IP Library Granted Patent US 7,914,860
Granted Patent B2
US 7,914,860 · App. 12/293,542 · Granted Mar 29, 2011

Liquid crystal composition and liquid crystal display device

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Quick Facts
Patent No.
US 7,914,860
App. No.
12/293,542
Granted
Mar 29, 2011
Kind
B2
Abstract

A liquid crystal composition is provided that has a wide temperature range of a nematic phase, has a suitable optical anisotropy, has a large negative dielectric anisotropy and has a large specific resistance, and a liquid crystal composition is provided that can increase an optical anisotropy and has a low minimum temperature of a nematic phase, preferably −20° C. or less, while satisfying the aforementioned characteristics. A liquid crystal display device containing the liquid crystal composition is also provided. The liquid crystal composition of the invention has a negative dielectric anisotropy and contains a liquid crystal compound having terphenyl having one or two fluorines replacing hydrogen as a first component and a liquid crystal compound having phenylene having two halogens replacing hydrogens as a second component. The liquid crystal display device of the invention contains the liquid crystal composition.

Claims (48)

1. A liquid crystal composition having a negative dielectric anisotropy comprising two components, wherein the first component is at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3), and the second component is at least one compound selected from the group of compounds represented by formulas (2-1) to (2-3):

wherein in formulas (1-1) to (1-3) and formulas (2-1) to (2-3),

R 1 and R 3 are each independently alkyl or alkenyl;

R 2 , R 4 and R 5 are each independently alkyl, alkenyl or alkoxy;

ring B, ring C and ring D are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene;

Z 1 , Z 2 and Z 3 are each independently a single bond, —(CH 2 ) 2 —, —CH 2 O— or —OCH 2 —; and

one of X 1 and X 2 is fluorine and the other thereof is chlorine.

2. A liquid crystal composition having a negative dielectric anisotropy comprising two components, wherein the first component is at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3), and the second component is at least one compound selected from the group of compounds represented by formulas (2-1-1), (2-1-2), (2-2-1), (2-2-2), (2-3-1) and (2-3-2):

wherein in formulas (1-1) to (1-3) and formulas (2-1-1), (2-1-2), (2-2-1), (2-2-2), (2-3-1) and (2-3-2),

R 1 and R 3 are each independently alkyl or alkenyl;

R 2 , R 4 and R 5 are each independently alkyl, alkenyl or alkoxy;

ring B and ring C are each independently 1,4-cyclohexylene or 1,4-phenylene; and

Z 2 is independently a single bond, —(CH 2 ) 2 —, —OCH 2 — or —CH 2 O—.

3. The liquid crystal composition according to claim 2 , wherein the first component is at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3), and the second component is a mixture of at least one compound selected from the group of compounds represented by formulas (2-1-1) and (2-1-2) and at least one compound selected from the group of compounds represented by formulas (2-2-1), (2-2-2), (2-3-1) and (2-3-2).

4. The liquid crystal composition according to claim 2 , wherein the composition comprises at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3) as the first component, and at least one compound selected from the group of compounds represented by formulas (2-1-1), (2-1-2), (2-2-1), (2-2-2), (2-3-1) and (2-3-2), in which Z 2 is a single bond, as the second component.

5. A liquid crystal composition having a negative dielectric anisotropy comprising two components, wherein the first component is at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3), and the second component is at least one compound selected from the group of compounds represented by formulas (2-1-1-1), (2-1-2-1), (2-2-1-1), (2-2-2-1), (2-3-1-1) and (2-3-2-1):

wherein in formulas (1-1) to (1-3) and formulas (2-1-1-1), (2-1-2-1), (2-2-1-1), (2-2-2-1), (2-3-1-1) and (2-3-2-1),

R 1 and R 3 are each independently alkyl or alkenyl;

R 2 , R 4 and R 5 are each independently alkyl, alkenyl or alkoxy; and

ring B is independently 1,4-cyclohexylene or 1,4-phenylene.

6. The liquid crystal composition according to claim 1 , wherein the first component is at least one compound selected from the group of compounds represented by formulas (1-1) and (1-2).

7. The liquid crystal composition according to claim 1 , wherein the first component is at least one compound selected from the group of compounds represented by formula (1-1).

8. The liquid crystal composition according to claim 1 , wherein a content ratio of the first component is from 5 to 40% by weight, and a content ratio of the second component is from 60 to 95% by weight, based on the total weight of the liquid crystal compounds.

9. The liquid crystal composition according to claim 2 , wherein the liquid crystal compound component comprises only at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3) as the first component and at least one compound selected from the group of compounds represented by formulas (2-1-1), (2-1-2), (2-2-1), (2-2-2), (2-3-1) and (2-3-2) as the second component.

10. The liquid crystal composition according to claim 1 , wherein the composition further comprises, in addition to the first component and the second component, at least one compound selected from the group of compounds represented by formula (3) as a third component:

wherein in formula (3),

R 6 is independently alkyl or alkenyl;

R 7 is independently alkyl, alkenyl or alkoxy;

ring E and ring G are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene; and

P is 0 or 1.

11. The liquid crystal composition according to claim 10 , wherein the third component is at least one compound selected from the group of compounds represented by formulas (3-1) to (3-13):

wherein in formulas (3-1) to (3-13),

R 6 is independently alkyl or alkenyl; and

R 7 is independently alkyl, alkenyl or alkoxy.

12. The liquid crystal composition according to claim 11 , wherein the liquid crystal compound component comprises only at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3) as the first component, at least one compound selected from the group of compounds represented by formulas (2-1), (2-2) and (2-3) as the second component, and at least one compound selected from the group of compounds represented by formulas (3-1) to (3-13) as the third component.

13. The liquid crystal composition according to claim 11 , wherein the third component is at least one compound selected from the group of compounds represented by formulas (3-1) to (3-5).

14. The liquid crystal composition according to claim 11 , wherein the third component is at least one compound selected from the group of compounds represented by formulas (3-6) to (3-13).

15. The liquid crystal composition according to claim 10 , wherein a content ratio of the first component is from 2 to 30% by weight, a content ratio of the second component is from 40 to 90% by weight, and a content ratio of the third component is from 3 to 38% by weight, based on the total weight of the liquid crystal compounds.

16. The liquid crystal composition according to claim 10 , wherein the composition further comprises, in addition to the first component, the second component and the third component, at least one compound selected from the group of compounds represented by formulas (4-1) to (4-4) as a fourth component:

wherein in formulas (4-1) to (4-4),

R 8 is independently alkyl; and

R 9 is independently alkyl or alkoxy.

17. The liquid crystal composition according to claim 16 , wherein the first component is at least one compound selected from the group of compounds represented by formulas (1-1) to (1-3), the second component is at least one compound selected from the group of compounds represented by formulas (2-1), (2-2) and (2-3), the third component is at least one compound selected from the group of compounds represented by formulas (3-1) to (3-5), and the fourth component is at least one compound selected from the group of compounds represented by formulas (4-1) to (4-3).

18. The liquid crystal composition according to claim 16 , wherein a content ratio of the first component is from 2 to 30% by weight, a content ratio of the second component is from 10 to 85% by weight, a content ratio of the third component is from 3 to 38% by weight, and a content ratio of the fourth component is from 5 to 50% by weight, based on the total weight of the liquid crystal compounds.

19. The liquid crystal composition according to claim 1 , wherein the composition has an optical anisotropy in a range of from 0.10 to 0.20.

20. The liquid crystal composition according to claim 1 , wherein the composition has a dielectric anisotropy in a range of from −5.0 to −2.0.

21. A liquid crystal display device comprising the liquid crystal composition according to claim 1 .

22. The liquid crystal display device according to claim 21 , wherein the liquid crystal display device has an operation mode of a VA mode or an IPS mode and a driving mode of an active matrix mode.

Assignments (3)
CHANGE OF NAME Recorded Jun 1, 2012
From: CHISSO PETROCHEMICAL CORPORATION
To: JNC PETROCHEMICAL CORPORATION
Reel/Frame 028300/0565 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2011
From: CHISSO CORPORATION
To: JNC CORPORATION
Reel/Frame 026207/0653 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2008
From: FUJITA, HIROAKI; HATTORI, NORIKATSU
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 021556/0685 →