IP Library Granted Patent US 7,416,682
Granted Patent B2
US 7,416,682 · App. 10/519,148 · Granted Aug 26, 2008

Photochromic liquid crystals

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Quick Facts
Patent No.
US 7,416,682
App. No.
10/519,148
Granted
Aug 26, 2008
Kind
B2
Abstract

The invention relates to novel photochromic liquid crystal materials which may be used in various electro-optic devices including liquid crystal devices. The materials can be converted into another form on irradiation by light which may make it feasible for them to be addressed by light in electro-optic devices. The materials are based on 5-membered heterocycles.

Claims (37)

1. A material given by Formula I and Ib:

Wherein the

groups are chosen respectively from the following:

are together chosen from:

* indicates the point of attachment to Formula I or Formula Ib;

the phenyl groups in

may independently of each other be replaced by pyridine and pyrimidine groups;

wherein X is selected from S, O, NH, Se, CH 2 , P;

wherein J is selected from CF 2 , CH 2 , CFH, NR 9 wherein R9 is selected from H, C1-40 branched or straight chain alkyl wherein one or more of the CH 2 groups may be replaced by O, CH and the terminal CH 3 group may be replaced by a CH 2 group or an SH, OH, COOH, CHO, O 2 CCHCH 2 or O 2 CC(CH 3 )CH 2 group;

wherein a and d are independently selected from CH 3 , CF 3 , CH 2 CH 3 , OCH 3 , OCH 2 CH 3 or Formula II;

b, c, e and f are independently selected from H, Formula II or C1-40 branched or straight chain alkyl wherein one or more of the CH 2 groups may be replaced by O, CFH, CF 2 , CH and the terminal CH 3 group may be replaced by a CH 2 group or an SH, OH, CF 3 , COOH, CHO, O 2 CCHCH 2 or O 2 CC(CH 3 )CH 2 group

wherein Formula II is given by:

wherein Y is selected from O, —CO 2 —, O 2 C, S, CH 2 , or a single bond;

Q is selected from (CH 2 )n, n is 1-20 or (CH 2 )m-[Si(L2)-O]q-Si(L2)-(CH 2 )p- where m is 2-20, p is 2-20, q is 1-12 and the L groups are independently of each other selected from CH 3 , CF 3 , H;

Z is O or CO 2 or O 2 C or CH 2 or a single bond;

is a mesogenic group;

T is 1 or 2 or 3;

when T is 2 then Q may also be selected from (CH 2 )gN((CH 2 )r) 2 , (CH 2 )gSi(CH 3 )((CH 2 )r) 2 , (CH 2 )gP((CH 2 )r) 2 , (CH 2 )gGe(CH 3 )((CH 2 )r) 2 , wherein the values of g and r are independently selected from 1-20;

when T is 3 then Q may also be selected from (CH 2 )g′Si((CH 2 )r′) 3 , and (CH 2 )g′Ge((CH 2 )r′) 3 ;

wherein the values of g′ and r′ are independently selected from 1-20;

provided that at least one of a, b, c, d, e, f are selected from Formula II.

2. A material according to claim 1 wherein the mesogenic group is given by Formula III:

A, B, B′ D are selected from the following rings:

the above rings may be substituted with one or more of the following substituents in at least one of the available substitution positions: F, Cl, Br, CH 3 , CN, OR, R and NCS where R is given by C 1-16 branched or straight chain alkyl; B′ may also be selected from single bond;

Z 5 is selected from CN, F, Cl, NO 2 , R, OR, CO 2 R, CF 3 , OOCR, NCS, SCN, where R=straight chain or branched chain alkyl and may include from 1-16 carbon atoms and including where one or more non-adjacent CH 2 groups may be substituted by CH(CN), CH(CF 3 ), CH(Cl), CH(CH 3 ) in chiral or non-chiral form and one or more non-adjacent CH 2 groups may be substituted by CH such that there is a double bond present and the terminal CH 3 group may be replaced by a CH 2 group;

provided that the total number of rings present is not greater than 4;

W 1 and W 2 and W 3 are independently selected from COO, OCO, single bond, CH 2 CH 2 , CH 2 O, OCH 2 , O, S, CH═CH, C═C, OCO(CH 2 ) x , COO(CH 2 ) x wherein x is 1-4.

3. A material according to claim 1 wherein the mesogenic group or at least a part of the mesogenic group is given by the cholesteryl group or a derivative of the cholesteryl group.

4. A material according to claim 1 wherein the core of the mesogenic group is chosen from the following:

wherein in each of the mesogenic groups, one or two or three of the phenyl rings may be, independently of each other, replaced by cyclohexyl, pyrimidine or pyridine and the cyclohexyl groups and phenyl groups may independently of each other be substituted in one or two or three positions with F, the CO 2 group may also be replaced with O 2 C or C═C.

5. A liquid crystal mixture comprising at least one compound of claim 1 .

6. An electro-optic device comprising at least one compound of claim 1 .

7. An electro-optic device comprising a mixture as defined in claim 5 .

8. A device according to claim 6 wherein the electro-optic device is a liquid crystal device.

9. A device according to claim 7 wherein the electro-optic device is a liquid crystal device.

10. A device according to claim 6 which is multiplex addressed or is addressed by light.

11. A device according to claim 7 which is multiplex addressed or is addressed by light.

Assignments (4)
CHANGE OF NAME Recorded Apr 3, 2014
From: CHIMEI INNOLUX CORPORATION
To: INNOLUX CORPORATION
Reel/Frame 032604/0487 →
MERGER Recorded May 12, 2010
From: CHI MEI OPTOELECTRONICS CORP.
To: CHIMEI INNOLUX CORPORATION
Reel/Frame 024369/0316 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 31, 2007
From: QINETIQ LIMITED
To: CHI MEI OPTOELECTRONICS CORP.
Reel/Frame 020299/0484 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 27, 2004
From: FRIGOLI, MICHAEL; MEHL, GEORG H.
To: QINETIQ LIMITED
Reel/Frame 016818/0596 →