IP Library › Granted Patent US 8,366,964
Granted Patent B2
US 8,366,964 · App. 13/073,730 · Granted Feb 5, 2013

Liquid crystal composition and liquid crystal display device

Inventors: Taketo Maeda (Ichihara, JP); Norikatsu Hattori (Ichihara, JP); Hiroaki Fujita (Ichihara, JP)
Assignees: JNC Corporation; JNC Petrochemical Corporation
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Quick Facts
Patent No.
US 8,366,964
App. No.
13/073,730
Granted
Feb 5, 2013
Kind
B2
Abstract

The invention is to provide a liquid crystal composition that satisfies at least one of characteristics such as a high maximum temperature of a nematic phase, a low minimum temperature of a nematic phase, a small viscosity, a suitable optical anisotropy, a large dielectric anisotropy, a large specific resistance, a large elastic constant, a high stability to ultraviolet light and a high stability to heat, or that is suitably balanced regarding at least two of the characteristics; and 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 provides a liquid crystal composition that has a nematic phase and includes a specific three-ring compound having a large dielectric anisotropy as a first component and a specific four-ring compound having a high maximum temperature and a large dielectric anisotropy as a second component, and a liquid crystal display device containing the composition.

Claims (33)

1. A liquid crystal composition having a nematic phase and comprising two components, wherein a first component is at least one compound selected from the group of compounds represented by formula (1), and a second component is at least one compound selected from the group of compounds represented by formula (2):

wherein R 1 and R 2 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; the ring A is 1,4-cyclohexylene, 1,4-phenylene or tetrahydropyran-2,5-diyl; X 1 , X 2 , X 3 , X 4 and X 5 are each independently hydrogen or fluorine; and Y 1 is fluorine, chlorine or trifluoromethoxy.

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 formula (1-1) and formula (1-2):

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

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 2 , wherein the first component is at least one compound selected from the group of compounds represented by formula (1-2).

5. 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 formula (2-1) to formula (2-4):

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

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

7. The liquid crystal composition according to claim 5 , wherein the second component is at least one compound selected from the group of compounds represented by formula (2-3).

8. The liquid crystal composition according to claim 1 , wherein the ratio of the first component is in the range of approximately 5% by weight to approximately 60% by weight and the ratio of the second component is in the range of approximately 5% by weight to approximately 50% by weight, based on the total weight of the liquid crystal composition.

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

wherein R 3 and R 4 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons, alkoxymethyl having 2 to 12 carbons, alkenyl having 2 to 12 carbons, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine; the ring B, the ring C and the ring D are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene or tetrahydropyran-2,5-diyl; Z 1 is independently a single bond, ethylene or carbonyloxy; and m is 0, 1 or 2.

10. The liquid crystal composition according to claim 9 , wherein the third component is at least one compound selected from the group of compounds represented by formula (3-1) to formula (3-13):

wherein R 3 and R 4 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons, alkoxymethyl having 2 to 12 carbons, alkenyl having 2 to 12 carbons, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine.

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 formula (3-1).

12. The liquid crystal composition according to claim 10 , wherein the third component is a mixture of at least one compound selected from the group of compounds represented by formula (3-1) and at least one compound selected from the group of compounds represented by formula (3-7).

13. The liquid crystal composition according to claim 9 , wherein the ratio of the third component is in the range of approximately 5% by weight to approximately 80% by weight based on the total weight of the liquid crystal composition.

14. The liquid crystal composition according to claim 9 , further comprising at least one compound selected from the group of compounds represented by formula (4) as a fourth component:

wherein R 5 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; the ring E is independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, 3,5-difluoro-1,4-phenylene, 1,3-dioxane-2,5-diyl or tetrahydropyran-2,5-diyl; X 6 and X 7 are each independently hydrogen or fluorine; Y 2 is fluorine or chlorine; Z 2 is independently a single bond, ethylene, carbonyloxy or difluoromethyleneoxy; and n is 1 or 2.

15. The liquid crystal composition according to claim 14 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-1) to formula (4-17):

wherein R 5 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons.

16. The liquid crystal composition according to claim 15 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-15).

17. The liquid crystal composition according to claim 15 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-17).

18. The liquid crystal composition according to claim 14 , wherein the ratio of the fourth component is in the range of approximately 5% by weight to approximately 60% by weight based on the total weight of the liquid crystal composition.

19. The liquid crystal composition according to claim 9 , further comprising at least one compound selected from the group of compounds represented by formula (5) as a fifth component:

wherein R 6 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; the ring F is independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene, 3,5-difluoro-1,4-phenylene, 1,3-dioxane-2,5-diyl or tetrahydropyran-2,5-diyl; X 8 and X 9 are each independently hydrogen or fluorine; Y 3 is fluorine or chlorine; and Z 3 is independently a single bond or ethylene.

20. The liquid crystal composition according to claim 19 , wherein the fifth component is at least one compound selected from the group of compounds represented by formula (5-1) to formula (5-5):

wherein R 6 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons.

21. The liquid crystal composition according to claim 19 , wherein the ratio of the fifth component is in the range of approximately 5% by weight to approximately 30% by weight based on the total weight of the liquid crystal composition.

22. The liquid crystal composition according to claim 1 , wherein the maximum temperature of a nematic phase is approximately 70° C. or higher, the optical anisotropy (25° C.) at a wavelength of 589 nanometers is approximately 0.08 or more, and the dielectric anisotropy (25° C.) at a frequency of 1 kHz is approximately 4 or more.

23. A liquid crystal display device containing the liquid crystal composition according to claim 1 .

24. The liquid crystal display device according to claim 23 , wherein an operating mode of the liquid crystal display device is a TN mode, an OCB mode, an IPS mode, an FFS mode or 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 Mar 28, 2011
From: MAEDA, TAKETO; HATTORI, NORIKATSU; FUJITA, HIROAKI
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 026034/0045 →
Priority Claims (1)
JP 2010-101768 · Apr 27, 2010 · national
Continuity (1)
Related Publication 20110260104A1 · Oct 27, 2011