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In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP

A completely metal-free and environmentally friendly strategy is demonstrated for the preparation of graft copolymers by combining photoinduced Atom Transfer Radical Polymerization (ATRP) and Ring Opening Polymerization (ROP). Polymerizations are simultaneously realized in a one-pot manner. For this...

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Autor principal: Yilmaz, Gorkem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473307/
https://www.ncbi.nlm.nih.gov/pubmed/33029081
http://dx.doi.org/10.1080/15685551.2020.1808414
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author Yilmaz, Gorkem
author_facet Yilmaz, Gorkem
author_sort Yilmaz, Gorkem
collection PubMed
description A completely metal-free and environmentally friendly strategy is demonstrated for the preparation of graft copolymers by combining photoinduced Atom Transfer Radical Polymerization (ATRP) and Ring Opening Polymerization (ROP). Polymerizations are simultaneously realized in a one-pot manner. For this purpose, bare vinyl monomers, vinyl monomers with hydroxyl functional groups, and lactone monomers were simultaneously polymerized under visible light using specific catalysts. While vinyl monomers construct the main chain, the lactone monomers were polymerized from the hydroxyl functions present at the side chain. Spectral and chromatographic analyses prove that the utilized strategy is successful in the preparation of graft copolymers controlled molecular weights and narrow distributions.
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spelling pubmed-74733072020-10-06 In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP Yilmaz, Gorkem Des Monomers Polym Articles A completely metal-free and environmentally friendly strategy is demonstrated for the preparation of graft copolymers by combining photoinduced Atom Transfer Radical Polymerization (ATRP) and Ring Opening Polymerization (ROP). Polymerizations are simultaneously realized in a one-pot manner. For this purpose, bare vinyl monomers, vinyl monomers with hydroxyl functional groups, and lactone monomers were simultaneously polymerized under visible light using specific catalysts. While vinyl monomers construct the main chain, the lactone monomers were polymerized from the hydroxyl functions present at the side chain. Spectral and chromatographic analyses prove that the utilized strategy is successful in the preparation of graft copolymers controlled molecular weights and narrow distributions. Taylor & Francis 2020-08-18 /pmc/articles/PMC7473307/ /pubmed/33029081 http://dx.doi.org/10.1080/15685551.2020.1808414 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Yilmaz, Gorkem
In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP
title In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP
title_full In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP
title_fullStr In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP
title_full_unstemmed In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP
title_short In-situ syntheses of graft copolymers by metal-free strategies: combination of photoATRP and ROP
title_sort in-situ syntheses of graft copolymers by metal-free strategies: combination of photoatrp and rop
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473307/
https://www.ncbi.nlm.nih.gov/pubmed/33029081
http://dx.doi.org/10.1080/15685551.2020.1808414
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