IP Library Granted Patent US 7,407,691
Granted Patent B2
US 7,407,691 · App. 11/085,903 · Granted Aug 5, 2008

Photopolymerizable oxetane derivative and liquid-crystal composition containing it

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Quick Facts
Patent No.
US 7,407,691
App. No.
11/085,903
Granted
Aug 5, 2008
Kind
B2
Abstract

Provided are a liquid-crystal compound and a liquid-crystal composition containing the compound, of which the advantages are that they show nematic hybrid orientation on a rubbed TAC substrate, they are polymerizable in open air and they readily give a polymer having a high degree of polymerization even when exposed to a relatively small total quantity of light. The films formed by photopolymerizing them keep nematic hybrid orientation. The compound is represented by formula (1): wherein R 1 is a hydrogen or an alkyl; R 2 is a hydrogen, —OCF 3 , etc.; A 1 is a 1,4-phenylene, etc.; A 2 and A 3 are independently a 1,4-cyclohexylene, a 1,4-phenylene, etc.; X 1 is a single bond, —O—, etc.; X 2 and X 3 are independently a single bond, —COO—, —C≡C—, —CONH—, etc.; m is an integer of from 0 to 20; and n is 1 or 0.

Claims (25)

1. A compound of a formula (1):

wherein R 1 represents a hydrogen atom or an alkyl group having from 1 to 5 carbon atoms; R 2 represents a hydrogen atom, —NCO, —NCS, —OCHF 2 , —CH 2 F, —OCF 2 CF 2 H, —OCF 2 CHFCF 3 , or —Y 1 —(CF 2 )s-CF 3 , in which Y 1 represents —O—, —S—, —COO—, —OCO—, —CO—, —CH═CH—, or —C≡C—, s indicates an integer of from 0 to 10; A 1 represents a 1,4-phenylene group, or a 1,4-phenylene group in which any hydrogen atom is substituted with a halogen atom, a cyano group, a methyl group, an ethyl group, a methoxy group, a hydroxy group, a formyl group, an acetoxy group, an acetyl group, a carbonylmethyl group, a carbonyltrifluoromethyl group, a difluoromethyl group, or a trifluoromethyl group; A 2 and A 3 each independently represent a 1,4-cyclohexylene group, a 1,4-phenylene group, a pyridine-2,5-diyl group, a pyridazine-3,6-diyl group, a pyrimidine-2,5-diyl group, a naphthalene-2,6-diyl group, a tetrahydronaphthalene-2,6-diyl group, a 1,4-cyclohexylene group in which any hydrogen atom is substituted with a fluorine atom, or a 1,4-phenylene group in which any hydrogen atom is substituted with a halogen atom, a cyano group, a methyl group, an ethyl group, a methoxy group, a hydroxy group, a formyl group, an acetoxy group, an acetyl group, a carbonylmethyl group, a carbonyltrifluoromethyl group, a difluoromethyl group or a trifluoromethyl group; X 1 represents a single bond, —O— or —OCO—; X 2 and X 3 each independently represent a single bond, —CH═CH—COO—, —OOC—CH═CH—, —CH 2 CH 2 —COO—, —OOC—CH 2 CH 2 —, —COO—, —OCO—, —OCH 2 —, —CH 2 O—, —OCF 2 —, —CF 2 O—, —CH 2 CH 2 —, —C≡C—, —NHCO—, or —CONH—; m indicates an integer of from 0 to 20; and n indicates 1 or 0.

2. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —Y 1 —(CF 2 )s—CF 3 , in which Y 1 is —O—, —S—, —COO—, —OCO—, —CO—, —CH═CH—, or —C≡C—, s is an integer of from 0 to 10.

3. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —Y 1 —(CF 2 )s—CF 3 , in which Y 1 is —O—, s is an integer of from 0 to 10; A 1 is a 1,4-phenylene group, or a 1,4-phenylene group in which any hydrogen atom is substituted with a halogen atom, a methyl group, an acetyl group or a trifluoromethyl group; A 2 and A 3 are independently a 1,4-cyclohexylene group, a 1,4-phenylene group, a pyridine-2,5-diyl group, a pyridazine-3,6-diyl group, a pyrimidine-2,5-diyl group, a naphthalene-2,6-diyl group, a tetrahydronaphthalene-2,6-diyl group, or a 1,4-phenylene group in which any hydrogen atom is substituted with a halogen atom, a methyl group, an acetyl group or a trifluoromethyl group; X 1 is a single bond or —O—; X 2 and X 3 are independently a single bond, —CH═CH—COO—, —CH 2 CH 2 —COO—, —COO—, —C≡C—, or —CONH—.

4. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —OCF 3 ; A 1 is a 1,4-phenylene group, or a 1,4-phenylene group in which any hydrogen atom is substituted with a halogen atom, a methyl group, an acetyl group or a trifluoromethyl group; A 2 and A 3 are independently a 1,4-cyclohexylene group, a 1,4-phenylene group, a pyridine-2,5-diyl group, a pyridazine-3,6-diyl group, a pyrimidine-2,5-diyl group, a naphthalene-2,6-diyl group, a tetrahydronaphthalene-2,6-diyl group, or a 1,4-phenylene group in which any hydrogen atom is substituted with a halogen atom, a methyl group, an acetyl group or a trifluoromethyl group; X 1 is a single bond or —O—; X 2 and X 3 are independently a single bond, —CH═CH—COO—, —CH 2 CH 2 —COO—, —COO—, —C≡C—, or —CONH—.

5. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —OCF 3 ; A 1 is a 1,4-phenylene group; A 2 and A 3 are independently a 1,4-phenylene group or a 3-fluoro-1,4-phenylene group; X 1 is a single bond or —O—; X 2 and X 3 are independently a single bond, —CH═CH—COO—, —CH 2 CH 2 —COO—, —COO—,—C≡C—, or —CONH—; m is an integer of from 0 to 8.

6. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —OCF 3 ; A 1 is a 1,4-phenylene group; A 2 and A 3 are independently a 1,4-phenylene group or a 3-fluoro-1,4-phenylene group; X 1 is a single bond or —O—; X 2 and X 3 are independently a single bond, —CH═CH—COO—, —CH 2 CH 2 —COO—, —COO—, or —CONH—; m is an integer of from 0 to 6.

7. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —OCF 3 ; A 1 is a 1,4-phenylene group A 2 a 1,4-phenylene group or a 3-fluoro-1,4-phenylene group; X 1 is a single bond or —O—; X 2 is —CH═CH—COO—, —CH 2 CH 2 —COO—, —COO—, or —CONH—; m is an integer of from 0 to 6; and n is 0.

8. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —OCF 3 ; A 1 is a 1,4-phenylene group; A 2 is a 1,4-phenylene group or a 3-fluoro-1,4-phenylene group; X 1 is a single bond or —O—; X 2 is —COO—; m is an integer of from 0 to 6; and n is 0.

9. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —OCF 3 ; A 1 is a 1,4-phenylene group; A 2 a 1,4-phenylene group or a 3-fluoro-1,4-phenylene group; A 3 is a 1,4-phenylene group; X 1 is a single bond or —O—; X 2 is —CH═CH—COO—, —CH 2 CH 2 —COO—, —COO—, or —CONH—; X 3 is a single bond; m is an integer of from 0 to 6; and n is 1.

10. The compound as claimed in claim 1 , wherein, in formula (1), R 1 is a methyl or ethyl group; R 2 is —OCF 3 ; A 1 , A 2 and A 3 is a 1,4-phenylene group; X 1 is a single bond or —O—; X 2 is —COO—; X 3 is a single bond; m is an integer of from 0 to 6; and n is 1.

11. A liquid-crystal composition containing at least two compounds, in which at least one compound is the compound of claim 1 .

12. The liquid-crystal composition as claimed in claim 11 , wherein all the compounds are polymerizable compounds.

13. The liquid-crystal composition as claimed in claim 11 , wherein at least one compound is the compound of formula (1) and at least one other compound is a polymerizable compound that differs from the compound of claim 1 .

14. The liquid-crystal composition as claimed in claim 11 , wherein all the compounds are the compounds of formula (1).

15. The liquid-crystal composition as claimed in claim 11 , which contains at least one compound of formula (1) and at least one polymerizable compound selected from a group of compounds of formulae (M1), (M2), (M3), (M4) and (M5):

wherein R 5 independently represents a hydrogen atom, a fluorine atom, a chlorine atom, —CN, or an alkyl group having from 1 to 20 carbon atoms; in the alkyl group, any —CH 2 — may be substituted with —O—, —S—, —COO—, —OCO—or —CO—, and any hydrogen may be substituted with a halogen atom; R 6 independently represents a hydrogen atom or an alkyl group having from 1 to 5 carbon atoms; A 4 , A 5 , A 6 and A 7 each independently represent a 1,4-cyclohexylene group, a 1,4-phenylene group, a pyridine-2,5-diyl group, a pyrimidine-2,5-diyl group, a naphthalene-2,6-diyl group, a fluorene-2,7-diyl group, or a 1,4-phenylene group in which any hydrogen atom is substituted with a halogen atom or a cyano group; B 1 independently represents a single bond, a 1,4-phenylene group, a naphthalene-2,6-diyl group, a biphenyl-4,4′-diyl group, a fluorene-2,7-diyl group, a 9-methylfluoren-2,7-diyl group, a 9-ethylfluorene-2,7-diyl group, a 9,9-dimethylfluoren-2,7-diyl group, a 9-chlorofluorene-2,7-diyl group, a 9,9-difluorofluoren-2,7-diyl group, or a 1,4-phenylene group in which any hydrogen is substituted with a halogen atom, a cyano group, a methyl group or trifluoromethyl group; Z 1 and Z 2 each independently represent a single bond, —COO—, —OCO—, —CH 2 CH 2 —, or —C≡C—; X 5 and X 6 each independently represent a single bond or —O—; q independently indicates 1 or 0; o, p and r each independently indicate an integer of from 0 to 20.

16. The liquid-crystal composition as claimed in claim 15 , which contains at least one compound of formula (1) and at least one polymerizable compound selected from the group of compounds of formula (M1) and (M2).

17. The liquid-crystal composition as claimed in claim 15 , which contains at least one compound of formula (1) and at least one polymerizable compound selected from the group of compounds of formula (M3).

18. liquid-crystal composition as claimed in claim 15 , which contains at least one compound of formula (1) and at least one polymerizable compound selected from the group of compounds of formulae (M4) and (M5).

19. The liquid-crystal composition as claimed in claim 15 , which contains at least one compound of formula (1) and at least one polymerizable compound selected from the group of compounds of formula (M1), (M2) and (M3).

20. A polymer obtained by polymerizing the compound of claim 1 .

21. A polymer obtained by polymerizing the composition of claim 11 .

22. An optically-anisotropic shaped article comprising the polymer of claim 20 .

23. A liquid-crystal display device comprising the optically-anisotropic shaped article of claim 22 .

Assignments (4)
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 →
RECORD TO CORRECT THE FIRST INVENTOR'S NAME ON AN ASSIGNMENT PREVIOUSLY RECORDED ON REEL 016407 AND FRAME 0834. Recorded Apr 2, 2008
From: SHUNDO, RYUSHI; ETOU, TOMOHIRO; KIMURA, MASAMI
To: CHISSO CORPORATION; CHISSO PETROCHEMICL CORPORATION
Reel/Frame 020747/0347 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2005
From: SYUNDO, RYUSHI; ETOU, TOMOHIRO; KIMURA, MASAMI
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 016407/0834 →