Adhesive composition comprising a polyurethane and a cationic dopant

US12031065B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12031065-B2
Application numberUS-202218070843-A
CountryUS
Kind codeB2
Filing dateNov 29, 2022
Priority dateOct 7, 2019
Publication dateJul 9, 2024
Grant dateJul 9, 2024

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

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An adhesive composition comprising a polyurethane and a cationic polymeric dopant or a polymerizable cationic dopant may be used to form one or more adhesive layers of electro-optic assemblies. They enable improved electro-optic performance of the corresponding; electro-optic devices even at low temperatures.

First claim

Opening claim text (preview).

The invention claimed is: 1. An electro-optic assembly comprising, in order, an electrically-conductive light-transmissive layer, an electro-optic material layer in electrical contact with the electrically-conductive light-transmissive layer. an adhesive laver, and a backplane substrate, the electro-optic material layer comprising an electrophoretic medium including a plurality of charged particles in a fluid, the adhesive layer comprising a polyurethane and a homopolymer, the homopolymer being formed during a curing process via polymerization of a polymerizable cationic dopant, the polymerizable cationic dopant being represented by Formula II, wherein R9 is hydrogen or a methyl group; R10 is an alkyl group having from 1 to 10 carbon atoms; q is from 1 to 5; and Y n− is a counter ion, the counterion being selected from the group consisting of 1,1,2,2-tetrafluoroethane sulfonic acid, hexafluorosilicic acid, tris(perfluoroalkyl)trifluorophosphate, 2,2,2-trifluoromethylsulfonyl-N-cyanoamide, heptadecafluorooctanesulfonic acid, 1,1,1-trifluoro-N-((trifluoromethyl)sulfonyl)methanesulfonamide, bis(perfluoroethylsulfonyl)amide, bis[(trifluoromethyl)sulfonyl]imide, bis(fluorosulfonyl)imide, fluorotrifluoromethylsulfonyl imide, (fluorosulfonyl)(pentafluoroethanesulfonyl)imide, (trifluoromethylsulfonyl)(pentafluoroethanesulfonyl)imide. 2. The electro-optic assembly according to claim 1 , wherein the counterion is a multi-atom anion comprising at least three fluorine atoms. 3. The electro-optic assembly according to claim 1 , wherein the number average molecular weight of the cationic part of the polymerizable cationic dopant without including the multi-atom anionic counter ion is from about 183 Daltons to about 415 Daltons. 4. The electro-optic assembly according to claim 1 , wherein the number average molecular weight of the cationic part of the polymerizable cationic dopant without including the multi-atom anionic counter ion is from about 190 Daltons to about 300 Daltons. 5. The electro-optic assembly according to claim 1 , wherein the polyurethane is selected from the group consisting of a polyether polyurethanes and a polyester polyurethane. 6. The electro-optic assembly according to claim 1 , wherein the polyurethane is formed by a reaction of a diisocyanate with a diol or a polyol. 7. The electro-optic assembly according to claim 6 , wherein the diol is an oligomer with two or more reactive alcohol groups. 8. The electro-optic assembly according to claim 6 , wherein the polyol is polyethylene glycol, polypropylene glycol (PPO), or polytetramethylene glycol. 9. The electro-optic assembly according to claim 6 , wherein the diisocyanate is 4,4-methylenebis(cyclohexylisocyanate) (H12MDI), α,α,α,α-tetramethylxylene diisocyanate, 3,5,5-trimethyl-1-isocyanato-3-isocyanatomethylcyclohexane isophorone diisocyanate and derivatives thereof, tetramethylene diisocyanate, hexamethylene diisocyanate (HDI) and derivatives thereof, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, isophorone diisocyanate, m-isopropenyl-α,α-dimethylbenzyl isocyanate, benzene 1,3-bis(1-iscyanato-1-methylethyl, 1-5 naphthalene diisocyanate, phenylene diisocyanate, trans-cyclohexane-1,4-diisocyanate, bitolylene diisocyanate, 4,4′-diphenylmethane diisocyanate, 4,4′-diphenyl dimethyl methane diisocyanate, di- and tetraalkyl diphenyl methane diisocyanate, 4,4′-dibenzyl diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, the isomers of tolylene diisocyanate, 1-methyl-2,4-diisocyanatocyclohexane, 1,6-diisocyanato-2,2,4-trimethyl hexane, 1,6-diisocyanato-2,4,4-trimethyl hexane, 1-isocyanatomethyl-3-isocyanatomethyl-3-isocyanato-1,5,5-trimethyl cyclohexane, chlorinated and brominated diisocyanates, phosphorus-containing diisocyanates, 4,4′-diisocyanatophenyl perfluoroethane, tetramethoxy butane-1,4-diisocyanate, butane-1,4-diisocyanate, hexane-1,6-diisocyanate, dicyclohexyl methane diisocyanate, cyclohexane-1,4-diisocyanate, ethylene diisocyanate, phthalic acid-bis-isocyanatoethyl ester, also polyisocyanates containing reactive halogen atoms, such as 1-chloromethylphenyl-2,4-diisocyanate, 1-bromomethylphenyl-2,6-dusocyanate, 3,3-bis-chloromethylether-4,4′-diphenyl diisocyanate or 4,4-methylenebis(cyclohexylisocyanate). 10. The electro-optic assembly according to claim 1 , wherein the polymerizable cationic dopant is represented by Formula IIA,

Assignees

Inventors

Classifications

  • Interconnections, e.g. wiring lines or terminals · CPC title

  • from polyesters · CPC title

  • Dummy elements, i.e. elements having non-functional features · CPC title

  • Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00 · CPC title

  • Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers · CPC title

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What does patent US12031065B2 cover?
An adhesive composition comprising a polyurethane and a cationic polymeric dopant or a polymerizable cationic dopant may be used to form one or more adhesive layers of electro-optic assemblies. They enable improved electro-optic performance of the corresponding; electro-optic devices even at low temperatures.
Who is the assignee on this patent?
E Ink Corp
What technology area does this patent fall under?
Primary CPC classification C08G18/0866. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 09 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).