3Each independently represents a single bond, -CH2CH2-、-CF2CF2-、-CO-O-、-O-CO-、-O-CO-O-、 -CH＝CH-、-CF＝CF-、-CH2O-or-OCH2-when 2. ltoreq. n1+ n 2. ltoreq.3; and is
When the ring
Figure RE-GDA0001881743840000059
And ring
Figure RE-GDA00018817438400000510
Is one of
Figure RE-GDA00018817438400000511
When n is greater than nA2Represents 1.
In some embodiments of the invention, the dielectric anisotropy of the compounds of formula I and the compounds of formula II are both positive.
In some embodiments of the invention, the absolute value of the dielectric anisotropy of the compound of formula II is not less than 4.
In some embodiments of the invention, the absolute value of the dielectric anisotropy of the compound of formula M is not more than 3; preferably, the absolute value of the dielectric anisotropy of the compound of formula M does not exceed 2.
In some embodiments of the present invention, the content of the compound of formula i is desirably adjusted according to the required properties of solubility at low temperature, transition temperature, electrical reliability, transmittance, contrast, birefringence, process adaptability, dropping marks, burn-in, dielectric anisotropy, and the like.
The compounds of the general formula I preferably represent the liquid crystal compositions according to the invention in a weight ratio: the lower limit of the weight percentage of the compound of formula i in the liquid crystal composition of the present invention is preferably 0.1%, 0.5%, 1%, 2%, 3%, 4%, 5%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 20%, 30% or 40% relative to the total weight of the liquid crystal composition of the present invention; the upper limit of the weight percentage of the compound of formula I in the liquid crystal composition of the present invention is preferably 60%, 55%, 50%, 45%, 40%, 35%, 30%, 28%, 27%, 26%, 25.5%, 25%, 24.5%, 24%, 22%, 20%, 18%, 16% or 15% relative to the total weight of the liquid crystal composition of the present invention.
In some embodiments of the invention, the compound of formula I is present in an amount of 0.1% to 60% by weight of the liquid crystal composition.
In some embodiments of the invention, in the compounds of formula i, when n1 ═ 0, Z is2And Z3Is not a single bond; when n1 equals 1 and n2 equals 1, Z1、Z2And Z3Each independently represents a single bond, -CH2CH2-、-CF2CF2-、 -CO-O-、-O-CO-、-O-CO-O-、-CH＝CH-、-CF＝CF-、-CH2O-or-OCH2-; when n1 is 1 and n2 is 0, Z is1And Z3At least one of which is not a single bond.
In some embodiments of the invention, inIn the compounds of the formula I, R1Preferably a linear or branched alkyl or alkoxy group having 1 to 8 carbon atoms, a linear or branched alkenyl or alkenyloxy group having 2 to 8 carbon atoms; further preferred is a linear or branched alkyl group or alkoxy group having 1 to 5 carbon atoms, a linear or branched alkenyl group or alkenyloxy group having 2 to 5 carbon atoms.
In some embodiments of the invention, the ring
Figure RE-GDA0001881743840000061
And ring
Figure RE-GDA0001881743840000062
Each independently represent
Figure RE-GDA0001881743840000063
In some embodiments of the invention, L1、L2、L3And L4Each independently represents-H, -CH3-F or-Cl.
In some embodiments of the invention, the compound of formula i is selected from the group consisting of:
Figure RE-GDA0001881743840000071
Figure RE-GDA0001881743840000081
and
Figure RE-GDA0001881743840000082
wherein,
L5、L6and L7Each independently represents-H or-F;
Rxand RyEach independently represents-CH2-or-O-; and is
n1 represents 0 or 1.
In some embodiments of the present invention, the liquid crystal compositions of the present invention preferably comprise at least one compound of formula I; more preferably at least one compound of the general formulae I-1 to I-9, I-11; further preferred are compounds of 2 to 10 kinds of the general formulae I-1 to I-9 and I-11.
In some embodiments of the present invention, the liquid crystal compositions of the present invention preferably comprise at least one compound of formula I; more preferably at least one compound of the general formulae I-1 to I-8, I-9; further preferred are compounds of 2 to 10 kinds of the general formulae I-1 to I-8 and I-9.
In some embodiments of the present invention, the liquid crystal compositions of the present invention preferably comprise at least one compound of formula I; more preferably, it contains at least two compounds of the general formulae I-1 to I-8 and I-9.
In some embodiments of the present invention, the liquid crystal compositions of the present invention preferably comprise at least one compound of formula I; more preferably at least two compounds of the formulae I-1 to I-8.
In some embodiments of the present invention, the compounds of formulas I-1 through I-12 are preferably selected from the group consisting of:
Figure RE-GDA0001881743840000083
Figure RE-GDA0001881743840000091
Figure RE-GDA0001881743840000101
Figure RE-GDA0001881743840000111
Figure RE-GDA0001881743840000121
Figure RE-GDA0001881743840000131
Figure RE-GDA0001881743840000141
Figure RE-GDA0001881743840000151
Figure RE-GDA0001881743840000152
and
Figure RE-GDA0001881743840000153
in some embodiments of the invention, the compound of formula I is selected from the group consisting of compounds of formulae I-1-6, formulae I-6-6, formulae I-2-6, formulae I-8-9, formulae I-5-6, and formulae I-4-6.
In some embodiments of the invention, in the compound of formula II, RA2Preferably a linear or branched alkyl or alkoxy group having 1 to 8 carbon atoms, a linear or branched alkenyl or alkenyloxy group having 2 to 8 carbon atoms; further preferred is a linear or branched alkyl group or alkoxy group having 1 to 5 carbon atoms, a linear or branched alkenyl group or alkenyloxy group having 2 to 5 carbon atoms.
In some embodiments of the invention, the ring
Figure RE-GDA0001881743840000154
And ring
Figure RE-GDA0001881743840000155
Each independently represent
Figure RE-GDA0001881743840000156
Figure RE-GDA0001881743840000161
In some embodiments of the invention, LA21、LA22、LA23And LA24Each independently represents-H, -CH3-F or-Cl.
In some embodiments of the invention, the compound of formula ii is selected from the group consisting of:
Figure RE-GDA0001881743840000162
Figure RE-GDA0001881743840000171
Figure RE-GDA0001881743840000181
Figure RE-GDA0001881743840000191
Figure RE-GDA0001881743840000192
and
Figure RE-GDA0001881743840000193
in some embodiments of the present invention, the liquid crystal composition of the present invention preferably comprises at least one compound of formula II; more preferably at least one compound of the general formulae II-1 to II-3, II-15 to II-20, II-25, II-27 to II-43; further preferably 2 to 12 compounds of the general formulae II-1 to II-3, II-15 to II-20, II-25, II-27 to II-43; further preferably 2 to 10 compounds of the general formulae II-1 to II-3, II-15 to II-20, II-25, II-27 to II-43; still more preferably 2 to 8 compounds of the general formulae II-1 to II-3, II-15 to II-20, II-25 and II-27 to II-43.
In some embodiments of the invention, the compound of formula II is selected from the group consisting of compounds of formula II-1, formula II-2, formula II-3, formula II-5, formula II-15, formula II-16, formula II-17, formula II-23, formula II-25, formula II-26, formula II-27, formula II-28, and formula II-34.
The weight percentage of the compound of formula II in the liquid crystal composition of the present invention is preferably: the lower limit of the preferred weight percentage of the compound of formula ii in the liquid crystal composition of the present invention relative to the total weight of the composition of the present invention is 0.1%, 0.5%, 1%, 3%, 5%, 10%, 13%, 14%, 15%, 18%, 20%, 23%, 25%, 28%, 30%, 33%, 35%, 38% or 40%; the upper limit of the percentage by weight of the compound of formula ii in the liquid crystal composition of the invention is preferably 80%, 78%, 75%, 73%, 70%, 68%, 65%, 63%, 60%, 55%, 50%, 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23%, 20%, 18%, 15% or 10% relative to the total weight of the composition of the invention.
In some embodiments of the present invention, the compound of formula II is present in an amount of 0.1% to 80% by weight of the liquid crystal composition.
In some embodiments of the present invention, when it is required to keep the viscosity of the liquid crystal composition of the present invention low and the response time short, the lower limit and the upper limit of the content of the compound of formula ii are preferably slightly lower, wherein the lower limit is preferably: 3%, 5%, 10%, 13%, 14%, 15%, 18%, 20%, 23%, 25%, 28%, 30%, 33%, 35%, 38% or 40%, and the upper limit value is preferably: 70%, 68%, 65%, 63%, 60%, 55%, 50%, 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23% or 20%; further, when it is necessary to keep the clearing point of the liquid crystal composition of the present invention high and the temperature stability is good, the lower limit value and the upper limit value of the content of the compound of the general formula ii are preferably slightly low, wherein the lower limit value is preferably: 5%, 10%, 13%, 14%, 15%, 18%, 20%, 23%, 25%, 28%, 30%, 33%, 35%, 38% or 40%, and the upper limit value is preferably: 65%, 63%, 60%, 55%, 50%, 40%, 38%, 35%, 33%, 30%, 28% or 25%. In addition, when the dielectric anisotropy is increased in order to keep the driving voltage low, the lower limit value and the upper limit value of the content of the compound of the general formula ii are preferably increased, wherein the lower limit value is preferably: 5%, 10%, 13%, 14%, 15%, 18%, 20%, 23%, 25%, 28% or 30%, and the upper limit value is preferably: 55%, 50%, 40%, 38%, 35%, 33%, 30%, 28% or 25%.
In some embodiments of the invention, the compound of formula iii is selected from the group consisting of:
Figure RE-GDA0001881743840000201
Figure RE-GDA0001881743840000211
Figure RE-GDA0001881743840000212
and
Figure RE-GDA0001881743840000213
wherein,
R2represents a linear or branched alkyl or alkoxy group having 1 to 8 carbon atoms or a compound containingStraight or branched chain alkenyl or alkenyloxy of 2 to 8 carbon atoms.
The weight percentage of the compound of formula III in the liquid crystal composition of the present invention is preferably: the preferred lower limit value of the weight percentage of the compound of the general formula iii in the liquid crystal composition of the present invention is 2%, 2.5%, 3%, 5%, 7%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50% or 55% relative to the total weight of the liquid crystal composition of the present invention; the upper limit of the weight percentage of the compound of the general formula iii in the liquid crystal composition of the present invention is preferably 50%, 45%, 40%, 35%, 30% or 25% with respect to the total weight of the liquid crystal composition of the present invention.
In some embodiments of the invention, the compound of formula III is present in an amount of 2% to 50% by weight of the liquid crystal composition.
In some embodiments of the present invention, to improve the contrast in particular, the compound of formula III is preferably selected from the group consisting of compounds of formulae III-a and III-d.
In some embodiments of the present invention, in particular, the compound of formula iii also has the effect of improving the low-temperature miscibility of the liquid crystal composition, and the liquid crystal composition comprising the compound of formula iii has good low-temperature stability.
In some embodiments of the invention, R2Preferably a linear or branched alkyl group having 1 to 5 carbon atoms or a linear or branched alkenyl group having 2 to 5 carbon atoms; further preferably a linear or branched alkyl or alkenyl group having 2 to 5 carbon atoms.
In some embodiments of the invention, in the compounds of formula III-a, R2Preferably represents ethyl, propyl, butyl or pentyl.
The preferred lower limit of the weight percentage of the compound of formula III-a in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0.1%, 1%, 2%, 3%, 5%, 7%, 10%, 12%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; the upper limit of the preferred weight percentage of the compound of the formula III-a in the liquid-crystal composition according to the invention is 50%, 45%, 42%, 40%, 38%, 35%, 33%, 30%, 28%, 26%, 24%, 22%, 20%, 18%, 15%, 12%, 10% or 8%, relative to the total weight of the composition according to the invention.
The preferred lower limit of the weight percentage of the compound of the general formula III-d in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 0.1%, 1%, 2%, 3%, 5%, 7% or 10%; the upper limit of the preferred weight percentage of the compound of the formula III-d in the liquid crystal composition of the invention is 30%, 25%, 20%, 19%, 17%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3%, relative to the total weight of the liquid crystal composition of the invention.
The preferred lower limit of the weight percentage of the compound of the general formula III-b in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 3%, 5%, 8%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; the preferred upper limit value of the weight percentage of the compound of the formula III-b in relation to the total weight of the composition according to the invention in the liquid-crystal composition according to the invention is 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23%, 20%, 19%, 17%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3%.
The preferred lower limit of the weight percentage of the compound of the general formula III-c in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 3%, 5%, 8%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; the preferred upper limit value of the weight percentage of the compound of the formula III-c in the liquid-crystal composition according to the invention is 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23%, 20%, 19%, 17%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3%, relative to the total weight of the composition according to the invention.
The preferred lower limit of the weight percentage of the compound of the general formula III-e in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 3%, 5%, 8%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; the preferred upper limit value of the weight percentage of the compounds of the formulae III-e in the liquid-crystal compositions according to the invention relative to the total weight of the compositions according to the invention is 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23%, 20%, 19%, 17%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3%.
The preferred lower limit of the weight percentage of the compound of the general formula III-f in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 3%, 5%, 8%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; the preferred upper limit value of the weight percentage of the compounds of the general formula III-f in the liquid-crystal composition according to the invention is 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23%, 20%, 19%, 17%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3%, relative to the total weight of the composition according to the invention.
The preferred lower limit of the weight percentage of the compound of the general formula III-g in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 3%, 5%, 8%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; the preferred upper limit of the percentage by weight of the compounds of the formulae III to g relative to the total weight of the composition according to the invention in the liquid-crystal composition according to the invention is 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23%, 20%, 19%, 17%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3%.
The preferred lower limit of the weight percentage of the compounds of the general formulae III to h relative to the total weight of the liquid-crystal composition of the invention in the liquid-crystal composition of the invention is 0%, 1%, 3%, 5%, 8%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; the preferred upper limit value of the weight percentage of the compounds of the formulae III to h relative to the total weight of the composition according to the invention in the liquid-crystal composition according to the invention is 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23%, 20%, 19%, 17%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3%.
In some embodiments of the invention, in the compound of formula M, RM1And RM2Each independently preferably a linear or branched alkyl group having 1 to 10 carbon atoms, a linear or branched alkoxy group having 1 to 9 carbon atoms, a linear or branched alkenyl group having 2 to 10 carbon atoms, or a linear or branched alkenyloxy group having 2 to 10 carbon atoms; further preferably a linear or branched alkyl group having 1 to 8 carbon atoms, a linear or branched alkoxy group having 1 to 7 carbon atoms, or a linear or branched alkenyl group having 2 to 8 carbon atoms; still more preferably a linear or branched alkyl group having 1 to 5 carbon atoms, a linear or branched alkoxy group having 1 to 5 carbon atoms, or a linear or branched alkenyl group having 2 to 5 carbon atoms.
In some embodiments of the invention, preferably, RM1And RM2One or both of them are straight chain or branched chain alkenyl containing 2 to 8 carbon atoms; further preferably, RM1And RM2One or both of them are straight chain or branched chain alkenyl groups having 2 to 5 carbon atoms.
In some embodiments of the invention, preferably, RM1And RM2One is a linear or branched alkenyl group having 2 to 5 carbon atoms, and the other is a linear or branched alkyl group having 1 to 5 carbon atoms.
In some embodiments of the invention, preferably, RM1And RM2Both independently are a linear or branched alkyl group having 1 to 8 carbon atoms or a linear or branched alkoxy group having 1 to 7 carbon atoms; further preferably, each is independently a linear or branched alkyl group having 1 to 5 carbon atoms or a linear or branched alkoxy group having 1 to 4 carbon atoms.
In some embodiments of the invention, preferably, RM1And RM2One is a linear or branched alkyl group having 1 to 5 carbon atoms, and the other is a linear or branched alkyl group having 1 to 5 carbon atoms, or a linear alkyl group having 1 to 4 carbon atomsOr a branched alkoxy group; further preferably, RM1And RM2Both independently are a linear or branched alkyl group having 1 to 5 carbon atoms.
The alkenyl group in the present invention is preferably selected from groups represented by any one of formulae (V1) to (V9), and particularly preferably formula (V1), formula (V2), formula (V8), or formula (V9). The groups represented by formulae (V1) to (V9) are shown below:
Figure RE-GDA0001881743840000241
wherein denotes the carbon atom in the ring structure to which it is bonded.
The alkenyloxy group in the present invention is preferably selected from groups represented by any one of formulae (OV1) to (OV9), and particularly preferably formula (OV1), formula (OV2), formula (OV8), or formula (OV 9). The groups represented by formulae (OV1) to (OV9) are shown below:
Figure RE-GDA0001881743840000242
wherein denotes the carbon atom in the ring structure to which it is bonded.
In some embodiments of the invention, the compound of formula M is selected from the group consisting of:
Figure RE-GDA0001881743840000243
Figure RE-GDA0001881743840000251
Figure RE-GDA0001881743840000252
and
Figure RE-GDA0001881743840000253
in some embodiments of the present invention, the content of the compound of formula M must be properly adjusted depending on desired properties such as solubility at low temperature, transition temperature, electrical reliability, birefringence, process adaptability, drop trace, burn-in, dielectric anisotropy, and the like.
The lower limit of the preferred weight percentage of the compound of formula M in the liquid crystal composition of the present invention with respect to the total weight of the liquid crystal composition of the present invention is 1%, 2%, 3%, 5%, 7%, 10%, 12%, 14%, 16%, 18%, 20%, 22%, 24%, 26%, 28%, 30%, 32%, 34%, 36%, 38%, 40%, 42%, 45%, 48% or 50%; the preferred upper limit of the weight percentage of the compound of formula M in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 38%, 35%, 33%, 30%, 28%, 25%, 22% or 20%.
In some embodiments of the present invention, the compound of formula M comprises 1% to 80% by weight of the liquid crystal composition.
In some embodiments of the present invention, the compound of formula M is particularly preferably selected from the group consisting of compounds of formula M1, formula M2, formula M3, formula M7, formula M8, formula M9, formula M11, formula M12, formula M13, formula M14, formula M17, formula M18, formula M19, formula M20 and formula M21.
In some embodiments of the present invention, where reliability is a concern, compounds of formula M1, formula M2, formula M3, formula M7, formula M8, formula M9, formula M11, formula M12, formula M13, formula M14, formula M17, formula M18, formula M19, formula M20, and formula M21 comprise RM1And RM2Compounds which are all alkyl; when importance is attached to the reduction of the volatility of the compound, the compounds of the general formula M1, the general formula M2, the general formula M3, the general formula M7, the general formula M8, the general formula M9, the general formula M11, the general formula M12, the general formula M13, the general formula M14, the general formula M17, the general formula M18, the general formula M19, the general formula M20, and the general formula M355621 comprises R in the groupM1And RM2Compounds which are all alkoxy groups; and when importance is attached to the reduction in viscosity, R is contained in a group consisting of compounds of formula M1, formula M2, formula M3, formula M7, formula M8, formula M9, formula M11, formula M12, formula M13, formula M14, formula M17, formula M18, formula M19, formula M20 and formula M21M1And RM2A compound in which at least one is alkenyl.
In some embodiments of the present invention, the compound of formula M1 is particularly preferably selected from the group consisting of:
Figure RE-GDA0001881743840000261
Figure RE-GDA0001881743840000262
and
Figure RE-GDA0001881743840000271
wherein,
RM1represents a linear or branched alkyl or alkoxy group having 1 to 8 carbon atoms, or a linear or branched alkenyl or alkenyloxy group having 2 to 8 carbon atoms; and is
RM11And RM21Each independently represents a linear or branched alkyl or alkoxy group containing 1 to 8 carbon atoms.
The weight percentage of the compound of formula M1 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M1 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 1%, 2%, 3%, 5%, 7%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50% or 55%; the upper limit of the preferred weight percentage of the compound of formula M1 in the liquid crystal composition of the invention is 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30% or 25% relative to the total weight of the liquid crystal composition of the invention.
In some embodiments of the invention, the compound of formula M1 is preferably selected from the group consisting of compounds of formula M1-a and formula M1-b.
In some embodiments of the invention, RM1Preferably a linear or branched alkyl group having 1 to 5 carbon atoms or a linear or branched alkenyl group having 2 to 5 carbon atoms; further preferably a linear or branched alkyl or alkenyl group having 2 to 5 carbon atoms.
In some embodiments of the present invention, R in the compounds of the formula M1-a and of the formula M1-b is particularly preferred for the particular improvement of the response timesM1A compound which is ethyl or n-propyl.
R in the compound of the formula M1-a relative to the total weight of the liquid crystal composition of the inventionM1The lower limit value of the compound representing an ethyl group or an n-propyl group in the weight percentage of the liquid crystal composition of the present invention is preferably 0%, 1%, 5%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; r in the compound of formula M1-a relative to the total weight of the composition of the inventionM1The upper limit of the compound representing an ethyl group or an n-propyl group in the liquid crystal composition of the present invention is preferably 60%, 55%, 50%, 45%, 42%, 40%, 38%, 35%, 33%, 30%, 28% or 25% by weight.
R in the compound of the formula M1-b relative to the total weight of the liquid crystal composition of the inventionM1The lower limit value of the compound representing the n-propyl group, which is preferably 0%, 1%, 2%, 3%, 5%, 7% or 10% by weight of the liquid crystal composition of the present invention; r in the compound of the formula M1-b relative to the total weight of the liquid crystal composition of the inventionM1The upper limit value of the compound representing the n-propyl group in the liquid crystal composition of the present invention is preferably 30%, 25%, 20%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3% by weight.
In some embodiments of the invention, in terms of clearing point, when it is desired to obtain a higher clearing point by a compound of formula M1, it is preferredR in the compounds of the formula M1M1A compound represented by butyl or pentyl; further preferred are compounds of the formula M1 wherein RM1A compound represented by n-butyl or n-pentyl.
R in the compounds of the formula M1-a and/or M1-b relative to the total weight of the liquid-crystal composition of the inventionM1The preferred lower limit value of the weight percentage of the compound representing n-butyl or n-pentyl group to the liquid crystal composition of the present invention is 0%, 1%, 3%, 5%, 8%, 10%, 15%, 17%, 20%, 23%, 25%, 27% or 30%; r in the compounds of the formula M1-a and/or M1-b relative to the total weight of the composition of the inventionM1The upper limit value of the compound representing n-butyl or n-pentyl group preferably accounts for 60%, 55%, 50%, 45%, 42%, 40%, 38%, 35%, 33%, 30%, 28%, 25%, 23% or 20% by weight of the liquid crystal composition of the present invention.
The preferred lower limit of the weight percentage of the compound of formula M1-c in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 5%, 10%, 13%, 15%, 17% or 20%; the upper limit value of the compound of the formula M1-c in the weight percent of the liquid crystal composition of the invention is preferably 25%, 23%, 20%, 17%, 15%, 13% or 10% relative to the total weight of the liquid crystal composition of the invention.
The preferred lower limit of the weight percentage of the compound of formula M1-d in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 5%, 10%, 13%, 15%, 17% or 20%; the upper limit value of the compound of the formula M1-d in a weight percentage of the liquid crystal composition of the invention is preferably 25%, 23%, 20%, 17%, 15%, 13% or 10% relative to the total weight of the liquid crystal composition of the invention.
The preferred lower limit of the weight percentage of the compound of formula M1-e to the liquid crystal composition of the invention is 0%, 1%, 5%, 10%, 13%, 15%, 17% or 20% relative to the total weight of the liquid crystal composition of the invention; the upper limit of the preferred weight percentage of the compound of formula M1-e to the liquid crystal composition of the invention is 25%, 23%, 20%, 17%, 15%, 13% or 10% relative to the total weight of the liquid crystal composition of the invention.
The preferred lower limit of the weight percentage of the compound of formula M1-f in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 5%, 10%, 13%, 15%, 17% or 20%; the upper limit value of the compound of formula M1-f in the weight percent of the liquid crystal composition of the invention is preferably 25%, 23%, 20%, 17%, 15%, 13% or 10% relative to the total weight of the liquid crystal composition of the invention.
The preferred lower limit of the weight percentage of the compound of formula M1-g to the liquid crystal composition of the invention is 0%, 1%, 5%, 10%, 13%, 15%, 17% or 20% relative to the total weight of the liquid crystal composition of the invention; the upper limit of the preferred weight percentage of the compound of formula M1-g to the liquid crystal composition of the invention is 25%, 23%, 20%, 17%, 15%, 13% or 10% relative to the total weight of the liquid crystal composition of the invention.
In some embodiments of the invention, R in compounds of formula M1-f and/or formula M1-g is preferredM1A compound which is ethyl or n-propyl.
R in the compounds of the formula M1-f and/or M1-g relative to the total weight of the liquid-crystal composition of the inventionM1The preferred lower limit of the weight percentage of the compound being ethyl or n-propyl in the liquid crystal composition of the present invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 13%, 15%, 18% or 20%; r in the compounds of the formula M1-f and/or M1-g relative to the total weight of the liquid-crystal composition of the inventionM1The upper limit of the preferred weight percentage of the compound which is ethyl or n-propyl in the liquid crystal composition of the present invention is 20%, 17%, 15%, 13%, 10%, 8%, 7% or 6%.
In some embodiments of the invention, R in the compound of formula M1-hM11Represents a straight-chain or branched alkyl or alkoxy group having 1 to 7 carbon atoms; more preferably a linear or branched chain having 1 to 5 carbon atomsAlkyl or alkoxy.
The preferred lower limit of the weight percentage of the compound of formula M1-h to the liquid crystal composition of the invention is 0%, 1%, 3%, 5%, 7%, 10%, 13%, 15%, 17%, 20%, 23%, 25% or 30% relative to the total weight of the liquid crystal composition of the invention; the preferred upper limit of the weight percentage of the compound of formula M1-h to the liquid crystal composition of the invention is 60%, 55%, 50%, 45%, 40%, 37%, 35%, 33%, 30%, 27%, 25%, 23%, 20%, 17%, 15%, 13% or 10% relative to the total weight of the liquid crystal composition of the invention.
In some embodiments of the present invention, R in the compounds of formula M1-h is preferred in order to improve especially the response time of the liquid crystal compositions of the present inventionM11Is ethyl, n-propyl, butyl or pentyl, and RM21A compound that is methyl or methoxy; r in the compounds of the formula M1-hM11Is ethyl, n-propyl, butyl or pentyl, and RM21A compound that is ethyl or ethoxy; or R in the compounds of the formula M1-hM11Is n-propyl, butyl or pentyl, and RM21A compound that is n-propyl or propoxy.
R in the compounds of the formula M1-h relative to the total weight of the liquid-crystal composition of the inventionM11Is n-propyl and RM21The preferred lower limit value of the weight percentage of the compound which is an ethyl group in the liquid crystal composition of the present invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 13%, 15%, 18% or 20%; r in the compounds of the formula M1-h relative to the total weight of the liquid-crystal composition of the inventionM11Is n-propyl and RM21The upper limit of the preferred weight percentage of the compound which is an ethyl group in the liquid crystal composition of the present invention is 20%, 17%, 15%, 13%, 10%, 8%, 7% or 6%.
The weight percentage of the compound of formula M2 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M2 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7% or 10%; the upper limit of the preferred weight percentage of the compound of formula M2 in the liquid crystal composition of the invention is 20%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3% relative to the total weight of the liquid crystal composition of the invention.
The weight percentage of the compound of formula M3 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M3 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7% or 10%; the upper limit of the preferred weight percentage of the compound of formula M3 in the liquid crystal composition of the invention is 20%, 15%, 13%, 10%, 8%, 7%, 6%, 5% or 3% relative to the total weight of the liquid crystal composition of the invention.
The weight percentage of the compound of formula M7 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M7 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 14%, 16%, 20%, 23%, 26%, 30%, 35% or 40%; the upper limit of the preferred weight percentage of the compound of formula M7 in the liquid crystal composition of the invention is 50%, 40%, 35%, 30%, 20%, 15%, 10% or 5% relative to the total weight of the liquid crystal composition of the invention.
In some embodiments of the present invention, it is preferable to contain R in the compound of the formula M7 in view of required properties of solubility at low temperature, transition temperature, electrical reliability, birefringence and the likeM1Is a linear or branched alkenyl radical having 2 to 4 carbon atoms, and RM2Is CH3The compound of (a), the straight-chain or branched alkenyl group having 2 to 4 carbon atoms is more preferably
Figure RE-GDA0001881743840000301
R in the compound of formula M7 relative to the total weight of the liquid crystal composition of the inventionM1Is composed of
Figure RE-GDA0001881743840000302
And R isM2Is CH3The lower limit of the weight percentage of the compound of (a) to the liquid crystal composition of the present invention is preferably 0%, 1%, 3%, 5%, 7%, 9%, 11%, 12%, 13%, 18% or 21%, and the upper limit is preferably 45%, 40%, 35%, 30%, 25%, 23%, 20%, 18%, 15%, 13%, 10% or 8%. When both the two compounds are contained, the lower limit of the weight percentage of the two compounds in the liquid crystal composition of the present invention is preferably 2%, 3%, 5%, 7%, 9%, 11%, 13%, 15%, 19%, 24% or 30%, and the upper limit thereof is preferably 45%, 40%, 35%, 30%, 25%, 23%, 20%, 18%, 15%, 13%, 11%, 9%, 7% or 5%, with respect to the total weight of the liquid crystal composition of the present invention.
The weight percentage of the compound of formula M8 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M8 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 4%, 5%, 7%, 10%, 14%, 16% or 20%; the preferred upper limit value of the weight percentage of the compound of formula M8 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 40%, 35%, 30%, 20%, 15%, 10% or 5%.
In some embodiments of the present invention, it is preferable to contain R in the compound of the formula M8 in view of required properties of solubility at low temperature, transition temperature, electrical reliability, birefringence and the likeM1Is a linear or branched alkenyl radical having 2 to 4 carbon atoms, and RM2Is CH3The compound of (a), the straight-chain or branched alkenyl group having 2 to 4 carbon atoms is more preferably
Figure RE-GDA0001881743840000303
R in the compound of formula M8 relative to the total weight of the liquid crystal composition of the inventionM1Is composed of
Figure RE-GDA0001881743840000304
And R isM2Is CH3The lower limit of the weight percentage of the compound of (a) to the liquid crystal composition of the present invention is preferably 0%, 1%, 3%, 4%, 5%, 7%, 9%, 11%, 12%, 13%, 18% or 20%, and the upper limit is preferably 40%, 35%, 30%, 25%, 23%, 20%, 18%, 15%, 13%, 10% or 8%. When both the two compounds are contained, the lower limit value of the weight percentage of the two compounds in the liquid crystal composition of the present invention is preferably 3%, 5%, 7%, 9%, 11%, 13%, 15%, 19%, 24% or 30%, and the upper limit value is preferably 40%, 35%, 30%, 25%, 23%, 20%, 18%, 15% or 13%, with respect to the total weight of the liquid crystal composition of the present invention.
The weight percentage of the compound of formula M9 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M9 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 14%, 16%, 20%, 23%, 26%, 30%, 35% or 40%; the upper limit of the preferred weight percentage of the compound of formula M9 in the liquid crystal composition of the invention is 50%, 40%, 35%, 30%, 20%, 15%, 10% or 5% relative to the total weight of the liquid crystal composition of the invention.
In some embodiments of the invention, the compound of formula M9 is preferably RM1Is ethyl, propyl, butyl or pentyl, and RM2A compound that is methyl or ethyl; or preferably RM1Is composed of
Figure RE-GDA0001881743840000311
And R isM2A compound that is methyl, ethyl or n-propyl; or preferably RM1Is n-propyl, n-butyl or n-pentyl, and RM2Is CH3A compound of O-.
The weight percentage of the compound of formula M11 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M11 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 14%, 16%, 20%, 23%, 26%, 30%, 35% or 40%; the upper limit of the preferred weight percentage of the compound of formula M11 in the liquid crystal composition of the invention is 50%, 40%, 35%, 30%, 20%, 15%, 10% or 5% relative to the total weight of the liquid crystal composition of the invention.
In some embodiments of the invention, the compound of formula M11 is preferably RM1And RM2Each independently represents a linear or branched alkyl group having 2 to 5 carbon atoms, or preferably RM1And RM2One of them is
Figure RE-GDA0001881743840000312
Figure RE-GDA0001881743840000313
And the other is CH3-or C2H5-a compound of (a).
The weight percentage of the compound of formula M12 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M12 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 12%, 14%, 16%, 18%, 20%, 23%, 26%, 30%, 35% or 40%; the upper limit of the preferred weight percentage of the compound of formula M12 in the liquid crystal composition of the invention is 50%, 40%, 35%, 30%, 25%, 22%, 20%, 18%, 15%, 12%, 10%, 8% or 5% relative to the total weight of the liquid crystal composition of the invention.
The weight percentage of the compound of formula M13 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M13 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 12%, 14%, 16%, 18%, 20%, 23%, 26%, 30%, 35% or 40%; the upper limit of the preferred weight percentage of the compound of formula M13 in the liquid crystal composition of the invention is 50%, 40%, 35%, 30%, 25%, 22%, 20%, 18%, 15%, 12%, 10%, 8% or 5% relative to the total weight of the liquid crystal composition of the invention.
The weight percentage of the compound of formula M14 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M14 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 12%, 14%, 16%, 18%, 20%, 23%, 26%, 30%, 35% or 40%; the upper limit of the preferred weight percentage of the compound of formula M14 in the liquid crystal composition of the invention is 50%, 40%, 35%, 30%, 25%, 22%, 20%, 18%, 15%, 12%, 10%, 8% or 5% relative to the total weight of the liquid crystal composition of the invention.
The weight percentage of the compound of formula M15 in the liquid crystal composition of the invention is preferably: the preferred lower limit of the weight percentage of the compound of formula M15 in the liquid crystal composition of the invention relative to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 12%, 14%, 16%, 18%, 20%, 23%, 26%, 30%, 35% or 40%; the upper limit of the preferred weight percentage of the compound of formula M15 in the liquid crystal composition of the invention is 50%, 40%, 35%, 30%, 25%, 22%, 20%, 18%, 15%, 12%, 10%, 8% or 5% relative to the total weight of the liquid crystal composition of the invention.
The weight percentage of the compounds of formulae M17 to M21 in the liquid crystal composition of the present invention is preferably: the lower limit of the preferred percentage of the compounds of formulae M17 to M21 to the total weight of the liquid crystal composition of the invention is 0%, 1%, 2%, 3%, 5%, 7%, 10%, 14%, 16% or 20%; the upper limit value of the compound of the general formula M17 to M21 in the total weight percentage of the liquid crystal composition of the present invention is preferably 30%, 25%, 23%, 20%, 18%, 15%, 12%, 10% or 5% relative to the total weight of the liquid crystal composition of the present invention.
In some embodiments of the present invention, the liquid crystal composition further comprises at least one compound of formula A-1, said compound of formula A-1 having a positive dielectric anisotropy:
Figure RE-GDA0001881743840000321
wherein,
RA1represents a linear or branched alkyl group having 1 to 12 carbon atoms,
Figure RE-GDA0001881743840000322
1 or non-adjacent 2 or more-CH in the linear or branched alkyl containing 1 to 12 carbon atoms2-said linear or branched alkyl radical containing from 1 to 12 carbon atoms which may be independently replaced by-CH ═ CH-, -C ≡ C-, -O-, -CO-O-or-O-CO-, respectively,
Figure RE-GDA0001881743840000323
Each of one or more-H may be independently substituted with-F or-Cl;
ring (C)
Figure RE-GDA0001881743840000324
And ring
Figure RE-GDA0001881743840000325
Each independently represent
Figure RE-GDA0001881743840000326
Figure RE-GDA0001881743840000331
Wherein,
Figure RE-GDA0001881743840000332
up to 1-CH in2-may be replaced by-O-, one or moreThe single bonds in the ring may be replaced by double bonds,
Figure RE-GDA0001881743840000333
may be substituted by-CN, -F or-Cl, and one or more rings may be substituted by-CH ═ by-N;
ZA11represents a single bond, -CH2CH2-、-CF2CF2-、-CO-O-、-O-CO-、-O-CO-O-、-CH＝CH-、-CF ＝CF-、-CH2O-or-OCH2-；
LA11、LA12And LA13Each independently represents-H, -F or-CH3；
XA1Represents halogen, haloalkyl or haloalkoxy having 1 to 5 carbon atoms, haloalkenyl or haloalkenyloxy having 2 to 5 carbon atoms; and is
nA1Represents 0, 1, 2 or 3, and when nA1When 2 or 3, ring
Figure RE-GDA0001881743840000334
May be the same or different, ZA11May be the same or different.
In some embodiments of the present invention, the compound of formula A-1 is preferably a compound having an absolute value of dielectric anisotropy greater than 4.
In some embodiments of the invention, the compound of formula A-1 is selected from the group consisting of:
Figure RE-GDA0001881743840000335
Figure RE-GDA0001881743840000341
Figure RE-GDA0001881743840000351
Figure RE-GDA0001881743840000361
Figure RE-GDA0001881743840000371
Figure RE-GDA0001881743840000372
and
Figure RE-GDA0001881743840000373
wherein,
RA1represents a linear or branched alkyl group having 1 to 12 carbon atoms, 1 or not adjacent 2 or more-CH in the linear or branched alkyl group having 1 to 12 carbon atoms2-may be independently replaced by-CH ═ CH-, -C ≡ C-, -O-, -CO-O-, or-O-CO-, respectively.
The weight percentage of the compound of formula A-1 to the liquid crystal composition of the present invention is preferably: the preferred lower limit of the weight percentage of the compound of formula a-1 to the liquid crystal composition of the present invention is 0%, 1%, 5%, 10%, 12%, 15%, 18%, 20%, 30%, 40%, 50%, 55%, 60%, 65%, 70%, 75% or 80% relative to the total weight of the liquid crystal composition of the present invention; the preferred upper limit value of the weight percentage of the compound of the general formula a-1 to the liquid crystal composition of the present invention is 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30% or 25% relative to the total weight of the liquid crystal composition of the present invention.
In some embodiments of the present invention, the compound of formula A-1 is preferably selected from the group consisting of compounds of formulae A-1-5, formulae A-1-13, formulae A-1-22, formulae A-1-23, formulae A-1-24, formulae A-1-27, formulae A-1-30, formulae A-1-31, formulae A-1-35, formulae A-1-40, and formulae A-1-44.
In addition to the above compounds, the liquid crystal composition of the present invention may contain a conventional nematic liquid crystal, smectic liquid crystal, cholesteric liquid crystal, antioxidant, ultraviolet absorber, infrared absorber, polymerizable monomer, light stabilizer, and the like.
Possible dopants which are preferably added to the liquid crystal composition according to the invention are shown below.
Figure RE-GDA0001881743840000374
Figure RE-GDA0001881743840000381
Figure RE-GDA0001881743840000382
And
Figure RE-GDA0001881743840000383
in some embodiments of the present invention, preferably, the dopant comprises 0-5% by weight of the liquid crystal composition; more preferably, the dopant is present in an amount of 0-1% by weight of the liquid crystal composition.
Further, additives such as an antioxidant and a light stabilizer used in the liquid crystal composition of the present invention are preferably as follows:
Figure RE-GDA0001881743840000391
Figure RE-GDA0001881743840000401
Figure RE-GDA0001881743840000411
wherein n represents a positive integer of 1 to 12.
Preferably, the light stabilizer is selected from the group consisting of the light stabilizers shown below:
Figure RE-GDA0001881743840000412
Figure RE-GDA0001881743840000421
in some embodiments of the present invention, preferably, the light stabilizer is 0 to 5% by weight of the total liquid crystal composition; more preferably, the light stabilizer is 0-1% by weight of the total liquid crystal composition; particularly preferably, the light stabilizer is 0 to 0.1% by weight based on the total weight of the liquid crystal composition.
In some embodiments of the present invention, the clearing point Cp of the liquid crystal composition is in the range of 80 to 120 ℃, preferably 85 to 110 ℃, and more preferably 90 to 110 ℃; the dielectric anisotropy Δ ∈ is in the range of 6 to 12, preferably 7 to 11, further preferably 7.5 to 10.5, further preferably 8 to 10.5; the optical anisotropy Δ n is in the range of 0.08 to 0.12, preferably 0.085 to 0.115, more preferably 0.09 to 0.11, more preferably 0.09 to 0.105; average elastic constant KaveNot less than 13.9; the transmittance T is not lower than 12.5%; low temperature transformation point TS→NGreater than-30 ℃ and the storage time is greater than 7 days.
In another aspect, the present invention also provides a liquid crystal display device comprising the above liquid crystal composition.
Has the advantages that:
the liquid crystal composition provided by the invention has high dielectric anisotropy, appropriately high optical anisotropy, appropriately high clearing point, high transmittance, good low-temperature stability and larger KaveSo that the liquid crystal display device comprising the liquid crystal composition has higher contrast ratio, relatively less light scattering and good display effect. In particular, in the liquid crystal composition of the present invention, when a compound of the formula I is addedWhen the compound is used, the liquid crystal composition has higher transmittance, so that the compound shown in the general formula I can improve the transmittance of the liquid crystal composition, and a liquid crystal display device containing the liquid crystal composition has higher contrast; when the compound of the formula III is added, the low-temperature mutual solubility of the liquid crystal composition can be improved. The inventors of the present invention have surprisingly found that liquid crystal compositions of the present invention comprising compounds of formula I, formula II, formula III, and formula M can achieve a large average elastic constant KaveThe liquid crystal display device can obtain relatively less light scattering and higher contrast ratio, so the liquid crystal composition can obtain good display effect of the liquid crystal display device.
Detailed Description
The invention will be illustrated below with reference to specific embodiments. It should be noted that the following examples are illustrative of the present invention, and are not intended to limit the present invention. Other combinations and various modifications within the spirit or scope of the present invention may be made without departing from the spirit or scope of the present invention.
For convenience of expression, in the following examples, the group structure of the liquid crystal composition is represented by the code listed in Table 1:
TABLE 1 radical structural code of liquid crystal compounds
Figure RE-GDA0001881743840000431
Compounds of the following formula are exemplified:
Figure RE-GDA0001881743840000441
the structural formula is represented by the code listed in Table 1, and can be expressed as: nCCGF, wherein n in the code represents the number of C atoms of the left alkyl group, for example, n is 3, namely, the alkyl group is-C3H7(ii) a C in the code represents cyclohexane, G represents 2-fluoro-1, 4-phenylene and F represents fluorine.
The abbreviated codes of the test items in the following examples are as follows:
cp clearing Point (nematic phase-transition temperature of isotropic phase,. degree.C.)
TS→NLow temperature transformation Point (smectic-nematic transition temperature,. degree.C.)
Δ n optical anisotropy (589nm, 25 ℃ C.)
Delta epsilon dielectric anisotropy (1KHz, 25 ℃ C.)
K11Elastic constant ("splay", pN at 20 ℃ C.)
K22Elastic constant ("distortion", pN at 20 ℃ C.)
K33Elastic constant ("bending", pN at 20 ℃ C.)
KaveAverage elastic constant (K)11+K22+K33Average value of (1)
T transmittance (DMS 505 tester, box thickness 3.5 μm)
LTS Low temperature stability
Wherein,
the optical anisotropy was measured using an Abbe refractometer under a sodium lamp (589nm) light source at 25 ℃.
Δε＝ε‖-ε⊥Wherein, epsilon‖Is a dielectric constant parallel to the molecular axis,. epsilon⊥For the dielectric constant perpendicular to the molecular axis, test conditions: the test box is TN90 type at 25 deg.C and 1KHz, and has a thickness of 7 μm.
K11、K22、K33The liquid crystal display device is obtained by using an LCR instrument and an antiparallel friction box to test a C-V curve of liquid crystal and calculating the following test conditions: a 7-micron antiparallel friction box, wherein V is 0.1-20V;
Figure RE-GDA0001881743840000442
(K11+K22+K33)。
test conditions for T transmittance: and testing the transmittance of the dimming device at the clearing point +/-10 ℃ by using a DMS 505 tester, wherein the thickness of the box of the dimming device is 3.5 mu m of the IPS type liquid crystal test box.
The components used in the following examples can be synthesized by a known method or obtained commercially. These synthesis techniques are conventional, and the resulting liquid crystal compounds were tested to meet the standards for electronic compounds.
Liquid crystal compositions were prepared according to the compounding ratios of the liquid crystal compositions specified in the following examples. The liquid crystal composition is prepared according to the conventional method in the field, such as heating, ultrasonic wave, suspension and the like, and is mixed according to the specified proportion.
Liquid crystal compositions given in the following examples were prepared and studied. The composition of each liquid crystal composition and the results of the performance parameter test thereof are shown below.
Comparative example 1
The liquid crystal composition of comparative example 1, which was filled between two substrates of a liquid crystal display and subjected to a performance test, was prepared by the respective compounds and weight percentages listed in table 2.
TABLE 2 liquid crystal composition formulation and Performance parameter testing
Figure RE-GDA0001881743840000451
Example 1
The liquid crystal composition of example 1 was prepared according to the compounds and weight percentages listed in table 3, and filled between two substrates of a liquid crystal display for performance testing.
TABLE 3 liquid crystal composition formulation and Performance parameter testing
Figure RE-GDA0001881743840000452
Figure RE-GDA0001881743840000461
Example 2
The liquid crystal composition of example 2 was prepared according to the compounds and weight percentages listed in table 4, and filled between two substrates of a liquid crystal display for performance testing.
TABLE 4 liquid crystal composition formulation and Performance parameter testing
Figure RE-GDA0001881743840000462
Figure RE-GDA0001881743840000471
Example 3
The liquid crystal composition of example 3 was prepared according to the compounds and weight percentages listed in table 5, and filled between two substrates of a liquid crystal display for performance testing.
TABLE 5 liquid Crystal composition formulations and Performance parameter testing
Figure RE-GDA0001881743840000472
Example 4
The liquid crystal composition of example 4 was prepared according to the compounds and weight percentages listed in table 6, and filled between two substrates of a liquid crystal display for performance testing.
TABLE 6 liquid crystal composition formulation and Performance parameter testing
Figure RE-GDA0001881743840000481
Example 5
The liquid crystal composition of example 5 was prepared according to the compounds and weight percentages listed in table 7, and filled between two substrates of a liquid crystal display for performance testing.
TABLE 7 liquid Crystal composition formulations and Performance parameter testing
Figure RE-GDA0001881743840000482
Figure RE-GDA0001881743840000491
As is clear from the above comparative example 1 and examples 1 to 5, the liquid crystal composition provided by the present invention has high dielectric anisotropy, suitably high optical anisotropy, suitably high clearing point, high transmittance, good low temperature stability, and large KaveSo that the liquid crystal display device comprising the liquid crystal composition has higher contrast ratio, relatively less light scattering and good display effect.
The above embodiments are merely illustrative of the technical concept and features of the present invention, and the present invention is not limited thereto, and equivalent changes and modifications made according to the spirit of the present invention should be covered thereby.

Claims (6)

1. A liquid crystal composition, comprising:
3% -30% of at least one compound selected from the group consisting of compounds of the general formulae I-2 to I-5 and I-7 to I-8
Figure FDA0003388964050000011
1-50% of at least one compound of formula II
Figure FDA0003388964050000012
4% to 25% of at least one compound selected from the group consisting of compounds of the formula III-a and compounds of the formula III-e
Figure FDA0003388964050000013
And
10-60% of at least one compound of formula M
Figure FDA0003388964050000021
Wherein,
R1and RA2Each independently represents a linear or branched alkyl group having 1 to 12 carbon atoms,
Figure FDA0003388964050000022
Figure FDA0003388964050000023
1 or non-adjacent 2 or more-CH in the linear or branched alkyl containing 1 to 12 carbon atoms2-said linear or branched alkyl containing 1 to 12 carbon atoms, which may be independently replaced by-C ═ C-, -C ≡ C-, -O-, -CO-O-or-O-CO-, respectively,
Figure FDA0003388964050000024
Each of one or more-H may be independently substituted with-F or-Cl;
R2represents a linear or branched alkyl or alkoxy group having 1 to 8 carbon atoms, or a linear or branched alkenyl or alkenyloxy group having 2 to 8 carbon atoms;
RM1and RM2Each independently represents-H, a linear or branched alkyl group having 1 to 12 carbon atoms, a linear or branched alkenyl group having 2 to 12 carbon atoms,
Figure FDA0003388964050000025
1 or non-adjacent 2 or more-CH in the linear or branched alkyl containing 1 to 12 carbon atoms2Can be independently activated respectivelyC.ident.C-, -O-, -CO-O-or-O-CO-substitution;
ring (C)
Figure FDA0003388964050000026
And ring
Figure FDA0003388964050000027
Each independently represent
Figure FDA0003388964050000028
Wherein,
Figure FDA0003388964050000029
one or more-CH2-may be replaced by-O-, one or more of the ring single bonds may be replaced by double bonds,
Figure FDA00033889640500000210
may be substituted by-CN, -F or-Cl, and one or more rings may be substituted by-CH ═ by-N;
ring (C)
Figure FDA00033889640500000211
Ring (C)
Figure FDA00033889640500000212
And ring
Figure FDA00033889640500000213
Each independently represent
Figure FDA00033889640500000214
Figure FDA00033889640500000215
Wherein
Figure FDA00033889640500000216
One or more-CH of2-can be replaced by-O-,
Figure FDA00033889640500000217
at most one-H in (a) may be substituted by halogen;
ZA21and ZA22Each independently represents a single bond, -CH2CH2-、-CF2CF2-、-CO-O-、-O-CO-、-O-CO-O-、-CH＝CH-、-CF＝CF-、-CH2O-or-OCH2-；
ZM1And ZM2Each independently represents a single bond, -CO-O-, -O-CO-, -CH2O-、-OCH2-、-CH＝CH-、-C≡C-、-CH2CH2-or- (CH)2)4-；
L1、L2、L4、LA21、LA22、LA23And LA24Each independently represents-H, an alkyl group having 1 to 3 carbon atoms, or a halogen;
L5represents-H or-F;
Rxand RyEach independently represents-CH2-or-O-;
x represents halogen, haloalkyl or haloalkoxy having 1 to 5 carbon atoms, haloalkenyl or haloalkenyloxy having 2 to 5 carbon atoms;
XA2represents halogen, haloalkyl or haloalkoxy having 1 to 5 carbon atoms, haloalkenyl or haloalkenyloxy having 2 to 5 carbon atoms;
nA2represents 0, 1, 2 or 3, and when nA2When 2 or 3, ring
Figure FDA0003388964050000031
May be the same or different, ZA21May be the same or different;
nM1represents 0, 1, 2 or 3, and when nM1When 2 or 3, ring
Figure FDA0003388964050000032
May be the same or different, ZM2May be the same or different;
when Z isA21And ZA22Represents a single bond, nA2Denotes 1, ring
Figure FDA0003388964050000033
To represent
Figure FDA0003388964050000034
Ring (C)
Figure FDA0003388964050000035
Represents one or more of-H which may be substituted by-F or-Cl
Figure FDA0003388964050000036
When L isA21、LA22、LA23And LA24At least one is not-H; and is
When the ring
Figure FDA0003388964050000037
And ring
Figure FDA0003388964050000038
Is one of
Figure FDA0003388964050000039
When n is greater than nA2Represents 1.
2. The liquid crystal composition of claim 1, wherein the ring is
Figure FDA00033889640500000310
And ring
Figure FDA00033889640500000311
Each independently represent
Figure FDA00033889640500000312
Figure FDA00033889640500000313
3. Liquid crystal composition according to claim 1 or 2, characterized in that the compound of formula ii is selected from the group consisting of:
Figure FDA00033889640500000314
Figure FDA0003388964050000041
Figure FDA0003388964050000051
Figure FDA0003388964050000061
Figure FDA0003388964050000071
and
Figure FDA0003388964050000072
4. the liquid crystal composition according to claim 1, wherein the at least one compound selected from the group consisting of a compound of formula III-a and a compound of formula III-e is the compound of formula III-a:
Figure FDA0003388964050000073
5. the liquid crystal composition of claim 1, wherein the compound of formula M is selected from the group consisting of:
Figure FDA0003388964050000074
Figure FDA0003388964050000081
Figure FDA0003388964050000082
and
Figure FDA0003388964050000083
6. a display device comprising the liquid crystal composition according to any one of claims 1 to 5.
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