IP Library Granted Patent US 7,238,831
Granted Patent B2
US 7,238,831 · App. 10/056,121 · Granted Jul 3, 2007

Mesogens

Assignee: Southwest Research Institute
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Quick Facts
Patent No.
US 7,238,831
App. No.
10/056,121
Granted
Jul 3, 2007
Kind
B2
Abstract

Novel platform mesogens, intermediates, and polymerizable mesogens made therefrom.

Claims (42)

1. Mesogens having the following formula:

wherein

X is a polymerizable group,

Y consists essentially of an amino group;

R 2 is selected from the group consisting of hydrogen and a methyl group.

2. The mesogens of claim 1 wherein said polymerizable groups have polymerizable unsaturated carbon-carbon bond.

3. The mesogens of claim 1 wherein said polymerizable groups are selected from the group consisting of acryloyloxy alkoxy groups and methacryloyloxy alkoxy groups having alkyl moiety with from 2 to 12 carbon atoms.

4. The mesogens of claim 3 wherein said alkyl moiety consists essentially of from 2 to 12 carbons atoms and CH 2 groups optionally are substituted by groups selected from the group consisting of oxygen, sulfur, and ester groups; provided that from 2 to 12 carbon atoms separate said oxygen from said ester groups.

5. The mesogens of claim 4 , wherein said alkyl moiety consists essentially of a total of from 2 to 9 carbon atoms.

6. The mesogens of claim 4 , wherein said alkyl moiety consists essentially of a total of from 2 to 6 carbon atoms.

7. The mesogens of claim 1 wherein X is cinnamoyloxy group.

8. Mesogens having the following formula

wherein

X is a polymerizable group selected from the group consisting of acryloyloxy alkoxy groups and methacryloyloxy alkoxy groups having alkyl moiety with from 2 to 12 carbon atoms;

Y consists essentially of an amino group;

R 2 is selected from the group consisting of alkyl groups having from about 1 to 6 carbon atoms and aryl groups; and

R 1 and R 3 are selected from hydrogen and a methyl group.

9. The mesogens of claim 8 , wherein said alkyl moiety consists essentially of 2 to 12 carbons atoms and CH 2 groups optionally are substituted by groups selected from the group consisting of oxygen, sulfur, and ester groups; provided that from 2 to 12 carbon atons separate said oxygen from said ester groups.

10. The mesogens of claim 9 wherein said alkyl moiety consists essentially of a total of from 2 to 9 carbon atoms.

11. The mesogens of claim 9 wherein said alkyl moiety consists essentially of a total of from 2 to 6 carbon atoms.

12. The mesogens of claim 8 wherein X is cinnamoyloxy group.

13. Mesogens having the following formula:

wherein X and Y independently are selected from the group consisting of spacer groups, polymerizable groups, and combinations thereof, wherein one or more members selected from the group consisting of X and Y have the following structure:

wherein Z is selected from the group consisting of spacer groups, terminal functionalities, polymerizable groups, and combinations thereof, said spacer groups being selected from the group consisting of H-(CH 2 ) n -O- groups, Cl(CH 2 ) n -O- groups, Br(CH 2 ) n -O- groups, wherein n is from about 2 to about 12 wherein the CH 2 groups independently can be substituted by oxygen, sulfur, or an ester group; provided that from 2 to 12 carbons separate said oxygen or said ester group;

R 2 is selected from the group consisting of alkyl groups having from 1 to 6 carbon atoms and aryl groups; and

R 1 to and R 3 is selected from the group consisting of hydrogen and a methyl group.

14. The mesogens of claim 13 wherein n is from about 2 to 9.

15. The mesogens of claim 13 wherein n is from about 2 to 6.

16. The mesogens of claim 13 wherein said polymerizable groups have an alkyl moiety having a polymerizable unsaturated carbon-carbon bond.

17. The mesogens of claim 13 wherein said polymerizable groups have an alkyl moiety having a polymerizable unsaturated carbon-carbon bond.

18. The mesogens of claim 16 wherein said alkyl moiety has from 2 to 9 atoms.

19. The mesogens of claim 16 wherein said alkyl moiety has from 2 to 6 atoms.

20. The mesogens of claim 13 wherein R 2 is selected from the group consisting of methyl groups, t-butyl groups, isopropyl groups, secondary butyl groups, and phenyl groups.

21. The mesogens of claim 13 wherein R 2 is selected from the group consisting of methyl groups, t-butyl groups, isopropyl groups, secondary butyl groups, and phenyl groups.

22. The mesogens of claim 16 wherein R 2 is selected from the group consisting of methyl groups, t-butyl groups, isopropyl groups, secondary butyl groups, and phenyl groups.

23. The mesogens of claim 17 wherein R 2 is selected from the group consisting of methyl groups, t-butyl groups, isopropyl groups, secondary butyl groups, and phenyl groups.

24. The mesogens of claim 19 wherein R 2 is selected from the group consisting of methyl groups, secondary butyl groups, and phenyl groups.

25. The mesogens of claim 23 wherein R 1 and R 3 are selected from the group consisting of hydrogen and a methyl group.

26. The mesogens of claim 24 wherein R 1 and R 3 are selected from the group consisting of hydrogen and a methyl group.

27. The mesogens of claim 13 wherein one or more members selected from the group consisting of X and Y is a cinnamoyloxy group.

28. The mesogens of claim 20 wherein one or moreo members selected from the group consisting of X and Y is a cinnamoyloxy group.

29. The mesogens of claim 24 wherein one or more members selected from the group consisting of X and Y is a cinnamoyloxy group.

Assignments (3)
CONFIRMATORY LICENSE Recorded Jan 6, 2011
From: SOUTHWEST RESEARCH INSTITUTE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025590/0843 →
CONFIRMATORY LICENSE Recorded Dec 15, 2008
From: SOUTHWEST RESEARCH INSTITUTE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021977/0433 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2002
From: WELLINGHOFF, STEPHEN T.; HANSON, DOUGLAS P.
To: SOUTHWEST RESEARCH INSTITUTE
Reel/Frame 013006/0346 →
Continuity (4)
Provisional Application 6026338700 · Jan 23, 2001
Provisional Application 6026339200 · Jan 23, 2001
Provisional Application 6026338800 · Jan 23, 2001
Related Publication 20020177727A1 · Nov 28, 2002