IP Library Granted Patent US 9,951,277
Granted Patent B2
US 9,951,277 · App. 15/121,383 · Granted Apr 24, 2018

Liquid crystal compound having 1,1,3,3-tetrafluoroallyloxy group, liquid crystal composition and liquid crystal display device

Inventors: Akihiro Takata (Chiba, JP); Takahiro Kubo (Chiba, JP)
Assignees: JNC CORPORATION; JNC PETROCHEMICAL CORPORATION
C09K19/3458C07C43/225C07D213/30C07D239/26C07D309/06C07D319/06C07D405/04C07D493/08C09K19/20C09K19/3028C07C2101/14C09K2019/0444C09K2019/0466C09K2019/123C09K2019/124C09K2019/301C09K2019/308C09K2019/3016C09K2019/3019C09K2019/3025C09K2019/3077C09K2019/3083C09K2019/3422
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 9,951,277
App. No.
15/121,383
Granted
Apr 24, 2018
Kind
B2
Abstract

To show a liquid crystal compound satisfying at least one of physical properties such as a high stability to heat, light or the like, a high clearing point, a low minimum temperature of a liquid crystal phase, a small viscosity, a suitable optical anisotropy, a large dielectric anisotropy, a suitable elastic constant and an excellent compatibility with other liquid crystal compounds, a liquid crystal composition containing the compound and a liquid crystal display device including the composition. A compound represented by formula (1): wherein, in formula (1), for example, R 1 is alkyl having 1 to 15 carbons; ring A 1 and ring A 2 are 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 1,4-phenylene in which at least one piece of hydrogen is replaced by halogen, tetrahydropyran-2,5-diyl or 1,3-dioxane-2,5-diyl; Z 1 and Z 2 are a single bond or —CF 2 O—; L 1 , L 2 and L 3 are halogen or hydrogen; and a is 0 to 3.

Claims (65)

1. A compound, represented by formula (1):

wherein, in formula (1),

R 1 is alkyl having 1 to 15 carbons, and in the alkyl, at least one piece of —CH 2 — may be replaced by —O—, and at least one piece of —CH 2 CH 2 — may be replaced by —CH═CH—, and in the groups, at least one piece of hydrogen may be replaced by halogen;

ring A 1 and ring A 2 are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 1,4-phenylene in which at least one piece of hydrogen is replaced by halogen, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl, 2,6,7-trioxabicyclo[2.2.2]octane-1,4-diyl, pyrimidine-2,5-diyl or pyridine-2,5-diyl;

Z 1 and Z 2 are independently a single bond, —CH 2 CH 2 —, —C≡C—, —CH═CH—, —CF═CF—, —CF 2 O—, —OCF 2 —, —CH 2 O—, —OCH 2 —, —COO— or —OCO—;

L 1 , L 2 and L 3 are independently hydrogen or halogen; and

a is 0, 1, 2 or 3.

2. The compound according to claim 1 , wherein, in formula (1), R 1 is alkyl having 1 to 15 carbons, alkenyl having 2 to 15 carbons, alkoxy having 1 to 14 carbons or alkenyloxy having 2 to 14 carbons.

3. The compound according to claim 1 , wherein, in formula (1), Z 1 and Z 2 are independently a single bond, —CH 2 CH 2 —, —C≡C—, —CH═CH—, —CF 2 O— or —COO—.

4. The compound according to claim 1 , represented by any one of formulas (1-1) to (1-4):

wherein, in formulas (1-1) to (1-4),

ring A 1 , ring A 2 , ring A 3 and ring A 4 are independently 1,4-cyclohexylene, 1,4-phenylene, 1,4-phenylene in which at least one piece of hydrogen is replaced by halogen, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl or 2,6,7-trioxabicyclo[2.2.2]octane-1,4-diyl;

Z 1 , Z 2 , Z 3 and Z 4 are independently a single bond, —CH 2 CH 2 —, —CH═CH—, —CF 2 O— or —COO—;

R 1 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons; and

L 1 and L 2 are independently hydrogen or halogen.

5. The compound according to claim 4 ,

wherein, in formulas (1-1) to (1-4),

ring A 1 , ring A 2 , ring A 3 and ring A 4 are independently 1,4-cyclohexylene, 1,4-phenylene, 1,4-phenylene in which at least one piece of hydrogen is replaced by fluorine or chlorine, tetrahydropyran-2,5-diyl or 1,3-dioxane-2,5-diyl;

Z 1 , Z 2 , Z 3 and Z 4 are independently a single bond, —CH 2 CH 2 —, —CH═CH— or —CF 2 O—;

R 1 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons; and

L 1 and L 2 are independently hydrogen or fluorine

6. The compound according to claim 1 , represented by any one of formulas (1-5) to (1-12):

wherein, in formulas (1-5) to (1-12),

ring A 1 and ring A 2 are independently 1,4-cyclohexylene, tetrahydropyran-2,5-diyl or 1,3-dioxane-2,5-diyl;

Z 1 and Z 2 are independently a single bond or —CF 2 O—;

R 1 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons; and

L 1 , L 2 , L 3 , L 4 , L 5 , L 6 , L 7 and L 8 are independently hydrogen or fluorine.

7. The compound according to claim 1 , represented by any one of formulas (1-13) to (1-23):

wherein, in formulas (1-13) to (1-23),

R 1 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons; and

L 1 , L 2 , L 3 , L 4 , L 5 , L 6 , L 7 and L 8 are independently hydrogen or fluorine.

8. A liquid crystal composition, containing at least one of the compounds according to claim 1 .

9. The liquid crystal composition according to claim 8 , further containing at least one compound selected from the group of compounds represented by formulas (2) to (4):

wherein, in formulas (2) to (4),

R 11 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one piece of hydrogen may be replaced by fluorine, and at least one piece of —CH 2 — may be replaced by —O—;

X 11 is fluorine, chlorine, —OCF 3 , —OCHF 2 , —CF 3 , —CHF 2 , —CH 2 F, —OCF 2 CHF 2 or —OCF 2 CHFCF 3 ;

ring B 1 , ring B 2 and ring B 3 are independently 1,4-cyclohexylene, 1,4-phenylene in which at least one piece of hydrogen may be replaced by fluorine, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl or pyrimidine-2,5-diyl;

Z 11 , Z 12 and Z 13 are independently a single bond, —CH 2 CH 2 —, —CH═CH—, —C≡C—, —COO—, —CF 2 O—, —OCF 2 —, —CH 2 O— or —(CH 2 ) 4 —; and

L 11 and L 12 are independently hydrogen or fluorine.

10. The liquid crystal composition according to claim 8 , further containing at least one compound selected from the group of compounds represented by formula (5):

wherein, in formula (5),

R 12 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one piece of hydrogen may be replaced by fluorine, and at least one piece of —CH 2 — may be replaced by —O—;

X 12 is —C≡N or —C≡C—C≡N;

ring C 1 is 1,4-cyclohexylene, 1,4-phenylene in which at least one piece of hydrogen may be replaced by fluorine, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl or pyrimidine-2,5-diyl;

Z 14 is a single bond, —CH 2 CH 2 —, —C≡C—, —COO—, —CF 2 O—, —OCF 2 — or —CH 2 O—;

L 13 and L 14 are independently hydrogen or fluorine; and

i is 1, 2, 3 or 4.

11. The liquid crystal composition according to claim 8 , further containing at least one compound selected from the group of compounds represented by formulas (6) to (12):

wherein, in formulas (6) to (12),

R 13 and R 14 are independently alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one piece of —CH 2 — may be replaced by —O—, and at least one piece of hydrogen may be replaced by fluorine;

R 15 is hydrogen, fluorine, alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one piece of —CH 2 — may be replaced by —O—, and at least one piece of hydrogen may be replaced by fluorine;

S 11 is hydrogen or methyl;

X is —CF 2 —, —O— or —CHF—;

ring D 1 , ring D 2 , ring D 3 and ring D 4 are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene in which at least one piece of hydrogen may be replaced by fluorine, tetrahydropyran-2,5-diyl or decahydronaphthalene-2,6-diyl;

ring D 5 and ring D 6 are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, tetrahydropyran-2,5-diyl or decahydronaphthalene-2,6-diyl;

Z 15 , Z 16 , Z 17 and Z 18 are independently a single bond, —CH 2 CH 2 —, —COO—, —CH 2 O—, —OCF 2 — or —OCF 2 CH 2 CH 2 —;

L 15 and L 16 are independently fluorine or chlorine; and

j, k, m, n, p, q, r and s are independently 0 or 1, a sum of k, m, n and p is 1 or 2, a sum of q, r and s is 0, 1, 2 or 3, and t is 1, 2 or 3.

12. The liquid crystal composition according to claim 8 , further containing at least one compound selected from the group of compounds represented by formulas (13) to (15):

wherein, in formulas (13) to (15),

R 16 and R 17 are independently alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one piece of —CH 2 — may be replaced by —O—, and at least one piece of hydrogen may be replaced by fluorine;

ring E 1 , ring E 2 , ring E 3 and ring E 4 are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene or pyrimidine-2,5-diyl; and

Z 19 , Z 20 and Z 21 are independently a single bond, —CH 2 CH 2 —, —CH═CH—, —C≡C— or —COO—.

13. The liquid crystal composition according to claim 8 , further containing at least one selected from a polymerizable compound, an optically active compound, an antioxidant, an ultraviolet light absorber, a light stabilizer, a heat stabilizer and an antifoaming agent.

14. A liquid crystal display device, including the liquid crystal composition according to claim 8 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2025
From: JNC CORPORATION; JNC PETROCHEMICAL CORPORATION
To: JIANGSU HECHENG DISPLAY TECHNOLOGY CO., LTD.
Reel/Frame 072472/0393 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 1, 2016
From: TAKATA, AKIHIRO; KUBO, TAKAHIRO
To: JNC CORPORATION; JNC PETROCHEMICAL CORPORATION
Reel/Frame 039607/0995 →
Priority Claims (1)
JP 2014-033987 · Feb 25, 2014 · national
Continuity (1)
Related Publication 20160362605A1 · Dec 15, 2016