IP Library Granted Patent US 8,398,886
Granted Patent B2
US 8,398,886 · App. 12/860,695 · Granted Mar 19, 2013

Liquid crystal composition and liquid crystal display device

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Quick Facts
Patent No.
US 8,398,886
App. No.
12/860,695
Granted
Mar 19, 2013
Kind
B2
Abstract

The invention provides a liquid crystal composition that includes a specific compound having a negatively large dielectric anisotropy as a first component and a specific compound having a negatively large dielectric anisotropy as a second component, that optionally includes a specific compound having a high maximum temperature or a small viscosity as a third component and a specific compound having a negatively large dielectric anisotropy as a fourth component, and that has negative dielectric anisotropy, and provides a liquid crystal display device containing this composition.

Claims (25)

1. A liquid crystal composition that has negative dielectric anisotropy and comprises 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, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine; the ring A is independently 1,4-cyclohexylene or 1,4-phenylene; the ring B is independently 1,4-cyclohexylene, 1,4-phenylene in which arbitrary hydrogen may be replaced by fluorine or chlorine, or tetrahydropyran-2,5-diyl, and at least one of the ring B is tetrahydropyran-2,5-diyl; Z 1 is independently ethylene or methyleneoxy; Z 2 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; m and n are each independently 1, 2 or 3; and one of X 1 and X 2 is fluorine and the other is chlorine.

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) to formula (1-12):

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, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine.

3. 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 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, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine.

4. The liquid crystal composition according to claim 1 , wherein the ratio of the first component is in the range of approximately 5% to approximately 60% by weight and the ratio of the second component is in the range of approximately 5% to approximately 40% by weight, based on the total weight of the liquid crystal composition.

5. 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 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, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine; the ring C and the ring D are each independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene; Z 3 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; and p is 1, 2 or 3.

6. The liquid crystal composition according to claim 5 , 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 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, or alkenyl having 2 to 12 carbons in which arbitrary hydrogen is replaced by fluorine.

7. The liquid crystal composition according to claim 5 , wherein the ratio of the third component is in the range of approximately 25% to approximately 70% by weight based on the total weight of the liquid crystal composition.

8. The liquid crystal composition according to claim 1 , further comprising at least one compound selected from the group of compounds represented by formula (4-1) and formula (4-2) as a fourth 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; the ring E, the ring F and the ring G are each independently 1,4-cyclohexylene or 1,4-phenylene in which arbitrary hydrogen may be replaced by fluorine; Z 4 and Z 5 are each independently a single bond, ethylene, methyleneoxy or carbonyloxy; q and r are each independently 0, 1, 2 or 3, and the sum of q and r is 3 or less; and s is 1, 2 or 3.

9. The liquid crystal composition according to claim 5 , further comprising at least one compound selected from the group of compounds represented by formula (4-1) and formula (4-2) as a fourth 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; the ring E, the ring F and the ring G are each independently 1,4-cyclohexylene or 1,4-phenylene in which arbitrary hydrogen may be replaced by fluorine; Z 4 and Z 5 are each independently a single bond, ethylene, methyleneoxy or carbonyloxy; q and r are each independently 0, 1, 2 or 3, and the sum of q and r is 3 or less; and s is 1, 2 or 3.

10. The liquid crystal composition according to claim 8 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-1-1) to formula (4-1-9) and formula (4-2-1) to formula (4-2-5):

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.

11. 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 (4-1-1) to formula (4-1-9) and formula (4-2-1) to formula (4-2-5):

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.

12. The liquid crystal composition according to claim 8 , wherein the ratio of the fourth component is in the range of approximately 5% to approximately 50% by weight based on the total weight of the liquid crystal composition.

13. The liquid crystal composition according to claim 9 , wherein the ratio of the fourth component is in the range of approximately 5% to approximately 50% by weight based on the total weight of the liquid crystal composition.

14. 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.

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

16. The liquid crystal display device according to claim 15 , 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 Aug 20, 2010
From: YANAI, TAKAYOSHI; SAITO, MASAYUKI
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 024867/0819 →