IP Library Granted Patent US 11,124,524
Granted Patent B2
US 11,124,524 · App. 16/374,571 · Granted Sep 21, 2021

Diarylethene compounds and uses thereof

Inventors: Neil Robin Branda (North Vancouver, CA); Jeremy Graham Finden (North Vancouver, CA); Simon James Gauthier (Vancouver, CA); Ali Hayek (Burnaby, CA); Kyle Andrew Hope-Ross (Vancouver, CA); James Daniel Senior (Surrey, CA); Andreea Spantulescu (New Westminster, CA); Serguei Sviridov (Burnaby, CA)
Assignee: Solutia Canada Inc.
C07D495/04C07D277/22C07D307/79C07D333/12C07D333/18C07D333/22C07D333/38C07D409/14C07D493/04C07D493/14C07D493/22C07D495/14C07D513/04C07D513/14C07D519/00C07F7/0814C07F7/1804C09K9/02G02B1/04G02B5/20G02B5/223G02B5/23C09K2211/1007C09K2211/1088C09K2211/1092
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Quick Facts
Patent No.
US 11,124,524
App. No.
16/374,571
Granted
Sep 21, 2021
Kind
B2
Abstract

A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R 1 is independently selected from the group consisting of H, or halo; each R 2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R 2 together form —CH═CH— and form part of a polymer backbone; each R 3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R 4 is aryl; and each R 5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.

Claims (55)

1. A compound according to Formula XA/XB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B:

wherein:

Z is independently O or S;

each R 1 is independently H or halo;

each R 2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl and aryl; or both R 2 together form —CH═CH—;

R 3 is

each R 4 is independently aryl,

 with the proviso that R 4 is not aryl or

 when R 3 is

X═N, O, or S;

R 5 is H or alkyl;

each R 6a , R 6b , R 6c , each R 7a , R 7b , R 7c , each R 8a , R 8b , R 8c , R 8d , R 8e , each R 9a , R 9b , R 9c , R 9d , R 9e is independently selected from the group consisting of: H, Cl, Br, F, —CF 3 , —CN, —NO 2 , methyl, ethyl, propyl, iso-propyl, butyl, sec-butyl, iso-butyl, tert-butyl, saturated or unsaturated alkyl that is linear or branched with 5 to 12 carbons, —Si(R 11 ) 3 , thiophene, substituted thiophene, benzyl, substituted benzyl, —CH═CH 2 , —OCH 3 , —COH, —OH, —CO 2 H, —COCH 3 , —C(CH 3 ) 2 OH, —Si(CH 3 ) 3 , —CH 2 CH 2 OCH 3 , —CH 2 CH 2 OH, —N(CH 3 ) 2 , —CO 2 CH 3 , —OCH 2 OCH 3 , —SO 2 CH 3 , —OCH 2 C(CH 3 ) 3 , —OCH 2 CH(CH 3 ) 2 , —OC(CH 3 ) 3 , —OCH═CH 2 , —O(CH 2 ) 4 CN, —O(CH 2 ) 4 OH, —O(CH 2 ) 3 OH, —C(CH 3 ) 2 OH, —O(CH 2 ) 2 OCH 3 ,

n and m are independently any integer from 0 to 20;

R 6a and R 6b , or R 6b and R 6c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring;

R 7a and R 7b , or R 7b and R 7c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring;

R 11 is independently selected from the group consisting of R and —O—R, wherein:

R is linear or branched, non-aromatic monocyclic or polycyclic, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any one of 1 to 20 carbons; or

R is a heteroalkyl group comprising one or more of O, S, N or Si; or

R is a linear or branched, saturated or unsaturated, alkyl group comprising a carbon backbone comprising any one of 1 to 12 carbons; or

R is a substituted or unsubstituted methyl, ethyl, propyl, iso-propyl, butyl, sec-butyl, iso-butyl, tert-butyl, pentyl or hexyl group; and

each of R 10a , R 10b , R 10c , and R 10d , is individually selected from a group consisting of an electron donating group, an electron withdrawing group, —OCH 3 , —CN, —OH, H,

or R 10b and R 10c are each O and joined by —CH 2 — to form a 5-membered ring.

2. The compound according to claim 1 wherein R 3 is

a first R 4 group residing on the same ring moiety as R 3 is

and a second R 4 group residing on a different ring moiety as R 3 is

and

wherein R 6a and R 6b or R 6b and R 6c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring, and

wherein R 7a and R 7b or R 7b and R 7c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring.

3. The compound according to claim 2 wherein each of R 10b and R 10c is an electron donating group.

4. The compound according to claim 3 wherein the electron donating group is —OR 14 where R 14 is:

a linear or branched, non-aromatic monocyclic or polycyclic, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any one of 1 to 20 carbons;

a heteroalkyl group comprising one or more of O, S, N or Si;

a linear or branched, saturated or unsaturated alkyl group comprising a carbon backbone comprising any one of 1 to 12 carbons; or

a substituted or unsubstituted methyl, ethyl, propyl, iso-propyl, butyl, sec-butyl, iso-butyl, tert-butyl, pentyl or hexyl group.

5. The compound according to claim 4 wherein R 14 is the heteroalkyl group comprising one or more of O, S, N or Si.

6. The compound according to claim 1 wherein R 3 is

and each R 4 is independently

and

wherein R 6a and R 6b or R 6b and R 6c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring, and

wherein R 7a and R 7b or R 7b and R 7c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring.

7. The compound according to claim 1 wherein R 3 is

and each R 4 is independently

and

wherein R 6a and R 6b or R 6b and R 6c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring.

8. The compound according to claim 1 wherein R 3 is

a first R 4 group residing on the same ring moiety as R 3 is

and a second R 4 group residing on a different ring moiety as R 3 is

and

wherein R 6a and R 6b or R 6b and R 6c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring, and

wherein R 7a and R 7b or R 7b and R 7c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring.

9. The compound according to claim 1 wherein R 3 is

and each R 4 is independently

and

wherein R 7a and R 7b or R 7b and R 7c are each a) —CH═CH— and joined to form a 6-membered ring, b) —C(R 12 ) 2 —C(R 12 ) 2 — and joined to form a 6-membered ring where each R 12 is independently H or alkyl that is a linear or branched, saturated or unsaturated, substituted or unsubstituted alkyl group comprising a carbon backbone comprising any of 1 to 12 carbons, or c) —O—CH 2 — and joined to form a 6-membered ring.

10. The compound according to claim 1 wherein R 1 and R 2 are F.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2021
From: BRANDA, NEIL ROBIN; FINDEN, JEREMY GRAHAM; GAUTHIER, SIMON JAMES; SVIRIDOV, SERGUEI; HAYEK, ALI; SENIOR, JAMES DANIEL; HOPE-ROSS, KYLE ANDREW; SPANTULESCU, ANDREEA
To: SWITCH MATERIALS, INC.
Reel/Frame 056675/0975 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2021
From: BRANDA, NEIL ROBIN; FINDEN, JEREMY GRAHAM; GAUTHIER, SIMON JAMES; HAYEK, ALI; HOPE-ROSS, KYLE ANDREW; SENIOR, JAMES DANIEL; SVIRIDOV, SERGUEI
To: SWITCH MATERIALS, INC.
Reel/Frame 056676/0003 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 13, 2021
From: SWITCH MATERIALS INC.
To: SOLUTIA CANADA INC.
Reel/Frame 054902/0819 →
Continuity (7)
Continuation 16045186 · Jul 25, 2018
Continuation 14947230 · Nov 20, 2015
Continuation 14348344 · Mar 28, 2014
Continuation In Part PCTCA2012000910 · Sep 28, 2012
Provisional Application 61541841 · Sep 30, 2011
Provisional Application 61675460 · Jul 25, 2012
Related Publication 20190256526A1 · Aug 22, 2019