IP Library Granted Patent US 8,158,219
Granted Patent B2
US 8,158,219 · App. 13/060,054 · Granted Apr 17, 2012

Liquid crystal composition and liquid crystal display device

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,158,219
App. No.
13/060,054
Granted
Apr 17, 2012
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 negative dielectric anisotropy, a large specific resistance, 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 a AM device that has a short response time, a large voltage holding ratio, a large contrast ratio, a long service life and so forth, wherein the liquid crystal composition has negative dielectric anisotropy and includes a two-ring compound having a large negative dielectric anisotropy and having at least three fluorines at the lateral positions as a first component, a specific two-ring or three-ring compound having a pyran ring as a second component, a specific compound having a small viscosity as a third component and a specific compound having a large negative dielectric anisotropy as a fourth component, and the liquid crystal display device contains this composition.

Claims (30)

1. A liquid crystal composition that has negative dielectric anisotropy and includes at least one compound selected from the group of compounds represented by formula (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 and R 2 are 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; R 3 and R 4 are 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

and at least one of the rings A is

X 1 , X 2 , X 3 and X 4 are independently hydrogen, fluorine or chlorine, and at least three of X 1 , X 2 , X 3 and X 4 are fluorine; Z 1 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; and k is 1, 2 or 3.

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 (1-3):

wherein R 1 and R 2 are 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.

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 a mixture of at least one compound selected from the group of compounds represented by formula (1-1) and 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 (2-7):

wherein R 3 and R 4 are 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.

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 (2-4) to formula (2-7).

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

8. The liquid crystal composition according to claim 1 , further including 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 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 independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene; Z 2 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; and m is 1, 2 or 3.

9. The liquid crystal composition according to claim 8 , wherein the third component is at least one compound selected from the group of compounds represented by formula (3-1) to formula (3-11):

wherein R 5 and R 6 are 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.

10. The liquid crystal composition according to claim 8 , wherein the ratio of the third component is in the range of 10% by weight to 80% by weight based on the total weight of the liquid crystal composition.

11. The liquid crystal composition according to claim 1 , further including at least one compound selected from the group of compounds represented by formula (4) as a fourth component:

wherein R 7 and R 8 are 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 D is independently 1,4-cyclohexylene or 1,4-phenylene; Z 3 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; X 5 and X 6 are independently fluorine or chlorine; and n is 1, 2 or 3.

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

wherein R 7 and R 8 are 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.

13. The liquid crystal composition according to claim 11 , wherein the ratio of the fourth component is in the range of 5% by weight to 40% 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 70° C. or higher, the optical anisotropy (25° C.) at a wavelength of 589 nanometers is 0.08 or more, and the dielectric anisotropy (25° C.) at a frequency of 1 kHz is −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.

17. The liquid crystal composition according to claim 8 , further including at least one compound selected from the group of compounds represented by formula (4) as a fourth component:

wherein R 7 and R 8 are 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 D is independently 1,4-cyclohexylene or 1,4-phenylene; Z 3 is independently a single bond, ethylene, methyleneoxy or carbonyloxy; X 5 and X 6 are independently fluorine or chlorine; and n is 1, 2 or 3.

18. The liquid crystal composition according to claim 17 , wherein the fourth component is at least one compound selected from the group of compounds represented by formula (4-1) to formula (4-9):

wherein R 7 and R 8 are 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.

19. The liquid crystal composition according to claim 17 , wherein the ratio of the fourth component is in the range of 5% by weight to 40% by weight based on the total weight of the liquid crystal composition.

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 21, 2011
From: HATTORI, NORIKATSU; SAITO, MASAYUKI; KAWASAKI, SUBARU; FUJITA, HIROAKI
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 025816/0727 →