Electrochromic composition

Patent metadata

Field	Value
Publication number	US-9785030-B2
Application number	US-201415022775-A
Country	US
Kind code	B2
Filing date	Sep 16, 2014
Priority date	Sep 17, 2013
Publication date	Oct 10, 2017
Grant date	Oct 10, 2017

Abstract

The present invention relates to an electrochromic composition comprising at least one reducing compound and at least two oxidizing compounds, said at least two oxidizing compounds having similar oxydo-reduction potentials. More specifically, said at least two oxidizing compounds are selected from viologen derivatives. Said composition can be used as a variable transmittance medium for the manufacture of an optical article, such as an ophthalmic lens.

First claim

The invention claimed is:

1. An electrochromic composition comprising:
at least one reducing compound; and
at least two electrochromic oxidizing compounds,

wherein said electrochromic oxidizing compounds have similar oxydo-reduction potentials, and are selected from viologen derivatives of formulae (I) and (II):

wherein:
R 1 and R 2 are each independently selected from optionally substituted phenyl groups;
R 3 , R 4 , R 5 and R 6 are each independently selected from H, alkyl, alkoxy, alkylthio, haloalkyl, haloalkoxy, haloalkythio, polyakylenoxy, alkoxycarbonyl, aryl, substituted aryl, heteroaryl and substituted heteroaryl, wherein the alkyl group may be substituted by one or more substituents independently selected from alkoxy, cycloalkyl, aryl, substituted aryl, heteroaryl and substituted heteroaryl;
n, p, q and r are each independently an integer from 0 to 4, wherein when n, p, q or r is two or more, each of the R 3 , each of the R 4 , each of the R 5 or each of the R 6 may be identical or different;
A and B are respectively selected from nitrogen and —N + (R 7a )—, and from nitrogen and —N + (R 7b )—, wherein R 7a and R 7b are independently selected from:
alkyl which may be substituted by one or more groups independently selected from halogen, alkoxy, cycloalkyl, vinyl, allyl, aryl, substituted aryl, heteroaryl and substituted heteroaryl;
aryl and heteroaryl which may be both substituted by one or more groups independently selected from:
halogen, cyano, nitro, alkyl, haloalkyl, arylalkyl, cycloalkyl, cycloalkylalkyl and heterocycloalkylalkyl, alkenyl, alkynyl, allyl, vinyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, —N(aryl) 2 , —N(aryl)CO(aryl), —CO-aryl and —CO-substituted aryl;
—OR 8 , —S(O)R 8 , —S(O 2 )R 8 , —S(O 2 )NR 8 R 9 , —NR 8 R 9 , —NR 8 COR 9 , —NR 8 CO(aryl), —NR 8 aryl, —CH 2 OR 8 , —CH 2 SR 8 , —CH 2 R 8 , —CO—R 8 and —CO 2 R 8 wherein R 8 and R 9 are independently selected from H, alkyl, haloalkyl, arylalkyl, cycloalkyl, cycloalkylalkyl and heterocycloalkylalkyl;
—S(O 2 )NR 10 R 11 and —NR 10 R 11 , wherein R 10 and R 11 form together with the nitrogen atom to which they are linked a saturated 5 to 7 membered heterocycloalkyl which may comprise in addition to the nitrogen atom one further heteroatom selected from oxygen, nitrogen and sulphur, and which may be optionally substituted by one or two groups independently selected from halogen, —R 8 , —OR 8 , and —NR 8 R 9 , wherein R 8 and R 9 are as defined above;
—V—W—R 12 wherein:
V is selected from oxygen, —N(R 8 )—, sulphur, —S(O)— and —S(O 2 )— wherein R 8 is as defined above;
W is alkylene, which may be substituted by one or more groups independently selected from halogen and alkoxy; and
R 12 is selected from —OR 8 , —NR 8 (alkyl) and —SR 8 wherein R 8 is as defined above; and
—OC(O)—R 13 wherein R 13 is selected from alkyl, haloalkyl, alkenyl, —W—R 12 , and aryl group which may be substituted by 1 to 4 groups selected from halogen, —R 8 , —OR 8 , —SR 8 , —NR 8 R 9 , —NR 10 R 11 , —CO—R 8 , C(O)OR 8 , wherein R 8 , R 9 , R 10 , R 11 , R 12 and W are as defined above;

Z is selected from:
alkylene;
cycloalkylene; and
a bivalent groups of formula —R 14 —Y—R 15 —, wherein:
R 14 and R 15 are each independently selected from single bond, alkylene and cycloalkylene, and
Y is selected from arylene, cycloalkylene, heteroarylene, arylene-arylene or arylene-CR′R″-arylene wherein R′ and R″ form together with the carbon to which they are linked a carbocyclic group;

wherein said alkylene, cycloalkylene, arylene, heteroarylene and carbocyclic groups may be substituted by one or more substituents selected from halogen, alkyl, alkoxy, alkylthio, hydroxyalkyl, acyloxy, cycloalkyl, aryl, substituted aryl, aryloxy heteroaryl and substituted heteroaryl;

m is 2 if A and B are nitrogen, 3 if one of A and B is nitrogen and the other is not nitrogen, and 4 if both A and B are not nitrogen;
X − is a counterion;
at least one of the viologen derivatives is selected from compounds of formula (I); and
at least one of the viologen derivative is selected from compounds of formula (III) or formula (IV):

wherein Z, and X − are as defined in formula (II), and R 16 and R 17 are independently selected from substituted phenyl groups of formula (VI):

wherein R a and R b are independently selected from H, halogen, cyano, nitro, hydroxyl, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, acyl, aroyl, alkoxycarbonyl, cycloalkyl, allyl, aryl, benzyl, and heteroaryl provided that at least one of R a and R b is not H

wherein R 4 , R 5 , Z, A, B, m and X − are as defined in formula (II) and at least one of R 4 and R 5 is not H.

2. The electrochromic composition according to claim 1 , wherein the oxydo-reduction potentials of the electrochromic oxidizing compounds differ from each other from less than 0.2 V.

3. The electrochromic composition according to claim 2 , wherein the oxydo-reduction potentials of the electrochromic oxidizing compounds differ from each other from less than 0.15 V.

4. The electrochromic composition according to claim 3 , wherein the oxydo-reduction potentials of the electrochromic oxidizing compounds differ from each other from less than 0.1 V.

5. The electrochromic composition according to claim 4 , wherein the oxydo-reduction potentials of the electrochromic oxidizing compounds differ from each other from less than 0.05 V.

6. The electrochromic composition according to claim 1 , wherein Z is selected from C 1 -C 12 alkylene, aryl substituted C 1 -C 12 alkylene, phenylene, naphthylene, (C 1 -C 4 alkylene)-phenylene-(C 1 -C 4 alkylene), (C 1 -C 4 alkylene)-naphthylene-(C 1 -C 4 alkylene), quinoxaline-2,3-diyl, (C 1 -C 4 alkylene)-quinoxaline-2,3-diyl-(C 1 -C 4 alkylene), phenylene-phenylene, (C 1 -C 4 alkylene)-phenylene-phenylene-(C 1 -C 4 alkylene) and phenylene-fluorenylene-phenylene.

7. The electrochromic composition according to claim 6 , wherein Z is selected from —CH 2 —, —(CH 2 ) 2 —, —(CH 2 ) 3 —, —(CH 2 ) 4 —, —(CH 2 ) 5 —, —CH 2 —CH(CH 3 )—CH 2 —, —CH 2 —CH(CH 2 Phenyl)-CH 2 —, —(CH 2 ) 2 —CH(CH 3 )—CH 2 —, —(CH 2 ) 3 —CH(CH 3 )—CH 2 —, —(CH 2 ) 2 —CH(CH 3 )—(CH 2 ) 2 —,

8. The electrochromic composition according to claim 1 , wherein R 3 , R 4 , R 5 and R 6 are each independently selected from C 1 -C 4 alkyl, C 1 -C 4 alkoxycarbonyl, alkanoyl, aroyl, aryl and heteroaryl, and wherein the aryl and heteroaryl may be substituted by one or more substituents selected from C 1 -C 4 alkyl and C 1 -C 4 haloalkyl.

9. The electrochromic composition according to claim 1 , wherein the counterion X − is selected from halide, tetrafluoroborate, tetraphenylborate, hexafluorophosphate, nitrate, methanesulfonate, trifluoromethane sulfonate, toluene sulfonate, hexachloroantimonate, bis(trifluoromethanesulfonyl)imide, perchlorate, acetate and sulfate.

10. The electrochromic composition according to claim 1 , wherein said viologen derivatives are selected from compounds I-1 to I-50, III-7 to III-19 and IV-1 and IV-14:

Assignees

• Essilor Int

Inventors

• Biver Claudine
• Archambeau Samuel
• Berit-Debat Fabien

Classifications

• G02C7/101

  having an electro-optical light valve (electro-optical elements per se G02F) · CPC title

• C09K9/02

  Organic tenebrescent materials · CPC title

• G02C7/10

  Filters, e.g. for facilitating adaptation of the eyes to the dark; Sunglasses · CPC title

• G02F1/1521 Primary

  Physics · mapped topic

• G02F1/15

  based on an electrochromic effect · CPC title