IP Library Granted Patent US 8,133,410
Granted Patent B2
US 8,133,410 · App. 12/673,155 · Granted Mar 13, 2012

Liquid crystal composition and liquid crystal display device

Assignees: JNC Corporation; Chisso Petrochemical Corporation
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Quick Facts
Patent No.
US 8,133,410
App. No.
12/673,155
Granted
Mar 13, 2012
Kind
B2
Abstract

The invention is to provide a liquid crystal composition that satisfies at least one characteristic among the characteristics such as a high maximum temperature of a nematic phase, a low minimum temperature of a nematic phase, a small viscosity, a large optical anisotropy, a large dielectric anisotropy, a large specific resistance, a high stability to ultraviolet light and a high stability to heat, or that is suitably balanced concerning at least two characteristics. The invention is to provide an AM device that has a short response time, a large voltage holding ratio, a large contrast ratio, a long service life and so forth. The invention is to provide a liquid crystal composition having a nematic phase that contains a specific five-membered ring compound having a large optical anisotropy and a large dielectric anisotropy as a first component and a specific compound having a small viscosity as a second component, and a liquid crystal display device containing the composition.

Claims (25)

1. A liquid crystal composition having a nematic phase that comprises at least one compound selected from the group of compounds represented by formulas (1) as a first component and at least one compound selected from the group of compounds represented by formula (2) as a second component:

wherein R 1 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; R 2 and R 3 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons, alkenyl having 2 to 12 carbons or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine; ring A, ring B and ring C are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; Z 1 , Z 2 and Z 3 are each independently a single bond, ethylene, carbonyloxy or difluoromethyleneoxy, wherein at least one of Z 1 , Z 2 and Z 3 is difluoromethyleneoxy; Z 4 and Z 5 are each independently a single bond, ethylene or carbonyloxy; X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 are each independently hydrogen or fluorine; Y 1 is fluorine, chlorine or trifluoromethoxy; and m is 0 or 1.

2. 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) to (1-3):

wherein R 1 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 and X 8 are each independently hydrogen or fluorine; and Y 1 is fluorine, chlorine or trifluoromethoxy.

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 formula (1-1).

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

wherein R 2 and R 3 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons, alkenyl having 2 to 12 carbons or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine.

5. The liquid crystal composition according to claim 4 , wherein the second component is at least one compound selected from the group of compounds represented by formula (2-1).

6. The liquid crystal composition according to claim 4 , wherein the second component is at least one compound selected from the group of compounds represented by formula (2-6).

7. The liquid crystal composition according to claim 4 , wherein the second component is a mixture of at least one compound selected from the group of compounds represented by formula (2-1), and at least one compound selected from the group of compounds represented by formula (2-4).

8. The liquid crystal composition according to claim 4 , wherein the second component is a mixture of at least one compound selected from the group of compounds represented by formula (2-1), and at least one compound selected from the group of compounds represented by formula (2-6).

9. The liquid crystal composition according to claim 1 , wherein the ratio of the first component is in the range of 5% to 30% by weight, and the ratio of the second component is in the range of 35% to 80% by weight, based on the total weight of the liquid crystal composition.

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

wherein R 1 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; ring D is independently 1,4-cyclohexylene, 1,3-dioxane-2,5-diyl, 1,4-phenylene, 3-fluoro-1,4-phenylene, 3,5-difluoro-1,4-phenylene or 2,5-pyrimidine; Z 1 is a single bond, ethylene, carbonyloxy or difluoromethyleneoxy; X 1 and X 2 are each independently hydrogen or fluorine; Y 1 is fluorine, chlorine or trifluoromethoxy; and n is 1, 2 or 3.

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 (3-17):

wherein R 4 is alkyl having 1 to 12 carbons or alkenyl having 2 to 12 carbons.

12. 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 formula (3-9).

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 formula (3-11).

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 formula (3-17).

15. The liquid crystal composition according to claim 11 , wherein the third component is a mixture of at least one compound selected from the group of compounds represented by formula (3-6), and at least one compound selected from the group of compounds represented by formula (3-11).

16. The liquid crystal composition according to claim 10 , wherein the ratio of the third component is in the range of 5% to 50% by weight based on the total weight of the liquid composition.

17. The liquid crystal composition according to claim 1 , wherein the composition has a maximum temperature of a nematic phase of 70° C. or more, an optical anisotropy (25° C.) of 0.08 or more at a wavelength of 589 nm, and a dielectric anisotropy (25° C.) of 2 or more at a frequency of 1 kHz.

18. A liquid crystal display device that comprises the liquid crystal composition according to claim 1 .

19. A liquid crystal display device according to claim 18 , wherein an operating mode of the liquid crystal display device is a TN mode, an OCB mode or an IPS mode, and a driving mode of the liquid crystal display device is an active matrix mode.

20. A liquid crystal display device according to claim 18 , wherein an operating mode of the liquid crystal display device is a PSA mode and a driving mode of the liquid crystal display device is 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 Feb 11, 2010
From: SAITO, MASAYUKI; KIBE, SHIGERU
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 023943/0437 →
Priority Claims (2)
JP 2007-219689 · Aug 27, 2007 · national
WO PCT/JP2008/064804 · Aug 20, 2008 · international
Continuity (1)
Related Publication 20110095228A1 · Apr 28, 2011