LIQUID CRYSTAL COMPOSITION HAVING NEGATIVE DIELECTRIC ANISOTROPY AND DISPLAY DEVICE THEREOF

Abstract

The present invention discloses a liquid crystal composition comprising: 15-35% by weight of a compound of general formula I; 3-20% by weight of a compound of general formula II; 5-30% by weight of a compound of general formula III; 1-20% by weight of a compound of general formula IV; 10-35% by weight of a compound of general foiiiiula V-1 and/or a compound of general formula V-2; and 1-25% by weight of a compound of general formula VI. The liquid crystal composition provided by the present invention has the characteristics of an appropriate optical anisotropy, an appropriate dielectric anisotropy, a higher clearing point, a better voltage holding ratio, and a good UV-resistant stability, etc., and can be applied to a liquid crystal display.

##STR00001##

Claims

1. A liquid crystal composition having a negative dielectric anisotropy, comprising: 15-35% by weight of a compound of general foimula I, ##STR00030## 3-20% by weight of a compound of general formula II, ##STR00031## 5-30% by weight of a compound of general formula III, ##STR00032## 1-20% by weight of a compound of general formula IV, ##STR00033## 10-35% by weight of a compound of general formula V-1 and/or a compound of general formula V-2, ##STR00034## and 1-25% by weight of a compound of general formula VI, ##STR00035## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.9, R.sub.10, R.sub.11 and R.sub.13 are the same or different and each independently represents an alkyl group having a carbon atom number of 1 to 5; R.sub.6, R.sub.12 and R.sub.14 are the same or different, and each independently represents an alkyl group having a carbon atom number of 1 to 5 or an alkoxy group having a carbon atom number of 1 to 5; R.sub.7 and R.sub.8 are the same or different, and each independently represents H or an alkyl group having a carbon atom number of 1 to 10, wherein one or more non-adjacent CH.sub.2 groups may be replaced by O, CO, COO, OCOO or OCO, the oxygen atoms are not directly connected, and one or more H atoms can be replaced by fluorine; L.sub.1 represents H or F; Z.sub.1 and Z.sub.2 are the same or different, and each independently represents CH.sub.2O, OCH.sub.2, O, CH.sub.2CH.sub.2 or a single bond, and at least one of Z.sub.1 and Z.sub.2 is CH.sub.2O, OCH.sub.2 or O; A and B are the same or different, and each independently represents 1,4-cyclohexylene or 1,3-cyclopentylene, wherein one or more non-adjacent CH.sub.2 groups may be replaced by O; and m and n are the same or different, and each independently represents 0, 1 or 2, with n+m2.

2. The liquid crystal composition having a negative dielectric anisotropy according to claim 1, wherein the compound of general formula I is one or more compounds selected from the group consisting of the following compounds: ##STR00036##

3. The liquid crystal composition having a negative dielectric anisotropy according to claim 1, wherein the compound of general formula II is one or more compounds selected from the group consisting of the following compounds: ##STR00037##

4. The liquid crystal composition having a negative dielectric anisotropy according to claim 1, wherein the compound of general formula III is one or more compounds selected from the group consisting of the following compounds: ##STR00038##

5. The liquid crystal composition having a negative dielectric anisotropy according to claim 1, wherein the compound of general formula IV is one or more compounds selected from the group consisting of the following compounds: ##STR00039## wherein R.sub.7 and R.sub.8 are the same or different, and each independently represents an alkyl group having a carbon atom number of 1 to 10, wherein one or more H atoms can be replaced by fluorine; L.sub.1 represents H or F; Z.sub.3, Z.sub.4, Z.sub.5, Z.sub.6 and Z.sub.7 are the same or different, and each independently represents CH.sub.2O, OCH.sub.2, O, CH.sub.2CH.sub.2 or a single bond; p, q, r, s and t are the same or different, and each independently represents 0 or 1, with p+q1.

6. The liquid crystal composition having a negative dielectric anisotropy according to claim 1, wherein the compound of general formula VI is one or more compounds selected from the group consisting of the following compounds: ##STR00040## wherein R.sub.15 and R.sub.16 are the same or different, and each independently represents an alkyl group having a carbon atom number of 1 to 5.

7. The liquid crystal composition having a negative dielectric anisotropy according to claim 5, wherein the compound of general foiiiiula IV-1 is one or more compounds selected from the group consisting of the following compounds: ##STR00041## the compound of general formula IV-2 is one or more compounds selected from the group consisting of the following compounds: ##STR00042## the compound of general formula IV-3 is one or more compounds selected from the group consisting of the following compounds: ##STR00043## the compound of general formula IV-4 is one or more compounds selected from the group consisting of the following compounds: ##STR00044## and the compound of general formula IV-5 is one or more compounds selected from the group consisting of the following compounds: ##STR00045## wherein R.sub.7 and R.sub.8 are the same or different, and each independently represents an alkyl group having a carbon atom number of 1 to 5.

8. The liquid crystal composition having a negative dielectric anisotropy according to claim 1, wherein the compound of general formula III accounts for 10-30% of the total weight of said liquid crystal composition; the compound of general formula IV accounts for 3-20% of the total weight of said liquid crystal composition; the compound of general formula V-1 and/or general formula V-2 accounts for 12-30% of the total weight of said liquid crystal composition; and the compound of general formula VI-1 accounts for 3-18% of the total weight of said liquid crystal composition.

9. The liquid crystal composition having a negative dielectric anisotropy according to claim 8, wherein the compound of general formula VI-1 accounts for 5-15% of the total weight of said liquid crystal composition.

10. The liquid crystal composition having a negative dielectric anisotropy according to claim 9, wherein said liquid crystal composition comprises: a compound accounting for 20% of the total weight of said liquid crystal composition: ##STR00046## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00047## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00048## a compound accounting for 8% of the total weight of said liquid crystal composition: ##STR00049## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00050## a compound accounting for 2% of the total weight of said liquid crystal composition: ##STR00051## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00052## a compound accounting for 10% of the total weight of said liquid crystal composition: ##STR00053## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00054## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00055## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00056## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00057## and a compound accounting for 18% of the total weight of said liquid crystal composition: ##STR00058## or said liquid crystal composition comprises: a compound accounting for 20% of the total weight of said liquid crystal composition: ##STR00059## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00060## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00061## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00062## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00063## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00064## a compound accounting for 2% of the total weight of said liquid crystal composition: ##STR00065## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00066## a compound accounting for 10% of the total weight of said liquid crystal composition: ##STR00067## a compound accounting for 8% of the total weight of said liquid crystal composition: ##STR00068## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00069## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00070## a compound accounting for 11% of the total weight of said liquid crystal composition: ##STR00071## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00072## and a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00073## or said liquid crystal composition comprises: a compound accounting for 23% of the total weight of said liquid crystal composition: ##STR00074## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00075## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00076## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00077## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00078## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00079## a compound accounting for 10% of the total weight of said liquid crystal composition: ##STR00080## a compound accounting for 11% of the total weight of said liquid crystal composition: ##STR00081## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00082## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00083## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00084## a compound accounting for 10% of the total weight of said liquid crystal composition: ##STR00085## a compound accounting for 2% of the total weight of said liquid crystal composition: ##STR00086## and a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00087## or said liquid crystal composition comprises: a compound accounting for 12% of the total weight of said liquid crystal composition: ##STR00088## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00089## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00090## a compound accounting for 8% of the total weight of said liquid crystal composition: ##STR00091## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00092## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00093## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00094## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00095## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00096## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00097## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00098## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00099## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00100## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00101## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00102## a compound accounting for 9% of the total weight of said liquid crystal composition: ##STR00103## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00104## and a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00105## or said liquid crystal composition comprises: a compound accounting for 12% of the total weight of said liquid crystal composition: ##STR00106## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00107## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00108## a compound accounting for 12% of the total weight of said liquid crystal composition: ##STR00109## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00110## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00111## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00112## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00113## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00114## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00115## a compound accounting for 6% of the total weight of said liquid crystal composition: ##STR00116## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00117## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00118## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00119## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00120## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00121## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00122## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00123## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00124## or said liquid crystal composition comprises: a compound accounting for 23% of the total weight of said liquid crystal composition: ##STR00125## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00126## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00127## a compound accounting for 4% of the total weight of said liquid crystal composition: ##STR00128## a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00129## a compound accounting for 7% of the total weight of said liquid crystal composition: ##STR00130## a compound accounting for 10% of the total weight of said liquid crystal composition: ##STR00131## a compound accounting for 11% of the total weight of said liquid crystal composition: ##STR00132## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00133## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00134## a compound accounting for 5% of the total weight of said liquid crystal composition: ##STR00135## a compound accounting for 11% of the total weight of said liquid crystal composition: ##STR00136## a compound accounting for 2% of the total weight of said liquid crystal composition: ##STR00137## and a compound accounting for 3% of the total weight of said liquid crystal composition: ##STR00138##

11. A mixture comprising the liquid crystal composition having a negative dielectric anisotropy of claim 1 and one or more polymerizable liquid crystal compounds complying with the following formula RM: ##STR00139## wherein P.sub.1 and P.sub.2 are the same or different, and each independently represents ##STR00140## L.sub.2 represents H or F.

12. A liquid crystal display, comprising the liquid crystal composition having a negative dielectric anisotropy of claim 1.

13. A liquid crystal display, comprising the mixture of claim 11.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0066] The present invention will be illustrated in conjunction with particular embodiments. It should be noted that the following embodiments are examples of the present invention, and are merely used for describing rather than limiting the present invention. Without departing from the subject matter or scope of the present invention, other combinations or various modifications can be made within the concept of the present invention.

[0067] For the ease of expression, in the following embodiments, group structures of the liquid crystal composition are represented by codes listed in table 1:

TABLE-US-00001 TABLE 1 Codes of group structures of the liquid crystal composition Unit structure of a group Code Group name [00023] C 1,4-cyclohexylene [00024] P 1,4-phenylene [00025] C(5) Cyclopentyl [00026] W 2,3-difluoro-1,4-phenylene O O Oxygen substituent CH.sub.2O 1O Methyleneoxy CH.sub.2CH.sub.2 2 Ethylidene CHCH V Alkenyl C.sub.nH.sub.2n-1 or C.sub.mH.sub.2m-1 n or m Alkyl

[0068] Taking a compound of the following structure formula for example:

##STR00027##

[0069] if expressed by the codes listed in table 1, the structure formula can be expressed as: C(5)PPOn, wherein n in the code represents the number of C atoms of an alkyl group on the right end, for example, n is 3, i.e. indicating that the alkyl group is C.sub.3H.sub.7; C(5) in the code represents cyclopentyl; P in the code represents 1,4-phenylene; and O in the code represents an oxygen substituent.

[0070] Abbreviated codes of test items in the following embodiments are as follows:

[0071] Cp( C.): clearing point (nematic-isotropic phase transition temperature)

[0072] n: optical anisotropy (589 nm, 20 C.)

[0073] : dielectric anisotropy (1 KHz, 25 C.)

[0074] VHR (initial): voltage holding ratio (%)

[0075] VHR (UV, 15 min): Voltage holding ratio after irradiation with a UV lamp for 15 min (%)

[0076] wherein the refractive index anisotropy is measured using an Abbe refractometer with a light source of sodium lamp (589 nm) at 20 C.; and the dielectric test cell is of TN90 type, and has a cell thickness of 7 m.

[0077] =, wherein is a dielectric constant parallel to a molecular axis, is a dielectric constant perpendicular to the molecular axis, and the test conditions are: 25 C., 1 KHz, and a dielectric test cell of TN90 type having a cell thickness of 7 m.

[0078] The VHR (initial) is measured using a TOY06254 type liquid crystal physical property evaluation system; and the test temperature is 60 C., the test voltage is 5 V, and the test time is 166.7 ms. The VHR (UV) is measured using the TOY06254 type liquid crystal physical property evaluation system after irradiation for 15 min with a UV lamp having an intensity of 5.8 mw/cm.sup.2 at 365 nm; and the test temperature is 60 C., the test voltage is 5 V, and the test time is 166.7 ms.

[0079] Various components adopted in the following embodiments can all be synthesized by well-known methods or obtained through commercial approaches. These synthesis techniques are conventional, and the obtained liquid crystal compounds comply with standards of electronic compounds after measurement.

[0080] Liquid crystal compositions are prepared according to the proportions of the various liquid crystal compositions specified in the following embodiments. The preparation of said liquid crystal compositions is carried out according to conventional methods in the art, such as heating, ultrasonic wave, suspension, etc., according to the specified proportions.

COMPARATIVE EXAMPLE 1

[0081] A liquid crystal composition M1 of comparative example 1 is formulated according to various compounds and weight percentages listed in table 2, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00002 TABLE 2 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Performance name type percentage parameter test result 5CCV 13 Cp 81.7 V2PP1 5 n 0.107 3CCV1 9 3.0 VCCP1 9 VHR (initial) 97.3% 3CPP2 4 VHR (UV, 84.1% 15 mm) 3CWO4 16 5CWO2 12 3CCWO2 VI-1 6 3CCWO3 VI-1 4 3CPWO2 III-8 8 3PWP2 4 3CCW1 VI 5 2CCW1 VI 5 Total 100

COMPARATIVE EXAMPLE 2

[0082] A liquid crystal composition M2 of comparative example 2 is formulated according to various compounds and weight percentages listed in table 3, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00003 TABLE 3 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Performance name type percentage parameter test result 3CC2 I-1 13 Cp 81.2 5PP1 I-4 5 n 0.108 4CC3 I-2 9 3.0 3CCP1 5 VHR (initial) 97.5% 3CPP2 8 VHR (UV, 94.0% 15 min) 3CWO4 15 5CWO2 10 3CCWO2 VI-1 6 3CCWO3 VI-1 7 3CPWO2 III-8 8 3CPPC3 4 3CCW1 VI 5 2CCW1 VI 5 Total 100

EXAMPLE 1

[0083] A liquid crystal composition N1 of example 1 is formulated according to various compounds and weight percentages listed in table 4, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00004 TABLE 4 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Performance name type percentage parameter test result 3CC2 I-1 20 Cp 81.2 4CC3 I-2 5 n 0.107 3PP2 II-2 6 3.1 5PP1 II-4 8 VHR (initial) 97.3% 3PPO2 IV-1-c 6 VHR (UV, 15 94.6% min) 3PPO4 IV-1-c 2 2CPWO2 III-7 5 3CPWO2 III-8 10 3CCWO2 VI-1 4 4CCWO2 VI-1 4 3C1OWO2 V-1-b 5 2CC1OWO2 V-2-a 7 3CC1OWO2 V-2-b 18 Total 100

EXAMPLE 2

[0084] A liquid crystal composition N2 of example 2 is formulated according to various compounds and weight percentages listed in table 5, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00005 TABLE 5 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Performance name type percentage parameter test result 3CC2 I-1 20 Cp 81.8 4CC3 I-2 6 n 0.11 3PP2 II-2 6 2.9 3PPO2 IV-1-c 6 VHR (initial) 97.5% 3PPO4 IV-1-c 4 VHR (UV, 94.3% 15 min) 3CPPO2 IV-1-c 3 3C1OPP2 IV-2-e 2 2CPWO2 III-7 5 3CPWO2 III-8 10 3CPWO4 III-9 8 3CCWO2 VI-1 4 4CCWO2 VI-1 4 3C1OWO2 V-1-b 11 2CC1OWO2 V-2-a 5 3CC1OWO2 V-2-b 6 Total 100

EXAMPLE 3

[0085] A liquid crystal composition N3 of example 3 is formulated according to various compounds and weight percentages listed in table 6, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00006 TABLE 6 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Performance name type percentage parameter test result 3CC2 I-1 23 Cp 82.3 4CC3 I-2 7 n 0.106 5CC2 I-3 3 3.1 3PP2 II-2 4 VHR (initial) 97.3% 3PPO2 IV-1-c 6 VHR (UV, 94.4% 15 min) 2CPWO2 III-7 7 3CPWO2 III-8 10 3CPWO4 III-9 11 3CCWO2 VI-1 4 4CCWO2 VI-1 5 3CCWO3 VI-1 5 3C1OWO2 V-1-b 10 2CC1OWO2 V-2-a 2 3CCIOWO2 V-2-b 3 Total 100

EXAMPLE 4

[0086] A liquid crystal composition N4 of example 4 is formulated according to various compounds and weight percentages listed in table 7, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00007 TABLE 7 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Perfonuance name type percentage parameter test result 3CC2 I-1 12 Cp 81.2 4CC3 I-2 5 n 0.113 3PP2 II-2 6 3.2 5PP1 II-4 8 VHR (initial) 97.6% 3PPO2 IV-1-c 6 VHR (UV, 94.5% 15 min) 3PPO4 IV-1-c 5 (C5)PPO2 IV-3-a 3 (C5)PPO4 IV-3-a 3 2CPWO2 III-7 3 3CPWO2 III-8 3 3CCWO2 VI-1 6 4CCWO2 VI-1 4 5CCWO2 VI-1 3 3C1OWO2 V-1-b 7 2CC1OWO2 V-2-a 7 3CC1OWO2 V-2-b 9 4CC1OWO2 V-2-c 5 5CC1OWO2 V-2-d 5 Total 100

EXAMPLE 5

[0087] A liquid crystal composition N5 of example 5 is formulated according to various compounds and weight percentages listed in table 8, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00008 TABLE 8 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Performance name type percentage parameter test result 3CC2 I-1 12 Cp 82.5 4CC3 I-2 5 n 0.111 3PP2 II-2 7 3.0 5PP1 II-4 12 VHR (initial) 97.6% 3PPO2 IV-1-c 3 VHR (UV, 94.4% 15 min) 3PPO4 IV-1-c 3 (C5)PPO2 IV-3-a 3 (C5)PPO4 IV-3-a 3 2CPWO2 III-7 3 3CPWO2 III-8 3 3CCWO2 VI-1 6 4CCWO2 VI-1 5 5CCWO2 VI-1 4 3CCWO3 VI-1 4 3C1OWO2 V-1-b 7 2CC1OWO2 V-2-a 5 3CC1OWO2 V-2-b 7 4CC1OWO2 V-2-c 4 5CC1OWO2 V-2-d 4 Total 100

EXAMPLE 6

[0088] A liquid crystal composition N6 of example 6 is formulated according to various compounds and weight percentages listed in table 9, and is filled between two substrates of a liquid crystal display for performance test, the test data being as shown in the following table:

TABLE-US-00009 TABLE 9 Formulation and testing performance of the liquid crystal composition Monomer Compound Weight Performance name type percentage parameter test result 3CC2 I-1 23 Cp 83.3 4CC3 I-2 7 n 0.101 5CC2 I-3 4 3.1 3PP2 II-2 4 VHR (initial) 97.3% 3PPO2 IV-1-c 3 VHR (UV, 94.8% 15 min) 2CPWO2 III-7 7 3CPWO2 III-8 10 3CPWO4 III-9 11 3CCWO2 VI-1 5 4CCWO2 VI-1 5 3CCWO3 VI-1 5 3C1OWO2 V-1-b 11 2CC1OWO2 V-2-a 2 3CC1OWO2 V-2-b 3 Total 100

[0089] It can be seen from the data of the above embodiments that the liquid crystal composition provided by the present invention has an appropriate optical anisotropy, an appropriate dielectric anisotropy, a broader nematic phase temperature range, and a higher clearing point, and can be applied to a liquid crystal display. In addition, compared with comparative examples 1 and 2, when the optical anisotropy values, the dielectric anisotropy values and the clearing points are close, the liquid crystal composition provided by the present invention has a better UV-resistant stability, and achieves obvious technical progress.

EXAMPLE 7

[0090] 0.3% of RM1 is added to the above-mentioned liquid crystal compositions M1, M2, N1, N2, N3, N4, N5 and N6, respectively:

##STR00028##

[0091] Mixtures M1RM1, M2RM1, N1RM1, N2RM1, N3RM1, N4RM1, N5RM1 and N6RM1 are obtained, the pretilt angle and VHR before and after UV illumination are measured, and the experimental results are shown in the following table:

TABLE-US-00010 TABLE 10 Pretilt angle before and after UV illumination Pretilt angle before Pretilt angle after Mixture UV illumination () UV illumination () M1RM1 89 88.1 M2RM1 89 87.8 N1RM1 89 84.8 N2RM1 89 83.1 N3RM1 89 84.9 N4RM1 89 82.7 N5RM1 89 83.4 N6RM1 89 85.3

TABLE-US-00011 TABLE 11 VHR before and after UV illumination VHR before UV VHR after UV Mixture illumination (%) illumination (%) M1RM1 96.9 86.6 M2RM1 97 97.1 N1RM1 97 97.8 N2RM1 96.9 98.3 N3RM1 96.8 98 N4RM1 97.3 98.8 N5RM1 97.2 98.3 N6RM1 96.8 97.7

EXAMPLE 8

[0092] 0.3% of RM2 is added to the above-mentioned liquid crystal compositions M1, M2, N1, N2, N3, N4, N5 and N6, respectively:

##STR00029##

[0093] Mixtures M1RM2, M2RM2, N1RM2, N2RM2, N3RM2, N4RM2, N5RM2 and N6RM2 are obtained, the pretilt angle and VHR before and after UV illumination are measured, and the experimental results are shown in the following table:

TABLE-US-00012 TABLE 12 Pretilt angle before and after UV illumination Pretilt angle before Pretilt angle after Mixture UV illumination () UV illumination () M1RM2 89 88.8 M2RM2 89 88.3 N1RM2 89 85.4 N2RM2 89 83.6 N3RM2 89 85.4 N4RM2 89 83.1 N5RM2 89 83.6 N6RM2 89 85.7

TABLE-US-00013 TABLE 13 VHR before and after UV illumination VHR before UV VHR after UV Mixture illumination (%) illumination (%) M1RM1 96.9 85.1 M2RM1 97 97.1 N1RM1 97 97.7 N2RM1 96.9 98 N3RM1 96.8 97.9 N4RM1 97.3 98.6 N5RM1 97.2 98.3 N6RM1 96.8 97.5

[0094] Likewise, the experimental results indicate that after 0.3% of RM3 and 0.3% of RM4 are added into N1, N2, N3, N4, N5 and N6, respectively, they likewise have a very good pretilt angle forming ability, and a better VHR value and pretilt angle forming ability after UV illumination.

[0095] It is indicated from the data of the above examples that the liquid crystal composition provided by the present invention as compared to the prior art has a better pretilt angle forming ability, enabling a polymer-stabilized vertical alignment display element to have a better optical effect, the liquid crystal composition of the present invention has a better VHR value after UV illumination, and the liquid crystal display device using the liquid crystal composition of the present invention has a better stability, achieving very good technical progress.

[0096] The above embodiments are merely used for illustrating the technical concept and features of the present invention, and the purpose thereof lies in allowing those who are familiar to this technique to understand and implement the contents of the present invention, without limiting the scope of protection of the present invention; and any variations or modifications made according to the spirit of the present invention should all be included within the scope of the present invention.