IP Library Granted Patent US 7,682,522
Granted Patent B2
US 7,682,522 · App. 12/266,744 · Granted Mar 23, 2010

Polymerizable menthol derivative

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Quick Facts
Patent No.
US 7,682,522
App. No.
12/266,744
Granted
Mar 23, 2010
Kind
B2
Abstract

The invention includes compounds represented by Formula (1): wherein R represents hydrogen or methyl; A represents alkylene having from 1 to 12 carbon atoms, wherein in the alkylene, arbitrary —CH 2 — may be replaced by —O—, —S—, —CH═CH—, —CO—, —COO— or —OCO—; X and Y each independently represent an aromatic ring or a cyclohexane ring, wherein in the rings, arbitrary hydrogen may be replaced by alkyl having from 1 to 3 carbon atoms; Z independently represents a single bond, —O—, —S—, —COO—, —OCO—, —CON(R 1 )— or —N(R 1 )CO—, wherein R 1 represents hydrogen or methyl; and m represents an integer of from 0 to 3.

Claims (25)

1. A compound represented by formula (1):

wherein

R represents hydrogen or methyl;

A represents alkylene having from 1 to 12 carbon atoms, wherein in the alkylene, arbitrary —CH 2 — may be replaced by —O—, —S—, —CH═CH—, —CO—, —COO— or —OCO—;

X and Y each independently represent an aromatic ring or a cyclohexane ring, wherein in the rings, arbitrary hydrogen may be replaced by alkyl having from 1 to 3 carbon atoms;

Z independently represents a single bond, —O—, —S—, —COO—, —OCO—, —CON(R 1 )— or —N(R 1 )CO—, wherein R 1 represents hydrogen or methyl; and

m represents an integer of from 0 to 3.

2. The compound according to claim 1 , wherein in formula (1), —(X—Z) m —Y— is a structure represented by formula (2-1) or (2-2):

3. The compound according to claim 1 , wherein in formula (1), —(X—Z) m —Y— is a structure represented by one of formulae (3-1) to (3-7):

4. The compound according to claim 1 , wherein in formula (1), —(X—Z) m —Y— is a structure represented by one of formulae (4-1) to (4-4):

5. The compound according to claim 1 , wherein in formula (1), A represents —CH 2 CH 2 CH 2 CH 2 — or —CH 2 CH 2 —.

6. The compound according to claim 1 , wherein in formula (1), A represents —CH 2 CH 2 OCH 2 CH 2 — or —CH 2 CH 2 —O—CH 2 CH 2 —O—CH 2 CH 2 —.

7. A liquid crystal composition comprising the compound according to claim 1 and a liquid crystal compound.

8. A liquid crystal composition comprising the compound according to claim 2 and a liquid crystal compound.

9. A liquid crystal composition comprising the compound according to claim 3 and a liquid crystal compound.

10. A liquid crystal composition comprising the compound according to claim 4 and a liquid crystal compound.

11. A liquid crystal composition comprising the compound according to claim 5 and a liquid crystal compound.

12. A liquid crystal composition comprising the compound according to claim 6 and a liquid crystal compound.

13. The liquid crystal composition according to claim 7 , wherein the liquid crystal composition comprises at least one polymerizable liquid crystal compound as the liquid crystal compound.

14. A polymer comprising the liquid crystal composition according to claim 13 having been polymerized.

15. The polymer according to claim 14 , wherein the polymer exhibits a cholesteric liquid crystal phase.

16. A method for using the liquid crystal composition according to claim 7 as a liquid crystal pigment, a paint, a spray ink, a printing ink, a cosmetic product, an anticounterfeit printed matter, an ornamental article and an optical film.

17. A method for using the liquid crystal composition according to claim 13 as a liquid crystal pigment, a paint, a spray ink, a printing ink, a cosmetic product, an anticounterfeit printed matter, an ornamental article and an optical film.

18. A method for using the polymer according to claim 14 as a liquid crystal pigment, a paint, a spray ink, a printing ink, a cosmetic product, an anticounterfeit printed matter, an ornamental article and an optical film.

19. A method for using the polymer according to claim 15 as a liquid crystal pigment, a paint, a spray ink, a printing ink, a cosmetic product, an anticounterfeit printed matter, an ornamental article and an optical film.

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 Jan 7, 2009
From: TANABE, MAYUMI
To: CHISSO CORPORATION; CHISSO PETROCHEMICAL CORPORATION
Reel/Frame 022083/0607 →