Catalyst for living radical polymerization and polymerization method
US-9546226-B2 · Jan 17, 2017 · US
US9908979B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9908979-B2 |
| Application number | US-201314395108-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 15, 2013 |
| Priority date | Apr 18, 2012 |
| Publication date | Mar 6, 2018 |
| Grant date | Mar 6, 2018 |
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The present invention provides a method for producing polythiophene star copolymer capable of being self-doped by an external stimulus, which includes the steps of: forming a polythiophene macroinitiator made by introducing a living radical polymerizable functional group into an end of polythiophene or a derivative thereof; forming through living radical polymerization a polymer macroinitiator for providing by an external stimulus at least a dopant selected from the group consisting of sulfonic acid radical, carboxylic acid radical and phosphoric acid radical; and polymerizing the polythiophene macroinitiator added with the polymer macroinitiator and at least one kind of divinyl monomer to produce the polythiophene star copolymer. The polythiophene star copolymer capable of being self-doped by an external stimulus according to the present invention is a self-doped material to stably increase conductivity, and can be used as a material for a conductive film.
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The invention claimed is: 1. A polythiophene star copolymer capable of being self-doped by an external stimulus, comprising: a microgel core comprising a homopolymer of a divinyl monomer or a copolymer of two or more divinyl monomers; polythiophene or derivative thereof bonded to the core; and a hetero arm chain comprising a polymer including at least one dopant selected from a group consisting of a sulfonic acid group, a carboxylic acid group and a phosphoric acid group, wherein the polymer including at least one dopant is at least one selected from a group consisting of poly(neopentyl styrene sulfonate), poly(t-butyldimethyl(4-vinylphenyl) phosphonate), poly(diethyl(4-vinylphenyl) phosphonate), poly(di(t-butyl)(4-vinylphenyl) phosphonate) and poly(t-butyl acrylate), and wherein the polythiophene or the derivative thereof is represented by a chemical formula selected from a group consisting of Chemical Formula 1, Chemical Formula 2 and Chemical Formula 3: wherein n is an integer from 0 to 12 and m is an integer from 1 to 90 wherein m is an integer from 1 to 90, R′ is —C n H 2n+1 and n is an integer from 1 to 12 wherein m is an integer from 1 to 90, R 1 and R 2 are selected from the R in Chemical Formula 2, and R 1 and R 2 may be identical or different. 2. The polythiophene star copolymer according to claim 1 , wherein the divinyl monomer is at least one selected from a group consisting of a diacrylate compound, an ethylene glycol dimethacrylate compound, a diacrylamide compound, a divinylphenyl compound, a divinylnaphthalene compound and a divinyltoluene compound. 3. A method for producing a polythiophene star copolymer according to claim 1 comprising: forming a polythiophene macroinitiator made by introducing a living radical polymerizable functional group into an end of polythiophene or a derivative thereof; forming through living radical polymerization a polymer macroinitiator for providing by an external stimulus at least one dopant selected from a group consisting of a sulfonic acid group, a carboxylic acid group and a phosphoric acid group; and polymerizing the polythiophene macroinitiator added with the polymer macroinitiator and at least one kind of divinyl monomer to produce the polythiophene star copolymer, wherein the polythiophene star copolymer comprises: a microgel core comprising a homopolymer of a divinyl monomer or a copolymer of two or more divinyl monomers; polythiophene or a derivative thereof bonded to the core; and a hetero arm chain comprising a polymer providing by an external stimulus at least one dopant selected from a group consisting of a sulfonic acid group, a carboxylic acid group and a phosphoric acid group. 4. The method for producing a polythiophene star copolymer according to claim 3 , wherein the polymer macroinitiator is obtained by introducing at least one selected from a group consisting of an atom transfer radical polymerization (ATRP) macroinitiator, a nitroxide-mediated polymerization (NMP) macroinitiator and a reversible addition-fragmentation chain transfer (RAFT) macroinitiator into at least one selected from a group consisting of poly(neopentyl styrene sulfonate), poly(t-butyldimethyl(4-vinylphenyl) phosphonate), poly(diethyl(4-vinylphenyl) phosphonate), poly(di(t-butyl)(4-vinylphenyl) phosphonate) and poly(t-butyl acrylate). 5. The method for producing a polythiophene star copolymer according to claim 1 , wherein the divinyl monomer is at least one selected from a group consisting of a diacrylate compound, an ethylene glycol dimethacrylate compound, a diacrylamide compound, a divinylphenyl compound, a divinylnaphthalene compound, and a divinyltoluene compound. 6. A method for producing a conductive film using a polythiophene star copolymer according to claim 1 comprising: providing a substrate; coating the substrate with the polythiophene star copolymer; and post-treating the substrate with at least one selected from heat, light and an acidic chemical. 7. The method for producing a conductive thin film according to claim 6 , wherein the substrate is surface-treated by at least one method selected from a group consisting of piranha solution treatment, acid treatment, base treatment, plasma treatment, atmospheric pressure plasma treatment, ozone treatment, UV treatment and polymer or single molecule coating. 8. The method for producing a conductive thin film according to claim 6 , wherein the heat treatment as the post-treating is conducted at 150-250° C. 9. A composition for coating a substrate, comprising the polythiophene star copolymer according to claim 1 .
dendritic · CPC title
Characterised by the use of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain (C08J2307/00 - C08J2357/00, C08J2361/00 take precedence); Derivatives of such polymers · CPC title
Charge transport · CPC title
containing sulfonyl or sulfonate-groups · CPC title
Of polythioether · CPC title
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