CN107815322B - Liquid crystal compound, liquid crystal composition and display device - Google Patents

Liquid crystal compound, liquid crystal composition and display device Download PDF

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CN107815322B
CN107815322B CN201610825423.6A CN201610825423A CN107815322B CN 107815322 B CN107815322 B CN 107815322B CN 201610825423 A CN201610825423 A CN 201610825423A CN 107815322 B CN107815322 B CN 107815322B
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liquid crystal
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韩文明
徐爽
徐海彬
陈昭远
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Jiangsu Hecheng Display Technology Co Ltd
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    • C09K19/3001Cyclohexane rings
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    • C09K19/08Non-steroidal liquid crystal compounds containing at least two non-condensed rings
    • C09K19/30Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
    • C09K19/3001Cyclohexane rings
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Abstract

The invention provides a liquid crystal composition and application thereof, wherein the liquid crystal composition comprises: 1-20% by weight of the total liquid crystal composition of at least one compound of formula I; 25-80% by total weight of the liquid crystal composition of at least one compound selected from the group consisting of formula II-1, formula II-2, formula II-3, formula II-4, and combinations thereof; and 20-75% by total weight of the liquid crystal composition of at least one compound selected from the group consisting of formula III-1, III-2, III-3, III-4, and combinations thereof. The liquid crystal composition has proper optical anisotropy, higher clearing point, larger negative dielectric anisotropy, low viscosity and high reliability, is suitable for a liquid crystal display, and meets the requirement of quick response of the liquid crystal display. The invention also provides a compound corresponding to the general formula I-2.

Description

Liquid crystal compound, liquid crystal composition and display device
Technical Field
The present invention relates to a liquid crystal compound and a liquid crystal composition, and more particularly, to a liquid crystal composition having suitable optical anisotropy, a high clearing point, a large negative dielectric anisotropy, a low viscosity, and high reliability, and a liquid crystal display device including the same.
Background
It is well known that compounds of the formula M
Figure GDA0002662916930000011
Can be used for active matrix addressed electro-optical displays based on the ECB effect, IPS (in plane switching) displays or FFS (fringe field switching) displays.
The principle of the electrically controlled birefringence, the ECB effect or also the DAP (aligned phase distortion) effect was first described in 1971 (M.F. Schieckel and K.Fahrenschon, "Deformation of biological liquid crystals with vertical orientation in electrical fields", applied. Phys. Lett.19(1971), 3912). This is followed by papers from j.f. kahn (appl.phys.lett.20(1972),1193) and g.labrunie and j.robert (j.appl.phys.44(1973), 4869).
The papers of J.Robert, F.Clerc (SID80Digest techn. papers (1980),30), J.Duchene (Displays7(1986),3) and H.Schad (SID82Digest techn. papers (1982),244) show that the liquid-crystalline phase must have a high number of elastic constant ratios K3/K1High values of optical anisotropy Deltan and Deltasinum are less than or equal to 0.5, and are suitable for high-information display elements based on the ECB effect. Electro-optical display elements based on the ECB effect have a homeotropic edge alignment (VA technique ═ vertical alignment). Dielectrically negative liquid-crystalline media can also be used in displays which utilize the so-called IPS or FFS effect.
Displays using the ECB effect, as so-called WAN (vertically aligned nematic) displays, are described, for example, in MVA (Multi-Domain vertical alignment, e.g. Yoshide, H. et al, article 3.1: "MAA LCD for Notebook or Mobile PCs.", SID2004International Syspossium, Digest of Technical Papers, XXXV, edition I, pages 6-9, and Liu, C.T. et al, article 15.1: "A46 in TFT LCD HDTV. technical., SID2004International Syosium, Digest of Technical Papers, XXXV, edition II, page 750. 753), PVA (patterned vertical alignment, e.g. Kim, SangSoo, article 15.4:" Super New State of PVA ", PVA of device for the" PVA (PVA of the same, see FIG. 13, High-level of Technical field, see FIG. 13, S.: Sk. S, S. Softx, S. Sk. TM., "FIGS.;, S. Softn. Softx. Sk. Softx. Sk. Softx. et al, see FIGS.;" FIGS. 13. 12. Softx. Sk. Softx. Softs. Sk. In Digest of Technical Papers, XXXV, edition II, page 754757) mode, it has been determined per se that in addition to IPS (in-plane switching) displays (for example: yeo, s.d., paper 15.3: "An LC Display for the TV Application", SID2004International Symposium, Digest of Technical Papers, XXXV, edition II, pages 758 and 759) and the long known TN (twisted nematic) displays, one of the three more recent types of liquid crystal displays of current importance, in particular for TV applications. For example, in Souk, Jun, SID semiar 2004, semiar M6: "Recent Advances in LCD Technology", serum signatures, M6/1 to M6/26, and Miller, Ian, SID serum 2004, serum M7: these techniques are compared in the usual manner in "LCD Television", serum features Notes, M7/1 to M7/32. Although the response time of modern ECB displays has been significantly improved by overdrive (over drive) addressing methods, for example: kim, Hyeon Kyeong et al, article 9.1: "A57 in. Wide UXGA TFT LCD for HDTV Application", SID2004International Symposium, Digest of Technical Papers, XXXV, edition I, page 106 and 109, but obtaining a response time suitable for video, particularly in gray scale switching, is still a problem that is not satisfactorily solved.
The industrial application of this effect in electro-optical display elements requires that the liquid crystal phase must meet a number of requirements. Of particular importance here are chemical resistance to moisture, air and physical influences such as heat, infrared, visible light, ultraviolet radiation and direct and alternating electric fields.
Furthermore, the industrially available liquid crystalline phase requires the characteristics of a liquid crystalline mesophase and low viscosity in a suitable temperature range.
None of the series of compounds having a liquid crystalline mesophase disclosed to date comprises a single compound that meets all these requirements. Thus, mixtures of two to twenty-five, preferably three to eighteen compounds are generally prepared to obtain materials which can be used as liquid crystalline phases. However, since no liquid crystal material having a significantly negative dielectric anisotropy and sufficient long-term stability has been available so far, it has not been possible to easily prepare an optimum phase in this manner.
Matrix liquid crystal displays (MLC displays) are known. Non-linear elements such as active elements (i.e. transistors) that can be used for individual pixel independent switching. Thus, the term "active matrix" is used, wherein two types can be distinguished:
1. a MOS (metal oxide semiconductor) transistor on a silicon wafer as a substrate;
2. a Thin Film Transistor (TFT) on a glass plate as a substrate.
In the case of type 1, the electro-optical effect used is usually a dynamic scattering or guest-host effect. The use of single crystal silicon as a substrate material limits the display size, since even modular assembly of various sub-displays can cause problems at the joints.
In the case of the preferred more promising type 2, the electro-optical effect used is generally the TN effect.
There is a distinction between the two techniques: TFTs containing compound semiconductors such as CdSe, or TFTs based on polycrystalline or amorphous silicon. With respect to the latter technique, intensive work is being performed worldwide.
The TFT matrix is applied to the inside of one glass plate of the display, while the other glass plate carries a transparent counter electrode on its inside. The TFT is very small compared to the size of the pixel electrode and has little adverse effect on the image. The technique can also be generalized for full-color displays where a mosaic of red, green and blue filters can have filter elements arranged in opposition to each switchable pixel.
The term MLC display here encompasses any matrix display with integrated non-linear elements, i.e. in addition to an active matrix also displays with passive elements, such as variable resistors or diodes (MIM ═ metal-insulator-metal).
Such MLC displays are particularly suitable for TV applications (e.g. pocket TVs) or for high-information displays in automobile or aircraft construction. In addition to the problems with respect to the angle dependence of the contrast and the response time, difficulties also arise in MLC displays due to the insufficiently high specific resistance of the liquid-crystal mixture [ TOGASHI, s., SEKIGUCHI, k., TANABE, h., YAMAMOTO, e., sorimahi, k., TAJIMA, e., WATANABE, h., SHIMIZU, h., proc. eurodisplay84, 9 th 1984: a210288 Matrix LCD Controlled by Double Stage diodes Rings, pages 141 and following, Paris: STROMER, M., Proc. Eurodiplacy 84, 9.1984: design of Thin Film Transistors for Matrix Addressing of Television Liquid Crystal display, page 145 and its succeeding pages, Paris ]. With decreasing resistance, the contrast of MLC displays degrades. The specific resistance of the liquid crystal mixture generally decreases over the lifetime of an MLC display due to interaction with the inner surfaces of the display, so a high (initial) resistance is very important for displays which must have an acceptable resistance value over a long operating time.
Thus, there is still a great need for MLC displays having very high specific resistance and at the same time a large operating temperature range, short response times and low threshold voltages, and it is desirable to be able to produce various gray levels with the aid of such displays.
The disadvantages of the MLC-TN displays which are generally used are due to their relatively low contrast, relatively high viewing angle dependence and the difficulty of producing gray levels in these displays.
VA displays have significantly better viewing angle dependence and are therefore used mainly for television sets and monitors. However, there is still a need to improve the response time here. At the same time, some properties such as low temperature stability and reliability must not be compromised. The liquid crystal material is also required to have good performance at low temperature, and particularly, the change of the driving voltage at low temperature relative to the driving voltage at normal temperature is required to be as small as possible.
The invention is based on the object of: a liquid crystal composition is provided which does not have or only to a reduced extent has the above-mentioned disadvantages. In particular, for monitors and televisions it must be ensured that they can operate even at very high and very low temperatures and at the same time have short response times and at the same time improved reliability characteristics, in particular no or significantly reduced image retention after long operating times.
Surprisingly, it is possible to improve the rotational viscosity values and thus the response times if one or more polar compounds according to formula I in the present application are used in liquid-crystalline compositions which are preferably used in VA displays, in particular in liquid-crystalline compositions having a negative dielectric anisotropy. Liquid-crystal mixtures, preferably VA, PS-VA, PSA, IPS and FFS mixtures, having short response times and at the same time good phase solubility properties and good low-temperature properties can be prepared by means of the compounds of the formula I.
Disclosure of Invention
The invention aims to provide a liquid crystal composition, and particularly relates to a liquid crystal composition with appropriate optical anisotropy, higher clearing point, larger negative dielectric anisotropy, low viscosity and high reliability, and a liquid crystal display device comprising the liquid crystal composition.
One aspect of the present invention provides a liquid crystal composition comprising:
at least one compound with a general formula I accounting for 1-20% of the total weight of the liquid crystal composition
Figure GDA0002662916930000041
Wherein the content of the first and second substances,
R1and R2The same or different, each independently represents an alkyl group or an alkoxy group having 1 to 7 carbon atoms, or an alkenyl group or an alkenyloxy group having 2 to 7 carbon atoms;
Figure GDA0002662916930000042
to represent
Figure GDA0002662916930000043
The above-mentioned
Figure GDA0002662916930000044
Upper arbitrary CH2May be substituted by O; the above-mentioned
Figure GDA0002662916930000045
Any of the above H may be substituted with F.
In some embodiments of the present invention, the liquid crystal composition may further comprise:
25-75% by weight of the total liquid crystal composition of at least one compound selected from the group consisting of formula II-1, II-2, II-3, II-4 and combinations thereof
Figure GDA0002662916930000046
And
Figure GDA0002662916930000047
wherein the content of the first and second substances,
R3、R5、R6、R7、R8、R9and R10The same or different, each independently represents an alkyl group or an alkoxy group having 1 to 7 carbon atoms, or an alkenyl group or an alkenyloxy group having 2 to 7 carbon atoms;
R4represents H, an alkyl group or an alkoxy group having 1 to 7 carbon atoms, or an alkenyl group or an alkenyloxy group having 2 to 7 carbon atoms.
In some embodiments of the present invention, the liquid crystal composition may further comprise:
20-70% by total weight of the liquid crystal composition of at least one compound selected from the group consisting of formula III-1, III-2, III-3, III-4, and combinations thereof
Figure GDA0002662916930000051
And
Figure GDA0002662916930000052
wherein the content of the first and second substances,
R11、R12、R13、R14、R15、R16、R17and R18The same or different, each independently represents an alkyl group or an alkoxy group having 1 to 7 carbon atoms, or an alkenyl group or an alkenyloxy group having 2 to 7 carbon atoms.
In some embodiments of the present invention, it is preferred that the at least one compound of formula I comprises from 1 to 20% by weight of the total liquid crystal composition; the at least one compound selected from the group consisting of formula II-1, formula II-2, formula II-3, formula II-4 and combinations thereof comprises 30-65% of the total weight of the liquid crystal composition; and the at least one compound selected from the group consisting of formulas III-1, III-2, III-3, III-4 and combinations thereof accounts for 30 to 60% of the total weight of the liquid crystal composition.
In some embodiments of the present invention, it is preferred that the compound of formula i is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000053
and
Figure GDA0002662916930000054
wherein the content of the first and second substances,
R1A、R2A、R1B、R2Bthe alkyl groups may be the same or different and each independently represents an alkyl group having 1 to 7 carbon atoms.
More preferably, the compound of formula I-1 is selected from one or more compounds from the group consisting of:
Figure GDA0002662916930000055
Figure GDA0002662916930000061
and
Figure GDA0002662916930000062
more preferably, the compound of formula I-2 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000063
Figure GDA0002662916930000071
and
Figure GDA0002662916930000072
in some embodiments of the present invention, it is preferred that the compound of formula II-1 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000073
Figure GDA0002662916930000081
and
Figure GDA0002662916930000082
in some embodiments of the present invention, it is preferred that the compound of formula II-2 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000083
and
Figure GDA0002662916930000091
in some embodiments of the present invention, it is preferred that the compound of formula II-3 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000092
and
Figure GDA0002662916930000093
in some embodiments of the present invention, it is preferred that the compound of formula II-4 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000094
and
Figure GDA0002662916930000095
in some embodiments of the present invention, it is preferred that the compound of formula III-1 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000101
and
Figure GDA0002662916930000102
in some embodiments of the present invention, it is preferred that the compound of formula III-2 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000103
Figure GDA0002662916930000111
and
Figure GDA0002662916930000112
in some embodiments of the present invention, it is preferred that the compound of formula III-3 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000113
Figure GDA0002662916930000121
Figure GDA0002662916930000131
and
Figure GDA0002662916930000132
in some embodiments of the present invention, it is preferred that the compound of formula III-4 is selected from one or more compounds of the group consisting of:
Figure GDA0002662916930000133
Figure GDA0002662916930000141
and
Figure GDA0002662916930000142
as a particularly preferred embodiment, said at least one compound of formula i represents from 3 to 18% of the total weight of said liquid crystal composition; the at least one compound selected from the group consisting of formula II-1, formula II-2, formula II-3, formula II-4 and combinations thereof comprises 30-64% of the total weight of the liquid crystal composition; and the at least one compound of the group of formulae III-1, III-2, III-3, III-4, and combinations thereof comprises 33 to 60% of the total weight of the liquid crystal composition.
The liquid crystal composition provided by the invention further comprises one or more additives known to those skilled in the art and described in the literature. For example, 0-15% pleochroic dyes and/or chiral dopants may be added.
The following shows possible dopants which are preferably added to the mixtures according to the invention.
Figure GDA0002662916930000143
Figure GDA0002662916930000151
Figure GDA0002662916930000152
And
Figure GDA0002662916930000153
in the embodiment of the present invention, it is preferable that the dopant accounts for 0 to 5% by weight of the total weight of the liquid crystal composition; more preferably, the dopant is present in an amount of 0 to 1% by weight based on the total weight of the liquid crystal composition.
The stabilizers which can be added to the liquid crystal composition according to the present invention are mentioned below.
Figure GDA0002662916930000161
Figure GDA0002662916930000171
Figure GDA0002662916930000181
Preferably, the stabilizer is selected from the group consisting of the stabilizers shown below:
Figure GDA0002662916930000182
in the embodiment of the present invention, it is preferable that the stabilizer accounts for 0 to 5% by weight of the total weight of the liquid crystal composition; more preferably, the stabilizer is 0-1% of the total weight of the liquid crystal composition; as a particularly preferred embodiment, the stabilizer is 0 to 0.1% by weight of the total weight of the liquid crystal composition.
In another aspect, the present invention provides a liquid crystal compound of the general formula I-2:
Figure GDA0002662916930000183
wherein the content of the first and second substances,
R1B、R2Bthe alkyl groups may be the same or different and each independently represents an alkyl group having 1 to 7 carbon atoms.
In some embodiments of the present invention, it is preferred that the compound of formula I-2 is selected from the group consisting of:
Figure GDA0002662916930000191
and
Figure GDA0002662916930000192
in another aspect, the present invention provides a process for the preparation of a compound of formula I-2:
Figure GDA0002662916930000201
the method comprises the following steps: in an organic solvent, performing suzuki coupling reaction on the iodide shown in the formula 1 and the boric acid compound shown in the formula 2 to obtain the compound shown in the general formula I-2.
In still another aspect, the present invention provides a liquid crystal display device comprising the liquid crystal composition of the present invention.
In still another aspect, the present invention provides a liquid crystal display device comprising the liquid crystal compound of the present invention.
The liquid crystal composition has proper optical anisotropy, higher clearing point, larger negative dielectric anisotropy, low viscosity and high reliability, is suitable for a liquid crystal display, and meets the requirement of quick response of the liquid crystal display.
In the present invention, unless otherwise specified, the proportions are weight ratios, all temperatures are in degrees centigrade, and the thickness of the box selected for the response time data test is 7 μm.
Detailed Description
The invention will be illustrated below with reference to specific embodiments. It should be noted that the following examples are illustrative of the present invention, and are not intended to limit the present invention. Other combinations and various modifications within the spirit or scope of the present invention may be made without departing from the spirit or scope of the present invention.
For convenience of expression, in the following examples, the group structure of the liquid crystal composition is represented by the code listed in Table 1:
TABLE 1 radical structural code of liquid crystal compounds
Figure GDA0002662916930000211
Compounds of the following formula are exemplified:
Figure GDA0002662916930000212
the structural formula is represented by the code listed in Table 1, and can be expressed as: nCPUF, where n in the code represents the number of C atoms in the left alkyl group, e.g., n is "3", i.e., the alkyl group is-C3H7(ii) a C in the code represents cyclohexane, P in the code represents 1, 4-phenylene, and U in the code represents 3, 5-difluoro-1, 4-phenylene.
The abbreviated codes of the test items in the following examples are as follows:
cp (. degree. C.): clearing points (nematic-isotropic phase transition temperature)
Δ n: optical anisotropy (589nm, 25 ℃ C.)
Δ ε: dielectric anisotropy (1KHz, 25 ℃ C.)
V (25 ℃ C.)/V (-20 ℃ C.): ratio of drive voltages at different temperatures
γ 1: torsional viscosity (mPas, 25 ℃ C.)
Wherein the refractive index anisotropy is measured by using an Abbe refractometer under a sodium lamp (589nm) light source at 20 ℃; the dielectric test cell was of the type TN90, the cell thickness being 7 μm.
Δ ∈ | ∈ | — |, where ∈ | is the dielectric constant parallel to the molecular axis and ∈ | is the dielectric constant perpendicular to the molecular axis, test conditions: at 25 ℃ and 1KHz, the test box is TN90 type, and the box thickness is 7 μm.
V (25 ℃): a drive voltage at 25 ℃; v (-20 ℃): -a drive voltage at 20 ℃.
Example 1
The liquid crystal composition of example 1 was prepared according to the compounds and weight percentages thereof listed in table 2, and filled between two substrates of a liquid crystal display for performance testing, and the test data are shown in the following table:
TABLE 2 liquid crystal composition formulations and their test properties
Figure GDA0002662916930000221
Example 2
The liquid crystal composition of example 2 was prepared according to the compounds and weight percentages thereof listed in table 3, and filled between two substrates of a liquid crystal display for performance testing, and the test data are shown in the following table:
TABLE 3 liquid crystal composition formula and its test performance
Figure GDA0002662916930000231
Example 3
The liquid crystal composition of example 3 was prepared according to the compounds and weight percentages thereof listed in table 4, and filled between two substrates of a liquid crystal display for performance testing, and the test data are shown in the following table:
TABLE 4 liquid crystal composition formula and its test performance
Figure GDA0002662916930000232
Example 4
The liquid crystal composition of example 4 was prepared according to the compounds and weight percentages thereof listed in table 5, and filled between two substrates of a liquid crystal display for performance testing, and the test data are shown in the following table:
TABLE 5 liquid crystal composition formulations and their test properties
Figure GDA0002662916930000241
As can be seen from the data of example 1, example 2, example 3 and example 4, the liquid crystal composition provided by the present invention has suitable optical anisotropy, a higher clearing point, a larger negative dielectric anisotropy, a low viscosity and high reliability, and can be applied to a liquid crystal display to meet the requirement of fast response of the liquid crystal display.
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 (9)

1. A liquid crystal composition, comprising:
at least one compound with a general formula I accounting for 1-20% of the total weight of the liquid crystal composition
Figure FDA0002809997640000011
30-65% by total weight of the liquid crystal composition of at least one compound selected from the group consisting of formula II-1, II-2, II-3, II-4 and combinations thereof
Figure FDA0002809997640000012
And
30-60% by total weight of the liquid crystal composition of at least one compound selected from the group consisting of formula III-1, III-2, III-3, III-4, and combinations thereof
Figure FDA0002809997640000013
And
Figure FDA0002809997640000014
wherein the content of the first and second substances,
R1and R2The same or different, each independently represents an alkyl group having 1 to 7 carbon atoms;
R3、R5、R6、R7、R8、R9、R10、R11、R12、R13、R14、R15、R16、R17and R18The same or different, each independently represents an alkyl group or an alkoxy group having 1 to 7 carbon atoms, or an alkenyl group or an alkenyloxy group having 2 to 7 carbon atoms;
R4represents H, an alkyl group or an alkoxy group having 1 to 7 carbon atoms, or an alkenyl group or an alkenyloxy group having 2 to 7 carbon atoms,
Figure FDA0002809997640000015
to represent
Figure FDA0002809997640000016
The above-mentioned
Figure FDA0002809997640000017
Any of the above H may be substituted with F.
2. The liquid crystal composition of claim 1, wherein the compound of formula i is selected from one or more compounds of the group consisting of:
Figure FDA0002809997640000021
and
Figure FDA0002809997640000022
wherein the content of the first and second substances,
R1A、R2A、R1B、R2Bthe alkyl groups may be the same or different and each independently represents an alkyl group having 1 to 7 carbon atoms.
3. The liquid crystal composition according to claim 2, wherein the compound of formula i-1 is selected from one or more compounds selected from the group consisting of:
Figure FDA0002809997640000023
Figure FDA0002809997640000031
and
Figure FDA0002809997640000032
and is
The compound of the general formula I-2 is selected from one or more compounds of the group consisting of:
Figure FDA0002809997640000033
Figure FDA0002809997640000041
and
Figure FDA0002809997640000042
4. the liquid crystal composition according to claim 1, wherein the compound of formula ii-1 is one or more compounds selected from the group consisting of:
Figure FDA0002809997640000043
and
Figure FDA0002809997640000044
the compound of the general formula II-2 is selected from one or more compounds of the group consisting of:
Figure FDA0002809997640000045
Figure FDA0002809997640000051
and
Figure FDA0002809997640000052
the compound of the general formula II-3 is one or more compounds selected from the group consisting of:
Figure FDA0002809997640000053
and
Figure FDA0002809997640000054
and is
The compound of formula II-4 is selected from one or more compounds of the group consisting of:
Figure FDA0002809997640000055
Figure FDA0002809997640000061
and
Figure FDA0002809997640000062
5. the liquid crystal composition according to claim 1, wherein the compound of formula iii-1 is selected from one or more compounds from the group consisting of:
Figure FDA0002809997640000063
and
Figure FDA0002809997640000064
the compound of the general formula III-2 is selected from one or more compounds of the group consisting of:
Figure FDA0002809997640000071
and
Figure FDA0002809997640000072
the compound of the general formula III-3 is selected from one or more compounds from the group consisting of:
Figure FDA0002809997640000073
Figure FDA0002809997640000081
Figure FDA0002809997640000091
and
Figure FDA0002809997640000092
and is
The compound of the general formula III-4 is selected from one or more compounds from the group consisting of:
Figure FDA0002809997640000093
Figure FDA0002809997640000101
and
Figure FDA0002809997640000102
6. the liquid crystal composition of claim 1, wherein the at least one compound of formula i comprises from 3 to 18% by weight of the total liquid crystal composition; the at least one compound selected from the group consisting of formula II-1, formula II-2, formula II-3, formula II-4 and combinations thereof comprises 30-64% of the total weight of the liquid crystal composition; and the at least one compound of the group of formulae III-1, III-2, III-3, III-4, and combinations thereof comprises 33 to 60% of the total weight of the liquid crystal composition.
7. The liquid crystal composition of claim 6, wherein the liquid crystal composition comprises, based on the total weight of the liquid crystal composition:
18% of compound
Figure FDA0002809997640000103
8% of a compound
Figure FDA0002809997640000111
10% of a compound
Figure FDA0002809997640000112
11% of a compound
Figure FDA0002809997640000113
10% of a compound
Figure FDA0002809997640000114
12% of a compound
Figure FDA0002809997640000115
7% of a compound
Figure FDA0002809997640000116
6% of a compound
Figure FDA0002809997640000117
3% of a compound
Figure FDA0002809997640000118
3% of a compound
Figure FDA0002809997640000119
2% of a compound
Figure FDA00028099976400001110
5% of a compound
Figure FDA00028099976400001111
And
5% of a compound
Figure FDA00028099976400001112
Alternatively, the liquid crystal composition comprises, based on the total weight of the liquid crystal composition:
20% of the compound
Figure FDA00028099976400001113
5% of a compound
Figure FDA00028099976400001114
10% of a compound
Figure FDA00028099976400001115
11% of a compound
Figure FDA00028099976400001116
8% of a compound
Figure FDA00028099976400001117
10% of a compound
Figure FDA00028099976400001118
6% of a compound
Figure FDA00028099976400001119
6% of a compound
Figure FDA0002809997640000121
3% of a compound
Figure FDA0002809997640000122
3% of a compound
Figure FDA0002809997640000123
6% of a compound
Figure FDA0002809997640000124
6% of a compound
Figure FDA0002809997640000125
And
6% of a compound
Figure FDA0002809997640000126
Alternatively, the liquid crystal composition comprises, based on the total weight of the liquid crystal composition:
35% of a compound
Figure FDA0002809997640000127
8% of a compound
Figure FDA0002809997640000128
5% of a compound
Figure FDA0002809997640000129
7% of a compound
Figure FDA00028099976400001210
7% of a compound
Figure FDA00028099976400001211
6% of a compound
Figure FDA00028099976400001212
6% of a compound
Figure FDA00028099976400001213
2% of a compound
Figure FDA00028099976400001214
12% of a compound
Figure FDA00028099976400001215
4% of a compound
Figure FDA00028099976400001216
4% of a compound
Figure FDA00028099976400001217
And
4% of a compound
Figure FDA00028099976400001218
Alternatively, the liquid crystal composition comprises, based on the total weight of the liquid crystal composition:
15% of the compound
Figure FDA0002809997640000131
15% of the compound
Figure FDA0002809997640000132
10% of a compound
Figure FDA0002809997640000133
5% of a compound
Figure FDA0002809997640000134
3% of a compound
Figure FDA0002809997640000135
7% of a compound
Figure FDA0002809997640000136
6% of a compound
Figure FDA0002809997640000137
6% of a compound
Figure FDA0002809997640000138
6% of a compound
Figure FDA0002809997640000139
12% of a compound
Figure FDA00028099976400001310
12% of a compound
Figure FDA00028099976400001311
And
3% of a compound
Figure FDA00028099976400001312
8. The liquid crystal composition of claim 1, further comprising one or more additives.
9. A liquid crystal display device comprising the liquid crystal composition of any one of claims 1-8.
CN201610825423.6A 2016-09-14 2016-09-14 Liquid crystal compound, liquid crystal composition and display device Active CN107815322B (en)

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