Liquid crystal composition, liquid crystal display element and liquid crystal display

Abstract

A liquid crystal composition, a liquid crystal display element and a liquid crystal display comprising the liquid crystal composition belong to the field of liquid crystal display. The liquid crystal composition of the present disclosure comprises a compound represented by formula I, a compound represented by formula II, one or more compounds represented by formula III, one or more compounds represented by formula IV and more than three compounds represented by formula V. The liquid crystal composition has low rotational viscosity γ1 and high stability to heat and light on the basis of maintaining appropriate optical anisotropy Δn, which can realize fast response of liquid crystal display. ##STR00001##

Claims

1. A liquid crystal composition, wherein the liquid crystal composition comprises a compound represented by formula I, a compound represented by formula II, a compound represented by formula III-2, a compound represented by formula IV-10, three different compounds represented by formula V, a compound represented by formula VI-4, a compound represented by formula VII-10, a compound represented by formula VII-12, and one or more compounds represented by formula VIII except for those represented by formula I and II: ##STR00046## wherein, R.sub.5 represents alkyl group having a carbon atom number of 1-10; R.sub.6 represents alkoxy group having a carbon atom number of 1-2; Z.sub.1 represents a single bond; n represents 1 or 2; when n represents 1, ##STR00047## represents 1,4-Phenylene, or 1,4-cyclohexylidene; when n represents 2, two ##STR00048## independently represents 1,4-cyclohexylidene; R.sub.91 and R.sub.101 independently represent alkyl groups with 2-5 carbon atoms; R.sub.11 represents alkyl group having a carbon atom number of 3-4; R.sub.12 represents alkyl group having a carbon atom number of 1-10 or alkenyl group having a carbon atom number of 2-10; ##STR00049## independently represent 1,4-cyclohexylidene; a total mass content of the compound represented by formula I is 15%, a total mass content of the compound represented by formula II is 6.5-13.5%, a total mass content of the compound represented by formula III-2 is 12%, a total mass content of the compound represented by formula IV-10 is 8%, a total mass content of the compounds represented by formula V is 24.5%, a total mass content of the compound represented by formula VI-4 is 16%, a total mass content of the compounds represented by formula VII-10 and formula VII-12 is 7%, a total mass content of the compounds represented by formula VIII is 4-11%.

2. The liquid crystal composition according to claim 1, wherein that the compounds represented by formula V are selected from the group consisting of compounds of V-1, V-2 and V-7: ##STR00050## wherein, R.sub.5 represents alkyl group having a carbon atom number of 3.

3. The liquid crystal composition according to claim 1, wherein that the liquid crystal composition also comprises one or more compounds represented by formula IX: ##STR00051## wherein, R.sub.13 and R.sub.14 independently represent alkyl group having a carbon atom number of 1-10, fluoro-substituted alkyl group having a carbon atom number of 1-10, alkoxy group having a carbon atom number of 1-10, fluoro-substituted alkoxy group having a carbon atom number of 1-10, alkenyl group having a carbon atom number of 2-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, alkenoxy group having a carbon atom number of 3-8 or fluoro-substituted alkenoxy group having a carbon atom number of 3-8; X.sub.1, X.sub.2, and X.sub.3 independently represent H or F.

4. A liquid crystal display element or liquid crystal display, comprising the liquid crystal composition according to claim 1, said liquid crystal display element or liquid crystal display being an active matrix addressing display element or display, or a passive matrix addressing display element or display.

Description

DETAILED DESCRIPTION OF EMBODIMENTS

(1) [Liquid Crystal Composition]

(2) The liquid crystal composition of the present disclosure comprises a compound represented by formula I, a compound represented by formula II, one or more compounds represented by formula III, one or more compounds represented by formula IV, and more than three compounds represented by formula V:

(3) ##STR00005##

(4) wherein,

(5) R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 independently represent alkyl group having a carbon atom number of 1-10, fluoro-substituted alkyl group having a carbon atom number of 1-10, alkoxy group having a carbon atom number of 1-10, fluoro-substituted alkoxy group having a carbon atom number of 1-10, alkenyl group having a carbon atom number of 2-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, alkenoxy group having a carbon atom number of 3-8 or fluoro-substituted alkenoxy group having a carbon atom number of 3-8;

(6) and, any one —CH.sub.2— or several —CH.sub.2— that are not adjacent in the groups indicated by R.sub.1, R.sub.3 and R.sub.5 are selectively substituted by cyclopentyl, cyclobutyl or cyclopropyl;

(7) Z.sub.1 represents a single bond, —CH.sub.2CH.sub.2— or —CH.sub.2O—;

(8) n represents 0, 1 or 2;

(9) when n represents 1,

(10) ##STR00006##
represents 1,4-Phenylene, 1,4-cyclohexylidene or 1,4-cyclohexene;

(11) when n represents 2,

(12) ##STR00007##
independently represent 1,4-Phenylene or 1,4-cyclohexylidene.

(13) The liquid crystal composition of the present disclosure has low rotational viscosity and high thermal and light stability on the basis of maintaining appropriate optical anisotropy Δn.

(14) For example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert butyl, n-amyl, isoamyl, hexyl, heptyl, octyl, nonyl, decyl, etc. can be listed as the alkyl groups with carbon atom number of 1-10.

(15) For example, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, pentoxy, hexoxy, hepthoxy, octyloxy, nonoxy, decaoxy, etc. can be listed as the alkoxy groups with the carbon atom number of 1˜10.

(16) For example, vinyl, 1-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-Pentenyl, 1-hexenyl, 2-hexenyl, 3-Hexenyl, etc., can be listed as alkenyl groups with carbon atom number of 2˜10.

(17) The “fluoro-substituted” in the fluoro-substituted alkyl group having a carbon atom number of 1-10, fluoro-substituted alkoxy group with the carbon atom number of 1-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, and fluoro-substituted alkenoxy group having a carbon atom number of 3-8 can be single fluorine substitution, or multi fluorine substitution, such as difluoro substitution and trifluoro substitution, or perfluoro substitution. There is no special algebra for fluorine limitation. For example, fluoromethyl, difluoromethyl, trifluoromethyl, 1-fluoroethyl, 2-fluoroethyl, 1,2-difluoroethyl, 1,1,2-trifluoroethyl, 1,1,2-trifluoroethyl, 1,1,2-trifluoroethyl, 1,1,1,2,2-pentafluoroethyl, etc. can be listed, but not limited to.

(18) In the liquid crystal composition of the present disclosure, there is no special restriction on the content of the compounds of the formula I, II, III and IV as the composition thereof. In a preferred embodiment, the total mass content of the compounds represented by formula I and formula II is 20-50%, the total mass content of the compound represented by formula III is 1-15%, the total mass content of the compound represented by formula IV is 1-20%, and the total mass content of the compound represented by formula V is 1-40%.

(19) In the liquid crystal composition of the present disclosure, the compound represented by formula III is preferably selected from the group consisting of compounds represented by formula III-1 to III-12:

(20) ##STR00008## ##STR00009##

(21) In the liquid crystal composition of the present disclosure, the compounds represented by formula IV are preferably consisting of compounds from formula IV-1 to IV-15:

(22) ##STR00010## ##STR00011##

(23) In the liquid crystal composition of the present disclosure, the compounds represented by formula V are preferably selected from the group consisting of compounds of V-1 to V-8:

(24) ##STR00012##

(25) wherein, R.sub.5 and R.sub.6 independently represent alkyl group having a carbon atom number of 1-10, fluoro-substituted alkyl group having a carbon atom number of 1-10, alkoxy group having a carbon atom number of 1-10, fluoro-substituted alkoxy group having a carbon atom number of 1-10, alkenyl group having a carbon atom number of 2-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, alkenoxy group having a carbon atom number of 3-8 or fluoro-substituted alkenoxy group having a carbon atom number of 3-8;

(26) and, any one —CH.sub.2— or several —CH.sub.2— that are not adjacent in R.sub.5 group is selectively substituted by cyclopentyl, cyclobutyl or cyclopropyl.

(27) In one embodiment of the liquid crystal composition, preferably, the liquid crystal composition also comprises one or more compounds represented by formula VI:

(28) ##STR00013##

(29) wherein,

(30) R.sub.7 and R.sub.8 independently represent alkyl group having a carbon atom number of 1-10, fluoro-substituted alkyl group having a carbon atom number of 1-10, alkoxy group having a carbon atom number of 1-10, fluoro-substituted alkoxy group having a carbon atom number of 1-10, alkenyl group having a carbon atom number of 2-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, alkenoxy group having a carbon atom number of 3-8 or fluoro-substituted alkenoxy group having a carbon atom number of 3-8;

(31) ##STR00014##
independently represent 1,4-Phenylene, 1,4-cyclohexylidene or 1,4-cyclohexene.

(32) By combining the compounds represented by formula VI in the liquid crystal composition of the present disclosure, the optical anisotropy of the liquid crystal composition can be increased and the clear point of the liquid crystal composition can be improved.

(33) In one embodiment of the liquid crystal composition of the present disclosure, preferably, the compound represented by formula VI is preferably consisting of compounds from formula VI-1 to VI-7:

(34) ##STR00015##

(35) In another embodiment of the liquid crystal composition disclosed, preferably, the liquid crystal composition further comprises one or more compounds represented by formula VII:

(36) ##STR00016##

(37) wherein,

(38) R.sub.9 and R.sub.10 independently represent alkyl group having a carbon atom number of 1-10, fluoro-substituted alkyl group having a carbon atom number of 1-10, alkoxy group having a carbon atom number of 1-10, fluoro-substituted alkoxy group having a carbon atom number of 1-10, alkenyl group having a carbon atom number of 2-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, alkenoxy group having a carbon atom number of 3-8 or fluoro-substituted alkenoxy group having a carbon atom number of 3-8, any one —CH.sub.2— or several —CH.sub.2— that are not adjacent in the groups indicated by R.sub.9 and R.sub.10 are selectively substituted by cyclopentyl, cyclobutyl or cyclopropyl;

(39) X represents —O—, —S— or —CH.sub.2O—.

(40) By using the compound represented by formula VII in the liquid crystal composition of the present disclosure, the liquid crystal composition can have large negative dielectric anisotropy, which is conducive to reducing the driving voltage of the device.

(41) In another embodiment of the liquid crystal composition of the present disclosure, it is preferred that the compounds represented by formula VII are selected from the group consisting of the compounds represented by formulas VII-1 to VII-12:

(42) ##STR00017## ##STR00018##

(43) wherein, R.sub.91 and R.sub.101 independently represent alkyl groups with 1-10 carbon atoms.

(44) In a further embodiment of the liquid crystal composition of the invention, it is preferred that the liquid crystal composition also comprises one or more compounds represented by formula VIII except for those represented by formula I and II:

(45) ##STR00019##

(46) R.sub.11 and R.sub.12 independently represent alkyl group having a carbon atom number of 1-10, fluoro-substituted alkyl group having a carbon atom number of 1-10, alkoxy group having a carbon atom number of 1-10, fluoro-substituted alkoxy group having a carbon atom number of 1-10, alkenyl group having a carbon atom number of 2-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, alkenoxy group having a carbon atom number of 3-8 or fluoro-substituted alkenoxy group having a carbon atom number of 3-8;

(47) ##STR00020##
independently represent 1,4-Phenylene, 1,4-cyclohexylidene or 1,4-cyclohexene.

(48) By containing the compound represented by formula VIII in the liquid crystal composition of the present disclosure, the mutual solubility of the liquid crystal composition can be improved, the rotational viscosity can be reduced, and the response speed of the liquid crystal composition of the present disclosure can be improved.

(49) In another embodiment of the liquid crystal composition of the present disclosure, it is preferred that the compounds represented by formula VIII are selected from the group consisting of compounds represented by formulas VIII-1 to VIII-9:

(50) ##STR00021##

(51) In another embodiment of the liquid crystal composition disclosed, preferably, the liquid crystal composition further comprises one or more compounds represented by formula IX:

(52) ##STR00022##

(53) wherein,

(54) R.sub.13 and R.sub.14 independently represent alkyl group having a carbon atom number of 1-10, fluoro-substituted alkyl group having a carbon atom number of 1-10, alkoxy group having a carbon atom number of 1-10, fluoro-substituted alkoxy group having a carbon atom number of 1-10, alkenyl group having a carbon atom number of 2-10, fluoro-substituted alkenyl group having a carbon atom number of 2-10, alkenoxy group having a carbon atom number of 3-8 or fluoro-substituted alkenoxy group having a carbon atom number of 3-8;

(55) X.sub.1, X.sub.2, X.sub.3 independently represent H or F.

(56) By containing the compound represented by formula IX in the liquid crystal composition of the present disclosure, the brightness point of the liquid crystal composition can be improved.

(57) In another embodiment of the liquid crystal composition of the present disclosure, it is preferred that the compounds represented by formula IX are selected from the group consisting of the compounds represented by formulas IX-1 to IX-5:

(58) ##STR00023##

(59) Various functional dopants can also be added to the liquid crystal compound of the present disclosure, and the dopant content is preferably between 0.01% and 1%. These dopants can be listed as antioxidants, ultraviolet absorbents and chiral agents.

(60) Antioxidants, UV absorbers may be preferably listed as follows:

(61) ##STR00024##

(62) S represents an integer from 1 to 10.

(63) Chiral agents (left-handed or right-handed) are preferred can be listed as follows:

(64) ##STR00025##

(65) The present disclosure also relates to a liquid crystal display element or a liquid crystal display comprising any one of the above liquid crystal compositions; the display element or display is an active matrix display element or display or a passive matrix display element or display.

(66) The liquid crystal display element or liquid crystal display of the present disclosure preferably adopts active matrix addressing liquid crystal display element or liquid crystal display.

(67) The above-mentioned active matrix display elements or displays can specifically list TN-TFT or IPS-TFT or VA-TFT liquid crystal display elements or other TFT displays.

(68) The liquid crystal composition provided by the present disclosure has low rotational viscosity γ.sub.1 and high thermal and light stability on the basis of maintaining appropriate optical anisotropy Δn.

(69) [Liquid Crystal Display Element or Liquid Crystal Display]

(70) The liquid crystal display element or liquid crystal display of the present disclosure comprises a liquid crystal composition of the present disclosure. The liquid crystal display element or liquid crystal display of the present disclosure has a wide nematic temperature range, suitable birefringence anisotropy, very high resistivity, good ultraviolet resistance and fast response time, and can be widely used in 4K and 8K displays.

EMBODIMENTS

(71) In order to explain the present disclosure more clearly, the present disclosure will be further explained in combination with the embodiment. Those skilled in the art should understand that the contents described below are illustrative rather than restrictive, and the scope of protection of the present disclosure should not be limited.

(72) In this manual, unless otherwise specified, the percentage refers to the mass percentage, and the temperature is degree centigrade (° C.). The specific meaning and test conditions of other symbols are as follows:

(73) Cp is the clear point of liquid crystal (° C.), which is measured by DSC quantitative method;

(74) Δn is the optical anisotropy, n.sub.o is the refractive index of ordinary light, n.sub.e is the refractive index of extraordinary light, the test conditions are 25±2° C., 589 nm, Abbe refractometer test;

(75) Δε is the dielectric anisotropy, Δε=ε.sub.∥−ε.sub.⊥, where ε.sub.∥ is the dielectric constant parallel to the molecular axis, and ε.sub.⊥ is the dielectric constant perpendicular to the molecular axis. The test conditions are 25±0.5° C., 20 um vertical box, INSTEC:ALCT-IR1 testing;

(76) γ.sub.1 is the rotational viscosity (mPa.Math.s), and the test conditions are 25±0.5° C. and 20 um vertical box, INSTEC:ALCT-IR1 testing;

(77) K.sub.11 is the torsional elastic constant and K.sub.33 is the unfolding elastic constant INSTEC:ALCT-IR1, 20 um vertical box;

(78) VHR is the voltage retention rate (%), the test condition is 60±1° C., the voltage is ±5V, the pulse width is 10 ms, and the voltage holding time is 1.667 ms. The test equipment is TOYO Model6254 liquid crystal performance comprehensive tester;

(79) The preparation method of the liquid crystal composition is as follows: each liquid crystal monomer is weighed according to a certain proportion and put into a stainless steel beaker; the stainless steel beaker containing each liquid crystal monomer is heated and melted on the magnetic stirring instrument; after most of the liquid crystal monomer in the stainless steel beaker is melted, a magnetic rotor is added into the stainless steel beaker, and the mixture is stirred evenly and cooled to room temperature to obtain liquid crystal composition.

(80) The structure of liquid crystal monomer in the embodiment of the disclosure is represented by codes. The codes for ring structures, end groups and linking groups of liquid crystals are represented as in Tables 1 and 2 below.

(81) TABLE-US-00001 TABLE 1 Corresponding codes for ring structure Ring structure Corresponding code C P L G 0 Gi Y Sb Sc

(82) TABLE-US-00002 TABLE 2 Corresponding codes of end group and linking group End group and linking group Corresponding code C.sub.nH.sub.2n+1— n- C.sub.nH.sub.2n+1O— nO— —CF.sub.3 —T —OCF.sub.3 —OT —CH.sub.2O— —O— —F —F —CH.sub.2CH.sub.2— —E— —CH═CH— —V— —CH═CH—C.sub.nH.sub.2n+1 Vn- Cp- Cpr- Cpr1- CpO CprO

EXAMPLES

(83) ##STR00039##
the code is CPY-2-O2;

(84) ##STR00040##
the code is CCY-3-O2;

(85) ##STR00041##
the code is COY-3-O2;

(86) ##STR00042##
the code is CCOY-3-O2;

(87) ##STR00043##
the code is Sb-CpO-O4;

(88) ##STR00044##
the code is Sc-CpO-O4.

Example 1

(89) The formula and corresponding properties of the liquid crystal composition are as shown in table 3.

(90) TABLE-US-00003 TABLE 3 Formula and corresponding properties of liquid crystal composition of example 1 Category Liquid crystal monomer code Content (%) I CC-3-V 15 II CC-2-3 6.5 III CLY-3-O2 12 IV PYP-2-3 8 V CY-3-O2 8.5 V PY-3-O2 11.5 V CCY-3-O1 4.5 VI CCP-3-1 16 VII Sc-2O-O5 3 VII Sb-2O-O5 4 VIII CC-3-V1 7 VIII CC-4-3 4 Δε[1 KHz, 25° C.]: −3.0 Δn[589 nm, 25° C.]: 0.105 K.sub.11: 13.5 K.sub.33: 15.8 Cp: 81° C. γ.sub.1: 77 mPa .Math. s

Comparative Example 1

(91) The formula and corresponding properties of the liquid crystal composition are as shown in table 4 below.

(92) TABLE-US-00004 TABLE 4 Formula and corresponding properties of liquid crystal composition with Comparative Example 1 Category Liquid crystal monomer code Content (%) I CC-3-V 15 II CC-2-3 6.5 V CCY-3-O2 12 IV PYP-2-3 8 V CY-3-O2 8.5 V PY-3-O2 11.5 V CCY-3-O1 4.5 VI CCP-3-1 16 VII Sc-2O-O5 3 VII Sb-2O-O5 4 VIII CC-3-V1 7 VIII CC-4-3 4 Δε[1 KHz, 25° C.]: −3.0 Δn[589 nm, 25° C.]: 0.103 K.sub.11: 13.1 K.sub.33: 15.5 Cp: 80° C. γ.sub.1: 82 mPa .Math. s

(93) For Comparative Example 1, CLY-3-O2 in Example 1 is replaced with CCY-3-O2, and the rest is the same as that of Example 1. Compared with the Comparative Example 1, γ.sub.1 in Example 1 of the present disclosure is significantly reduced, and the response speed of the liquid crystal display can be improved.

Example 2

(94) The formula and corresponding properties of the liquid crystal composition are as shown in table 5.

(95) TABLE-US-00005 TABLE 5 Formula and corresponding properties of liquid crystal composition of example 2 Category Liquid crystal monomer code Content (%) I CC-3-V 15 II CC-2-3 13.5 III CLY-3-O2 12 IV PYP-2-3 8 V PY-3-O2 11.5 V CCY-3-O1 4.5 V CY-3-O2 8.5 VI CCP-3-1 16 VII Sc-2O-O5 3 VII Sb-2O-O5 4 VIII CC-4-3 4 Δε[1 KHz, 25° C.]: −3.1 Δn[589 nm, 25° C.]: 0.106 Cp: 72° C. K.sub.11: 12.3 K.sub.33: 13.3 γ.sub.1: 63 mPa .Math. s

Comparative Example 2

(96) The formula and corresponding properties of the liquid crystal composition are as shown in table 6.

(97) TABLE-US-00006 TABLE 6 Formula and performance of liquid crystal composition with Comparative Example 2 Category Liquid crystal monomer code Content (%) I CC-3-V 15 VIII CC-V-V 13 V CCY-3-O2 12 IV PYP-2-3 8 V CY-3-O2 8 V PY-3-O2 12 V CPY-3-O2 7 VI CCP-3-1 10 VII Sc-2O-O5 3 VII Sb-2O-O5 4 Δε[1 KHz, 25° C.]: −3.0 Δn[589 nm, 25° C.]: 0.105 Cp: 73° C. K.sub.11: 12.0 K.sub.33: 14.0 γ.sub.1: 71 mPa .Math. s

(98) CLY-3-O2 was replaced with CCY-3-O2 and CC-2-3 was replaced with CC-V-V in example 2, and the rest were the same as those in example 2, as the corresponding Comparative Example 2. Compared with the Comparative Example 2, the γ.sub.1 in the example 2 of the present disclosure is decreased.

(99) TABLE-US-00007 TABLE 7 VHR control values of Example 2 and Comparative Example 2 VHR high Experiment VHR initial VHR UV temperature number (60° C., 0.6 Hz) (60° C., 0.6 Hz) (60° C., 0.6 Hz) Example 2 76.5% 86.2% 95.2% Comparative 72.2% 84.5% 94.3% Example 2

(100) The reliability of liquid crystal composition is tested by UV, high temperature aging test and VHR test. The smaller the change of VHR data before and after UV and high temperature test, the stronger the ability of anti ultraviolet and high temperature. Therefore, the ability of anti ultraviolet and high temperature resistance is judged by comparing the difference of VHR data of each example and comparison case before and after the test.

(101) In the above experiment, the liquid crystal of the example and the comparative example liquid crystal are respectively poured into the test piece for testing. The VHR represents the voltage retention rate (%), the test conditions are 60±1° C., the voltage is ±5V, the pulse width is 10 ms, and the voltage holding time is 1.667 ms; the test equipment is TOYO Model6254 liquid crystal performance comprehensive tester; the initial value of VHR is the data obtained by testing the test piece without any treatment. The VHR ultraviolet is the VHR value obtained by irradiating the liquid crystal film filled with liquid crystal under normal temperature ultraviolet light for 5000 mj, and the VHR high temperature aging is the VHR value obtained by testing the liquid crystal filled sheet in the high temperature oven at 100° C. for 1 hour. Compared with the corresponding Comparative Example 2, the VHR ultraviolet and VHR high temperature aging values of example 2 are higher than those of the corresponding Comparative Example VHR, especially the VHR ultraviolet value measured after ultraviolet irradiation is significantly higher than that of the corresponding Comparative Example 2, indicating that the liquid crystal composition of example 2 has stronger anti ultraviolet and high temperature resistance than Comparative Example 2, so that the ability of resisting external environmental damage in the working process is also stronger than that of Comparative Example 2, more reliable.

Example 3

(102) The formula and corresponding properties of the liquid crystal composition are as shown in table 8.

(103) TABLE-US-00008 TABLE 8 Formula and corresponding properties of liquid crystal composition of example 3 Category Liquid crystal monomer code Content (%) I CC-3-V 34.5 II CC-2-3 8 III CLY-3-O2 6 IV PYP-Cpr-2 3 V CPY-3-O2 11.5 V CCOY-3-O2 3.5 V PY-3-O2 16 V CCY-3-O2 11.5 VII Sb-1O-O4 3 VII Sc-1O-O4 3 Δε[1 KHz, 25° C.]: −3.7 Δn[589 nm, 25° C.]: 0.105 Cp: 78° C. K.sub.11: 11.9 K.sub.33: 14.6 γ.sub.1: 77 mPa .Math. s

Example 4

(104) The formula and corresponding properties of the liquid crystal composition are as shown in table 9 below.

(105) TABLE-US-00009 TABLE 9 Formula and corresponding properties of liquid crystal composition of example 4 Category Liquid crystal monomer code Content (%) I CC-3-V 34.5 II CC-2-3 8 III CLY-3-O2 10 IV PYP-Cpr-2 3 V CPY-3-O2 11.5 V CCOY-3-O2 7.5 V PY-3-O2 16 VII Sb-1O-O4 3 VII Sc-1O-O4 3 Δε[1 KHz, 25° C.]: −3.8 Δn[589 nm, 25° C.]: 0.102 Cp: 70° C. K.sub.11: 11.7 K.sub.33: 13.8 γ.sub.1: 67 mPa .Math. s

Example 5

(106) The formula and corresponding properties of the liquid crystal composition are as shown in table 10 below.

(107) TABLE-US-00010 TABLE 10 Formula and corresponding properties of liquid crystal composition of example 5 Category Liquid crystal monomer code Content (%) I CC-3-V 29.5 II CC-2-3 20 III CLY-3-O2 10 IV PYP-Cpr-2 8 V CPY-3-O2 11.5 V PY-3-O2 12 V CPY-2-O2 6 VII Sc-2O-O4 3 Δε[1 KHz, 25° C.]: −3.0 Δn[589 nm, 25° C.]: 0.103 K.sub.11: 11.7 K.sub.33: 13.2 Cp: 70° C. γ.sub.1: 61 mPa .Math. s

Example 6

(108) The formula and corresponding properties of the liquid crystal composition are as shown in table 11 below.

(109) TABLE-US-00011 TABLE 11 Formula and corresponding properties of liquid crystal composition of example 6 Content Category Liquid crystal monomer code (%) I CC-3-V 29.5 II CC-2-3 20 III CLY-3-O2 10 IV PYP-Cpr-2 2 V CY-3-O2 3 V CCY-3-O2 5 V PY-3-O2 12 V CPY-3-O2 11.5 IX CCP-3-2 4 VII Sc-1O-O4 3 0.03 Δε[1 KHz, 25° C.]: −2.8 Δn[589 nm, 25° C.]: 0.103 K.sub.11: 11.9 K.sub.33: 13.5 Cp: 75° C. γ.sub.1: 74 mPa•s

Example 7

(110) The formula and corresponding properties of the liquid crystal composition are as shown in table 12.

(111) TABLE-US-00012 TABLE 12 Formula and corresponding properties of liquid crystal composition of example 7 Category Liquid crystal monomer code Content (%) I CC-3-V 29.5 II CC-2-3 7 III CLY-3-O2 10 IV PYP-Cpr-2 4 V CCOY-3-O2 6 V CPY-2-O2 7 V PY-3-O2 16.5 V COY-3-O2 4 VI CPP-3-2V1 10 VII Sc-1O-O4 3 VIII CC-4-3 3 Δε[1 KHz, 25° C.]: −3.0 Δn[589 nm, 25° C.]: 0.109 K.sub.11: 12.2 K.sub.33: 14.4 Cp: 75° C. γ.sub.1: 77 mPa .Math. s

Example 8

(112) The formula and corresponding properties of the liquid crystal composition are as shown in table 13 below.

(113) TABLE-US-00013 TABLE 13 Formula and corresponding properties of liquid crystal composition of example 8 Category Liquid crystal monomer code Content (%) I CC-3-V 29 II CC-2-3 7 III CLY-3-O2 10 IV PYP-Cpr-2 4 V PY-3-O2 17 V CCOY-3-O2 10 V CPY-2-O2 7 VI CPP-3-2V1 10 VII Sb-2O-O4 3 VIII CP-3-O2 3 Δε[1 KHz, 25° C.]: −3.2 Δn[589 nm, 25° C.]: 0.111 K.sub.11: 13.1 K.sub.33: 14.5 Cp: 80° C. γ.sub.1: 80 mPa .Math. s

Example 9

(114) The formula and corresponding properties of the liquid crystal composition are as shown in table 14 below.

(115) TABLE-US-00014 TABLE 14 Formula and corresponding properties of liquid crystal composition of example 9 Category Liquid crystal monomer code Content (%) I CC-3-V 24.5 II CC-2-3 7 III CLY-3-O2 10 IV PYP-Cpr-2 4 V CCOY-3-O2 10 V PY-3-O2 17 V CPY-2-O2 7 VI CPP-3-2V1 10 VIII PP-5-1 7 VII Sb-1O-O4 3 Δε[1 KHz, 25° C.]: −3.2 Δn[589 nm, 25° C.]: 0.118 K.sub.11: 14.5 K.sub.33: 13.9 Cp: 75° C. γ.sub.1: 74 mPa .Math. s

Example 10

(116) The formula and corresponding properties of the liquid crystal composition are as shown in table 15 below.

(117) TABLE-US-00015 TABLE 15 Formula and corresponding properties of liquid crystal composition of example 10 Category Liquid crystal monomer code Content (%) I CC-3-V 24.5 II CC-2-3 7 III CLY-3-O2 10 IV PYP-Cpr-2 4 V CY-3-O2 17 V CCOY-2-O2 6 V CCOY-3-O2 11 VI CCP-3-O1 3.5 VI CPP-3-2V1 10 VII Sb-1O-O4 3 IX CGPC-3-3 4 Δε[1 KHz, 25° C.]: −3.4 Δn[589 nm, 25° C.]: 0.101 K.sub.11: 15.9 K.sub.33: 16.5 Cp: 98° C. γ.sub.1: 108 mPa .Math. s

(118) Obviously, the above-mentioned examples of the present disclosure are only for the purpose of clearly explaining the examples of the present disclosure, rather than limiting the implementation mode of the present disclosure. For ordinary technical personnel in the art, other changes or changes in different forms can be made on the basis of the above description. Here, it is impossible to enumerate all the examples, and all the technologies belong to the present disclosure The obvious changes or changes in the technical scheme are still within the scope of protection of the present disclosure.