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

Abstract

A liquid crystal composition, and a liquid crystal display element or liquid crystal display including the liquid crystal composition and belonging to the field of liquid crystal display. The liquid crystal composition includes a compound represented by formula I, a compound represented by formula II, one or more compounds represented by formula III, and at least one polymerizable compound. The liquid crystal composition simultaneously has a low rotary viscosity, a large refractive index, and a fast response speed. ##STR00001##

Claims

1. A liquid crystal composition, comprising: 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-3, one or more compounds represented by formula IV-4, one or more compounds represented by formula IV-8, one or more compounds represented by formula VII 1, and at least one polymerizable compound, ##STR00034## wherein in formula III, R.sub.1 represents an alkoxy group having a carbon atom number of 2; R2 represent an alkoxy group having a carbon atom number of 2-4; R31 represents an alkyl group having a carbon atom number of 3; R41 represents an alkoxy group having a carbon atom number of 2; R.sub.101 represents an alkyl group having a carbon atom number of 2-4, where a total of the components other than the polymerizable compound is 100% by mass, a total mass content of the compound represented by formula I is 1%-47%; a total mass content of the compound represented by formula II is 1%-25%; a total mass content of the compound represented by formula III is 1%-35%; a total mass content of the compound represented by formula IV-3 is 3%; a total mass content of the compound represented by formula IV-4 is 9%; a total mass content of the compound represented by formula IV-8 is 13%; a total mass content of the compound represented by formula VII-1 is 3%-8%; and the polymerizable compound is added in an amount of 0.03%-0.4% on the basis of the total mass % of the liquid crystal.

2. The liquid crystal composition according to claim 1, wherein said liquid crystal composition further comprises one or more compounds represented by formula V: ##STR00035## wherein in formula V, R.sub.5 and R.sub.6 each independently represent an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10 or a fluorine-substituted alkenyl group having a carbon atom number of 2-10; and ##STR00036## each independently represent 1,4-cyclohexylene, 1,4-cyclohexenylene or 1,4-phenylene; furthermore, where ##STR00037## simultaneously represent 1,4-cyclohexylene, and one of R.sub.5 and R.sub.6 represents propyl, the other one of the R.sub.5 and R.sub.6 is not vinyl.

3. The liquid crystal composition according to claim 2, wherein said one or more compounds represented by formula V are selected from the group consisting of compounds represented by formulas V-1 to V-3: ##STR00038## wherein R.sub.5 and R.sub.6 each independently represent an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10 or a fluorine-substituted alkenyl group having a carbon atom number of 2-10; and in formula V-1, where one of R.sub.5 and R.sub.6 represents propyl, the other one of the R.sub.5 and R.sub.6 is not vinyl.

4. The liquid crystal composition according to claim 1, wherein said liquid crystal composition further comprises one or more selected from the group consisting of compounds represented by formula VI-1 to VI-3: ##STR00039## wherein R.sub.71 represents an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, or vinyl; and R.sub.72, R.sub.73 and R.sub.8 each independently represent an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10 or a fluorine-substituted alkenyl group having a carbon atom number of 2-10.

5. A liquid crystal display element, comprising the liquid crystal composition of claim 1, wherein said liquid crystal display element is an active matrix addressing display element, or a passive matrix addressing display element.

6. A liquid crystal display, comprising the liquid crystal composition of claim 1, wherein said liquid crystal display is an active matrix addressing display, or a passive matrix addressing 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, and at least one polymerizable compound.

(3) ##STR00003##

(4) wherein

(5) R.sub.1 and R.sub.2 each independently represent an alkoxy group having a carbon atom number of 1-10.

(6) As the alkoxy group having a carbon atom number of 1-10, examples include methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, pentyloxy, hexyloxy, heptyloxy, octyloxy, nonyloxy, decyloxy etc.

(7) In the liquid crystal composition of the present disclosure, the above-mentioned polymerizable compound is preferably selected from formulas RM-1 to RM-8

(8) ##STR00004##

(9) The liquid crystal composition of the present disclosure preferably further comprises one or more compounds represented by formula IV:

(10) ##STR00005##

(11) wherein R.sub.3 and R.sub.4 represent an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10, a fluorine-substituted alkenyl group having a carbon atom number of 2-10, an alkenoxy group having a carbon atom number of 3-8 or an fluorine-substituted alkenoxy group having a carbon atom number of 3-8, and any one or more unconnected CH.sub.2 in the groups represented by R.sub.3 and R.sub.4 are optionally substituted with cyclopentyl, cyclobutyl or cyclopropyl;

(12) Z.sub.1 and Z.sub.2 each independently represent a single bond, —CH.sub.2CH.sub.2— or —CH.sub.2O—;

(13) ##STR00006##
each independently represent 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene or a fluorinated 1,4-phenylene; and

(14) m and n each independently represent 0, 1 or 2, with m+n≤2;

(15) furthermore, where m+n=1, Z.sub.1 and Z.sub.2 are single bonds, and

(16) ##STR00007##
represent 1,4-phenylene, R.sub.3 and R.sub.4 do not simultaneously represent an alkoxy group having a carbon atom number of 1-10.

(17) In the liquid crystal composition of the present disclosure, preferably, the compound represented by formula IV mentioned above is selected from the group consisting of compounds represented by formula IV-1 to IV-14 below:

(18) ##STR00008## ##STR00009##

(19) wherein

(20) R.sub.31 represents an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10, a fluorine-substituted alkenyl group having a carbon atom number of 2-10, an alkenoxy group having a carbon atom number of 3-8 or an fluorine-substituted alkenoxy group having a carbon atom number of 3-8; R.sub.41 represents an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10, a fluorine-substituted alkenyl group having a carbon atom number of 2-10 or an alkenoxy group having a carbon atom number of 3-8; and any one or more unconnected CH.sub.2 in the groups represented by R.sub.31 and R.sub.41 are optionally substituted with cyclopentyl, cyclobutyl or cyclopropyl.

(21) In the liquid crystal composition of the present disclosure, preferably, where the total of the components other than the polymerizable compound is 100% by mass, the total mass content of the compound represented by formula I above is 1%-47%; the total mass content of the compound represented by formula II above is 1%-25%; the total mass content of the compound represented by formula III above is 1%-35%; and the polymerizable compound above is added in an amount of 0.01%-1%, preferably 0.03%-0.4% on the basis of the total mass % of the liquid crystal.

(22) The liquid crystal composition of the present disclosure preferably further comprises one or more compounds represented by formula V:

(23) ##STR00010##

(24) wherein

(25) R.sub.5 and R.sub.6 represent an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10 or a fluorine-substituted alkenyl group having a carbon atom number of 2-10; and

(26) ##STR00011##
each independently represent 1,4-cyclohexylene, 1,4-cyclohexenylene or 1,4-phenylene; furthermore, where

(27) ##STR00012##
simultaneously represent 1,4-cyclohexylene, and one of R.sub.5 and R.sub.6 represents propyl, the other one of the R.sub.5 and R.sub.6 does not represent vinyl.

(28) In the liquid crystal composition of the present disclosure, preferably, the compound represented by formula V mentioned above is selected from the group consisting of compounds represented by formula V-1 to V-3 below:

(29) ##STR00013##

(30) wherein R.sub.5 and R.sub.6 represent an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10 or a fluorine-substituted alkenyl group having a carbon atom number of 2-10; and in formula V-1, where one of R.sub.5 and R.sub.6 represents propyl, the other one of the R.sub.5 and R.sub.6 does not represent vinyl.

(31) The liquid crystal composition of the present disclosure preferably further comprises one or more selected from the group consisting of compounds represented by formula VI-1 to VI-3 below:

(32) ##STR00014##

(33) wherein

(34) R.sub.71 represents an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, or vinyl; and R.sub.72, R.sub.73 and R.sub.8 represent an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorine-substituted alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10 or a fluorine-substituted alkenyl group having a carbon atom number of 2-10.

(35) The liquid crystal composition of the present disclosure preferably further comprises one or more compounds represented by formula VII:

(36) ##STR00015##

(37) wherein

(38) R.sub.9 represents an alkyl group having a carbon atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10 or a fluorine-substituted alkoxy group having a carbon atom number of 1-10, and any one or more unconnected CH.sub.2 in these groups are optionally substituted with cyclopentyl, cyclobutyl or cyclopropyl;

(39) R.sub.10 represents an alkyl group having an atom number of 1-10, a fluorine-substituted alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10 or a fluorine-substituted alkoxy group having a carbon atom number of 1-10; and

(40) X represents O or S.

(41) In the liquid crystal composition of the present disclosure, preferably, the compound represented by formula VII mentioned above is selected from the group consisting of compounds represented by formula VII-1 to VII-12 below:

(42) ##STR00016## ##STR00017##

(43) wherein R.sub.91 and R.sub.101 represent an alkyl group having a carbon atom number of 1-10.

(44) [Liquid Crystal Display Element]

(45) The liquid crystal display element of the present disclosure comprises the liquid crystal composition of the present disclosure, which liquid crystal display element is an active matrix display element or a passive matrix display element.

(46) Optionally, said liquid crystal display element may be an active matrix liquid crystal display element.

(47) Optionally, said active matrix display element may be, for example, a PSVA-TFT liquid crystal display element.

(48) The liquid crystal display element comprising the liquid crystal composition of the present disclosure has a faster response speed and a smaller cell thickness.

(49) [Liquid Crystal Display]

(50) The liquid crystal display of the present disclosure comprises the liquid crystal composition of the present disclosure, which liquid crystal display is an active matrix display or a passive matrix display.

(51) Optionally, said liquid crystal display may be an active matrix liquid crystal display.

(52) Optionally, said active matrix display may be, for example, a PSVA-TFT liquid crystal display.

(53) The liquid crystal display comprising the liquid crystal composition of the present disclosure has a faster response speed and a smaller cell thickness.

EXAMPLE

(54) In order to more clearly illustrate the present disclosure, the present disclosure is further described below in conjunction with preferred examples. A person skilled in the art should understand that the content described in detail below is illustrative rather than limiting, and should not limit the scope of protection of the present disclosure.

(55) In this description, unless otherwise specified, percentages are mass percentages, temperatures are in degree Celsius (° C.), and the specific meanings of the other symbols and the test conditions are as follows:

(56) Cp represents the clearing point (° C.) of the liquid crystal measured by a DSC quantitative method;

(57) Δn represents optical anisotropy, n.sub.o is the refractive index of an ordinary light, n.sub.e is the refractive index of an extraordinary light, with the test conditions being: 25±2° C., 589 nm and using an abbe refractometer for testing;

(58) Δε represents the dielectric anisotropy, Δε=ε.sub.//−ε.sub.⊥, wherein ε.sub.// is a dielectric constant parallel to a molecular axis, and ε.sub.⊥ is a dielectric constant perpendicular to the molecular axis, the test condition is 25±0.5° C., a 20 micron parallel cell is used, and INSTEC: ALCT-IR1 is used for the test;

(59) γ1 represents a rotary viscosity (mPa.Math.s), with the test conditions being 25±0.5° C., a 20 micron parallel cell, and INSTEC: ALCT-IR1 for testing; and

(60) K11 is twist elastic constant, and K33 is splay elastic constant, with the test conditions being: 25° C., INSTEC:ALCT-IR1, and 18 μm vertical cell;

(61) A method for preparing the liquid crystal composition involves: weighing various liquid crystal monomers at a certain ratio and then placing them in a stainless steel beaker; placing the stainless steel beaker containing these liquid crystal monomers on a magnetic stirring instrument for heating and melting; and after the liquid crystal monomers in the stainless steel beaker are mostly melted, adding a magnetic rotor to the stainless steel beaker; uniformly stirring the mixture; and cooling the mixture to room temperature to obtain the liquid crystal composition.

(62) In the examples of the present disclosure, liquid crystal monomer structures are represented by codes, wherein the codes of cyclic structures, end groups and linking groups of liquid crystals are represented as follows in tables 1 and 2.

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

(64) TABLE-US-00002 TABLE 2 Corresponding code for end group and linking group End group and linking group Corresponding code C.sub.nH.sub.2n + .sub.1— n— C.sub.nH.sub.2n + .sub.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 + .sub.1 Vn— Cp— Cpr— Cpr1—

Examples

(65) ##STR00027##
the code of which is CC-Cp-V1;

(66) ##STR00028##
the code of which is CPY-2-O2;

(67) ##STR00029##
the code of which is CCY-3-O2;

(68) ##STR00030##
the code of which is COY-3-O2;

(69) ##STR00031##
the code of which is CCOY-3-O2;

(70) ##STR00032##
the code of which is Sb-Cp1O-O4; and

(71) ##STR00033##
the code of which is Sc-Cp1O-O4.

Example 1

(72) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 3 below.

(73) TABLE-US-00003 TABLE 3 Formulation of the liquid crystal composition of Example 1 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 40 II CCP-V2-1 25 III PY-2O-O2 15 III PY-2O-O4 10 III PY-1O-O2 10 RM-1 1 Δε [1 KHz, 25° C.]: −2.4 Δn [589 nm, 25° C.]: 0.105 Cp: 75° C. γ.sub.1: 71 mPa .Math. s K33: 17.6

Comparative Example 1

(74) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 4 below.

(75) TABLE-US-00004 TABLE 4 Formulation of the liquid crystal composition of Comparative Example 1 and the corresponding properties thereof Liquid crystal Content (in Category monomer code parts by mass) CC-5-V 40 II CCP-V2-1 25 III PY-2O-O2 15 III PY-2O-O4 10 III PY-1O-O2 10 RM-1 1 Δε [1 KHz, 25° C.]: −2.5 Δn [589 nm, 25° C.]: 0.107 Cp: 78° C. γ.sub.1: 95 mPa .Math. s K33: 18.2

(76) CC-3-V in Example 1 is replaced by CC-5-V to form Comparative Example 1. Compared with Comparative Example 1, Example 1 has no crystal precipitation at normal temperature, and differ to a smaller extent in the properties of dielectricity, refractive index and k value, but has a smaller rotary viscosity γ1 and a smaller γ1/K33, thus resulting in a faster response. It can be seen therefrom that the liquid crystal composition of the present disclosure has a good low-temperature mutual solubility and a fast response speed.

Comparative Example 2

(77) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 5 below.

(78) TABLE-US-00005 TABLE 5 Formulation of the liquid crystal composition of Comparative Example 2 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 40 CCP-3-1 25 III PY-2O-O2 15 III PY-2O-O4 10 III PY-1O-O2 10 RM-1 1 Δε [1 KHz, 25° C.]: −2.3 Δn [589 nm, 25° C.]: 0.104 Cp: 76° C. γ.sub.1: 73 mPa .Math. s K33: 17.2

(79) CCP-V2-1 in Example 1 is replaced by CCP-3-O1 to form Comparative Example 2. Compared with Comparative Example 2, Example 1 has no crystal precipitation at normal temperature, and differ to a smaller extent in the properties of dielectricity, refractive index and k value, but has a smaller rotary viscosity γ1 is and a smaller γ1/K33, thus resulting in a faster response. It can be seen therefrom that the liquid crystal composition of the present disclosure has a good low-temperature mutual solubility and a fast response speed.

Comparative Example 3

(80) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 6 below.

(81) TABLE-US-00006 TABLE 6 Formulation of the liquid crystal composition of Comparative Example 3 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 40 II CCP-V2-1 25 PY-3-O2 15 PY-2-O4 10 PY-1-O2 10 RM-1 1 Δε [1 KHz, 25° C.]: −2.1 Δn [589 nm, 25° C.]: 0.098 Cp: 64° C. γ.sub.1: 54 mPa .Math. s K33: 13.5

(82) PY-2O-O2, PY-2O-O4 and PY-1O-O2 in Example 1 are replaced by PY-3-O2, PY-2-O4 and PY-1-O2 to form Comparative Example 3, and by comparing Example 1 with Comparative Example 3, Example 1 has a large dielectricity, a high clearing point, and a large refractive index. It can be seen therefrom that the liquid crystal composition of the present disclosure can be used for the development of a liquid crystal composition having a small cell thickness and a fast response speed.

Example 2

(83) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 7 below.

(84) TABLE-US-00007 TABLE 7 Formulation of the liquid crystal composition of Example 2 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 45 II CCP-V2-1 7 III PY-2O-O2 3 III PY-2O-O4 7 IV CY-3-O2 15 IV PY-3-O2 3 IV CCY-2-O2 5 IV CCY-3-O2 11 IV CPY-3-O2 4 RM-1 0.01 Δε [1 KHz, 25° C.]: −3.0 Δn [589 nm, 25° C.]: 0.084 Cp: 65° C. γ.sub.1: 63 mPa .Math. s K33: 14.3

Example 3

(85) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 8 below.

(86) TABLE-US-00008 TABLE 8 Formulation of the liquid crystal composition of Example 3 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 35 II CCP-V2-1 12 III PY-2O-O2 3 IV CY-3-O2 8 IV CCY-2-O2 7 IV CCY-3-O2 5 IV COY-3-O2 5 IV PY-3-O2 14 IV CCOY-3-O2 11 RM-3 0.03 Δε [1 KHz, 25° C.]: −4.2 Δn [589 nm, 25° C.]: 0.078 Cp: 55° C. γ.sub.1: 70 mPa .Math. s K33: 12.3

Example 4

(87) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 9 below.

(88) TABLE-US-00009 TABLE 9 Formulation of the liquid crystal composition of Example 4 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 19.5 II CCP-V2-1 9 III PY-2O-O2 5 III PY-2O-O4 10 IV CY-3-O2 7.7 IV CCY-2-O2 7 IV COY-3-O2 5 IV CCOY-3-O2 13 V CC-3-V1 5 V CC-2-3 11 V CC-4-3 3 V PP-5-1 3 V CP-3-O2 1.8 RM-3 0.36 Δε [1 KHz, 25° C.]: −3.6 Δn [589 nm, 25° C.]: 0.088 Cp: 68° C. γ.sub.1: 87 mPa .Math. s K33: 15.1

Example 5

(89) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 10 below.

(90) TABLE-US-00010 TABLE 10 Formulation of the liquid crystal composition of Example 5 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 5.5 II CCP-V2-1 9 III PY-2O-O2 2 III PY-2O-O4 7 IV PY-3-O2 11 IV CCOY-3-O2 13 IV CY-3-O2 16.5 V CC-2-3 19.5 V CC-4-3 7 VI-1 CCP-3-O1 7 VI-1 CCP-V-1 2.5 RM-3 0.36 Δε [1 KHz, 25° C.]: −3.3 Δn [589 nm, 25° C.]: 0.087 Cp: 67° C. γ.sub.1: 85 mPa .Math. s K33: 13.0

Example 6

(91) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 11 below.

(92) TABLE-US-00011 TABLE 11 Formulation of the liquid crystal composition of Example 6 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 1 II CCP-V2-1 11 III PY-2O-O2 7 IV COY-3-O2 13 IV CPY-3-O2 11 IV PY-3-O2 13 V CP-3-O2 11 V CC-2-3 7 V CC-5-3 7 VI-1 CCP-V-1 7 VI-2 CPP-3-2 5 VII Sb-CP1O-O4 2 VII Sc-CP1O-O4 5 RM 0.07 Δε [1 KHz, 25° C.]: −3.7 Δn [589 nm, 25° C.]: 0.114 Cp: 70° C. γ.sub.1: 88 mPa .Math. s K33: 13.1

Example 7

(93) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 12 below.

(94) TABLE-US-00012 TABLE 12 Formulation of the liquid crystal composition of Example 7 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 13.5 II CCP-V2-1 3 III PY-2O-O2 3 III PY-2O-O4 9 IV PY-3-O2 9 IV COY-3-O2 11 IV CCY-3-O2 15 IV CCOY-3-O2 12 V CC-2-3 5 V CC-4-3 9 V CP-5-O2 3.5 V PP-5-1 1 VI-2 CPP-3-2V1 6 RM-5 0.23 Δε [1 KHz, 25° C.]: −4.0 Δn [589 nm, 25° C.]: 0.093 Cp: 52° C. γ.sub.1: 72 mPa .Math. s K33: 10.9

Example 8

(95) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 13 below.

(96) TABLE-US-00013 TABLE 13 Formulation of the liquid crystal composition of Example 8 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 29.5 II CCP-V2-1 5 III PY-2O-O2 1 IV PY-3-O2 11 IV CCY-3-O2 10.5 IV CCOY-3-O2 12 V CC-2-3 5 V CP-3-O2 5 V CC-3-V1 8 VI-1 CCP-V-1 7 VI-2 CPP-3-2 3 VII Sb-Cp1O-O4 3 RM-4 0.38 Δε [1 KHz, 25° C.]: −2.8 Δn [589 nm, 25° C.]: 0.089 Cp: 82° C. γ.sub.1: 83 mPa .Math. s K33: 17.0

Comparative Example 4

(97) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 14 below.

(98) TABLE-US-00014 TABLE 14 Formulation of the liquid crystal composition of Comparative Example 4 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 29.5 CCP-3-1 5 III PY-2O-O2 1 IV PY-3-O2 11 IV CCY-3-O2 10.5 IV CCOY-3-O2 12 V CC-2-3 5 V CP-3-O2 5 V CC-3-V1 8 VI-1 CCP-V-1 7 VI-2 CPP-3-2 3 VII Sb-Cp1O-O4 3 RM-4 0.38 Δε [1 KHz, 25° C.]: −2.8 Δn [589 nm, 25° C.]: 0.088 Cp: 81° C. γ.sub.1: 88 mPa .Math. s K33: 17.1

(99) CCP-V2-1 in Example 8 is replaced by CCP-3-1 to form Comparative Example 4. Compared with Comparative Example 4, Example 8 differ to a smaller extent in the properties of dielectricity, refractive index, cleaning point and K33; however, Example 8 has a smaller γ1, a smaller γ1/K33, and a faster response. It can be seen therefrom that the liquid crystal composition of the present disclosure has the advantage of a fast response speed, and when applied to the manufacture procedure for an ODF liquid crystal display device, there is no defective displaying in the liquid crystal display device.

Example 9

(100) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 15 below.

(101) TABLE-US-00015 TABLE 15 Formulation of the liquid crystal composition of Example 9 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 13.5 II CCP-V2-1 10 III PY-2O-O2 5 IV PY-3-O2 3 IV CCY-3-O2 11 IV CCOY-3-O2 7 IV COY-3-O2 10 V CC-2-3 12 V CC-5-3 7 V PP-5-O2 9 VI-1 CCP-3-O1 7 VI-2 CPP-1V-2 5.5 RM-5 0.25 Δε [1 KHz, 25° C.]: −2.7 Δn [589 nm, 25° C.]: 0.100 Cp: 91° C. γ.sub.1: 91 mPa .Math. s K33: 18

Example 10

(102) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 16 below.

(103) TABLE-US-00016 TABLE 16 Formulation of the liquid crystal composition of Example 10 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 19 II CCP-V2-1 11 III PY-2O-O2 5 IV COY-3-O2 13 IV PY-3-O2 15 IV LY-Cp-O2 3 V CC-4-3 2.5 V CC-5-3 5 V CP-3-O2 1 VI-1 CCP-V-1 5 VI-2 CPP-3-2 2.5 VI-1 CCP-3-O1 2 VI-2 CPP-1V-2 1 VI-2 CPP-3-2V1 7 VII Sc-Cp1O-O4 8 RM-1 0.15 Δε [1 KHz, 25° C.]: −3.0 Δn [589 nm, 25° C.]: 0.107 Cp: 70° C. γ.sub.1: 66 mPa .Math. s K33: 12.7

Example 11

(104) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 17 below.

(105) TABLE-US-00017 TABLE 17 Formulation of the liquid crystal composition of Example 11 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 35 II CCP-V2-1 12 III PY-2O-O2 11 III PY-2O-O4 18 III PY-1O-O4 1 V CC-2-3 5 V CC-4-3 7 V CP-5-O2 9 V CP-3-O2 2 RM-4 0.33 Δε [1 KHz, 25° C.]: −2.1 Δn [589 nm, 25° C.]: 0.091 Cp: 60° C. γ.sub.1: 61 mPa .Math. s K33: 13.2

Example 12

(106) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 18 below.

(107) TABLE-US-00018 TABLE 18 Formulation of the liquid crystal composition of Example 12 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 17 II CCP-V2-1 5 III PY-2O-O2 8 IV PY-3-O2 13 IV COY-3-O2 11 IV CCOY-2-O2 14 IV CCOY-3-O2 15 VI-2 CPP-3-2 3 VI-1 CCP-3-1 2 VI-1 CCP-V-1 7 VI-2 CPP-1V-2 2 VI-2 CPP-3-2V1 3 RM-3 0.29 Δε [1 KHz, 25° C.]: −4.5 Δn [589 nm, 25° C.]: 0.109 Cp: 87° C. γ.sub.1: 141 mPa .Math. s K33: 16.8

Example 13

(108) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 19 below.

(109) TABLE-US-00019 TABLE 19 Formulation of the liquid crystal composition of Example 13 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 33 II CCP-V2-1 9 III PY-2O-O2 5 III PY-2O-O4 9 IV CY-3-O2 5 IV CPY-3-O2 11 IV CCOY-3-O2 7 VI-1 CCP-3-1 3 VI-1 CCP-V-1 9 VI-2 CPP-1V-2 2 VII Sb-4O-O4 2 VII Sc-2O-O4 5 RM-1 0.09 Δε [1 KHz, 25° C.]: −3.2 Δn [589 nm, 25° C.]: 0.110 Cp: 90° C. γ.sub.1: 96 mPa .Math. s K33: 18.5

Comparative Example 5

(110) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 20 below.

(111) TABLE-US-00020 TABLE 20 Formulation of the liquid crystal composition of Comparative Example 5 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 33 CCP-3-O1 9 III PY-2O-O2 5 III PY-2O-O4 9 IV CY-3-O2 5 IV CPY-3-O2 11 IV CCOY-3-O2 7 VI-1 CCP-3-1 3 VI-1 CCP-V-1 9 VI-2 CPP-1V-2 2 VII Sb-4O-O4 2 VII Sc-2O-O4 5 RM-1 0.09 Δε [1 KHz, 25° C.]: −3.1 Δn [589 nm, 25° C.]: 0.111 Cp: 90° C. γ.sub.1: 106 mPa .Math. s K33: 18.5

(112) CCP-V2-1 in Example 13 is replaced by CCP-3-O1 to form Comparative Example 5. Compared with Comparative Example 5, Example 13 differ to a smaller extent in the properties of dielectricity, refractive index, cleaning point and K33; however, Example 13 has a smaller γ1, a smaller γ1/K33, and a faster response. It can be seen therefrom that the liquid crystal composition of the present disclosure has the advantage of a fast response.

Example 14

(113) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 21 below.

(114) TABLE-US-00021 TABLE 21 Formulation of the liquid crystal composition of Example 14 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 19 II CPP-V2-1 5 III PY-2O-O2 5 III PY-2O-O4 10 IV PY-3-O2 7 IV COY-3-O2 7 IV CCOY-3-O2 12 V CC-2-3 20 V CC-5-3 3 V CP-5-O2 4 VII Sb-Cp1O-O4 3 VII Sc-Cp1O-O2 5 RM-2 0.33 Δε [1 KHz, 25° C.]: −4.1 Δn [589 nm, 25° C.]: 0.090 Cp: 53° C. γ.sub.1: 74 mPa .Math. s K33: 11.5

Example 15

(115) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 22 below.

(116) TABLE-US-00022 TABLE 22 Formulation of the liquid crystal composition of Example 15 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) I CC-3-V 13 II CCP-V2-1 5 III PY-2O-O2 3 III PY-2O-O4 5 IV PY-3-O2 3 IV CCY-3-O2 9 IV CCOY-3-O2 13 V CC-2-3 19 V CC-4-3 5 V CC-3-V1 3 V CP-5-O2 3 VI-1 CCP-V-1 7 VI-2 CPP-1V-2 3 VI-1 CPP-3-2 4 VII Sb-Cp1O-O4 3 VII Sc-Cp1O-O2 2 RM-4 0.31 Δε [1 KHz, 25° C.]: −3.0 Δn [589 nm, 25° C.]: 0.095 Cp: 88° C. γ.sub.1: 107 mPa .Math. s K33: 16.9

Comparative Example 6

(117) The formulation of the liquid crystal composition and the corresponding properties thereof are as shown in table 23 below.

(118) TABLE-US-00023 TABLE 23 Formulation of the liquid crystal composition of Comparative Example 6 and the corresponding properties thereof Liquid crystal Content (in parts Category monomer code by mass) CC-5-V 13 II CCP-V2-1 5 III PY-2O-O2 3 III PY-2O-O4 5 IV PY-3-O2 3 IV CCY-3-O2 9 IV CCOY-3-O2 13 V CC-2-3 19 V CC-4-3 5 V CC-3-V1 3 V CP-5-O2 3 VI-1 CCP-V-1 7 VI-2 CPP-1V-2 3 VI-1 CPP-3-2 4 VII Sb-Cp1O-O4 3 VII Sc-Cp1O-O2 2 RM-4 0.31 Δε [1 KHz, 25° C.]: −3.0 Δn [589 nm, 25° C.]: 0.096 Cp: 90° C. γ.sub.1: 118 mPa .Math. s K33: 17.1

(119) CC-3-V in Example 15 is replaced by CC-5-V to form Comparative Example 6. Compared with Comparative Example 6, Example 15 differ to a smaller extent in the properties of dielectricity, refractive index, cleaning point and K33; however, Example 15 has a smaller γ1, a smaller γ1/K33, and a faster response. It can be seen therefrom that the liquid crystal composition of the present disclosure has the advantage of a fast response.

(120) Obviously, the above-mentioned examples of the present disclosure are merely examples for clearly illustrating the present disclosure, rather than limiting the embodiments of the present disclosure; for a person of ordinary skill in the art, on the basis of the above description, other variations or changes in different forms may also be made, it is impossible to exhaustively give all of the embodiments thereof herein, and any obvious variation or change derived from the technical solution of the present invention is still within the scope of protection of the present invention.