IP Library Granted Patent US 8,097,309
Granted Patent B2
US 8,097,309 · App. 12/819,048 · Granted Jan 17, 2012

Liquid crystal composition and liquid crystal display device

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Quick Facts
Patent No.
US 8,097,309
App. No.
12/819,048
Granted
Jan 17, 2012
Kind
B2
Abstract

The subject is to provide a liquid crystal composition that satisfies at least one characteristic among 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 negatively large dielectric anisotropy, a large specific resistance, a high stability to ultraviolet light and a high stability to heat, or that is suitably balanced regarding two or more characteristics. The other subject is to provide an AM device that has a short response time, a high voltage holding ratio, a high contrast ratio, a long service life and so forth. The invention provides a liquid crystal composition that has negative dielectric anisotropy, including a specific compound having a negatively large dielectric anisotropy as a first component and a two-ring compound having a small viscosity as a second component, and may optionally including a specific compound having a small viscosity as a third component and/or a specific compound having a negatively large dielectric anisotropy as a fourth component, and provides a liquid crystal display device containing the composition.

Claims (28)

1. A liquid crystal composition that has negative dielectric anisotropy, 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 , R 2 , R 3 and R 4 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons, alkenyl having 2 to 12 carbons, alkenyloxy having 2 to 11 carbons, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine; X 1 and X 2 are each independently hydrogen, fluorine or chlorine; X 3 and X 4 are each independently fluorine or chlorine; Z 1 and Z 2 are each independently a single bond, ethylene, methyleneoxy, oxymethylene, carbonyloxy or oxycarbonyl; 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 formula (1-1) and formula (1-2):

wherein R 1 and R 2 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons, alkenyl having 2 to 12 carbons, alkenyloxy having 2 to 11 carbons, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine; X 1 and X 2 are each independently hydrogen, fluorine or chlorine; and X 3 and X 4 are each independently fluorine or chlorine.

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

wherein R 3 , R 4 , R 5 and R 6 are each independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons, alkenyl having 2 to 12 carbons, alkenyloxy having 2 to 11 carbons, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine.

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

5. The liquid crystal composition according to claim 1 , wherein the ratio of the first component is in the range of approximately 5% to approximately 70% by weight and the ratio of the second component is in the range of approximately 25% to approximately 90% by weight, based on the total weight of the liquid crystal composition.

6. The liquid crystal composition according to claim 1 , further comprising at least one compound selected from the group of compounds represented by formula (3-1) and formula (3-2) as a third component:

wherein R 7 , R 8 , R 9 and R 10 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; X 5 and X 6 are each independently fluorine or chlorine; Y 1 is hydrogen or methyl; the ring A is independently 1,4-cyclohexylene in which arbitrary —CH 2 — may be nonadjacently replaced by —O— or —S—, or 1,4-phenylene in which arbitrary hydrogen may be replaced by fluorine or chlorine; Z 3 and Z 4 are each independently a single bond, ethylene, methyleneoxy or carbonyloxy; and n is 1, 2 or 3.

7. The liquid crystal composition according to claim 6 , wherein the third component is at least one compound selected from the group of compounds represented by formula (3-1-1) to formula (3-1-14) and formula (3-2-1) to formula (3-2-5):

wherein R 7 , R 8 , R 9 and R 10 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.

8. The liquid crystal composition according to claim 6 , wherein the ratio of the third component is in the range of approximately 5% to approximately 65% 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 (4) as a fourth component:

wherein R 11 and R 12 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; the ring B and the ring C are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene; the ring C is 1,4-phenylene when p is 1; Z 5 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; and p is 1, 2 or 3.

10. The liquid crystal composition according to claim 9 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-1) to formula (4-11):

wherein R 11 and R 12 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.

11. The liquid crystal composition according to claim 10 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-3), formula (4-5) or formula (4-11).

12. The liquid crystal composition according to claim 9 , wherein the ratio of the fourth component is in the range of approximately 5% to approximately 60% by weight based on the total weight of the liquid crystal composition.

13. The liquid crystal composition according to claim 6 , further comprising at least one compound selected from the group of compounds represented by formula (4) as a fourth component:

wherein R 11 and R 12 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; the ring B and the ring C are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene; the ring C is 1,4-phenylene when p is 1; Z 5 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; and p is 1, 2 or 3.

14. The liquid crystal composition according to claim 13 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-1) to formula (4-11):

wherein R 11 and R 12 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.

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 (4-3), formula (4-5) and formula (4-11).

16. The liquid crystal composition according to claim 13 , wherein the ratio of the fourth component is in the range of approximately 5% to approximately 60% by weight based on the total weight of the liquid crystal composition.

17. 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 −2 or less.

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

19. The liquid crystal display device according to claim 18 , wherein an operating mode of the liquid crystal display device is a VA mode, an IPS 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 Jun 18, 2010
From: KAWASAKI, SUBARU; HATTORI, NORIKATSU
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 024561/0570 →