Liquid crystal composition and liquid crystal display device

Patent metadata

Field	Value
Publication number	US-2016122301-A1
Application number	US-201414893938-A
Country	US
Kind code	A1
Filing date	Jun 9, 2014
Priority date	Jun 26, 2013
Publication date	May 5, 2016
Grant date	—

Abstract

A liquid crystal composition satisfying at least one of characteristics such as a high maximum temperature of a nematic phase, a low minimum temperature of the 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 a liquid crystal composition having a suitable balance regarding at least two of the characteristics.
The liquid crystal composition contains a compound contributing to the high stability to heat or ultraviolet light, and has a negative dielectric anisotropy and a nematic phase. The composition contains a specific compound having a large negative dielectric anisotropy as a first component, and may contain a specific compound having the high maximum temperature or the small viscosity as a second component.

First claim

1 . A liquid crystal composition that has a negative dielectric anisotropy and a nematic phase, and contains at least one compound selected from the group of compounds represented by formula (1):

wherein, in formula (1), R 1 , R 2 , R 3 and R 4 are independently hydrogen or alkyl having 1 to 15 carbons.

2 . The liquid crystal composition according to claim 1 , wherein a ratio of the compound represented by formula (1) is in the range of 0.005% by weight to 1% by weight based on the weight of the liquid crystal composition.

3 . The liquid crystal composition according to claim 1 , containing at least one compound selected from the group of compounds represented by formula (2) as a first component:

wherein, in formula (2), 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 alkenyloxy having 2 to 12 carbons; ring A and ring C are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 1,4-phenylene in which at least one of hydrogen is replaced by fluorine or chlorine, or tetrahydropyran-2,5-diyl; ring B is 2,3-difluoro-1,4-phenylene, 2-chloro-3-fluoro-1,4-phenylene, 2,3-difluoro-5-methyl-1,4-phenylene, 3,4,5-trifluoronaphthalene-2,6-diyl or 7,8-difluorochroman-2,6-diyl; Z 1 and Z 2 are independently a single bond, ethylene, methyleneoxy or carbonyloxy; and a is 1, 2 or 3, b is 0 or 1, and a sum of a and b is 3 or less.

4 . The liquid crystal composition according to claim 3 , containing at least one compound selected from the group of compounds represented by formula (2-1) to formula (2-19) as the first component:

wherein, in formula (2-1) to formula (2-19), 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 alkenyloxy having 2 to 12 carbons.

5 . The liquid crystal composition according to claim 3 , wherein a ratio of the first component is in the range of 10% by weight to 90% by weight based on the weight of the liquid crystal composition.

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

wherein, in formula (3), 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 at least one of hydrogen is replaced by fluorine; ring D and ring E are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; Z 3 is a single bond, ethylene or carbonyloxy; and c is 1, 2 or 3.

7 . The liquid crystal composition according to claim 6 , containing at least one compound selected from the group of compounds represented by formula (3-1) to formula (3-13) as the second component:

wherein, in formula (3-1) to formula (3-13), 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 at least one of hydrogen is replaced by fluorine.

8 . The liquid crystal composition according to claim 6 , wherein a ratio of the second component is in the range of 10% by weight to 90% by weight based on the weight of the liquid crystal composition.

9 . The liquid crystal composition according to claim 1 , wherein a maximum temperature of the nematic phase is 70° C. or higher, an optical anisotropy (measured at 25° C.) at a wavelength of 589 nanometers is 0.08 or more, and dielectric anisotropy (measured at 25° C.) at a frequency of 1 kHz is −2 or less.

10 . A liquid crystal display device, including the liquid crystal composition according to claim 1 .

11 . The liquid crystal display device according to claim 10 , wherein an operating mode in the liquid crystal display device includes an IPS mode, a VA mode, a PSA mode, an FFS mode or an FPA mode, and a driving mode in the liquid crystal display device includes an active matrix mode.

12 . (canceled)

13 . The liquid crystal composition according to claim 3 , containing at least one compound selected from the group of compounds represented by formula (3) as a second component:

wherein, in formula (3), 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 at least one of hydrogen is replaced by fluorine; ring D and ring E are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; Z 3 is a single bond, ethylene or carbonyloxy; and c is 1, 2 or 3.

Assignees

• Jnc Corp
• Jnc Petrochemical Corp

Inventors

• Furusato Yoshimasa
• Saito Masayuki

Classifications

• C09K19/3402

  having oxygen as hetero atom (sugars C09K19/0422) · CPC title

• C09K19/3066

  in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers · CPC title

• C07D211/46 Primary

  having a hydrogen atom as the second substituent in position 4 · CPC title

• C09K19/54

  Additives having no specific mesophase {characterised by their chemical composition} · CPC title

• C09K2019/3425

  Six-membered ring with oxygen(s) in fused, bridged or spiro ring systems · CPC title