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 Reversible click chemistry at the service of macromolecular materials. Part 1: Kinetics of the Diels-Alder reaction applied to furan-maleimide model compounds and linear polymerizations
Please use this identifier to cite or link to this item http://hdl.handle.net/10773/5230

title: Reversible click chemistry at the service of macromolecular materials. Part 1: Kinetics of the Diels-Alder reaction applied to furan-maleimide model compounds and linear polymerizations
authors: Gandini, Alessandro
Coelho, Dora
Silvestre, Armando J.D.
keywords: Click chemistry
Diels–Alder reaction
Furan–maleimide adducts
Reversible polymerization
Kinetics
issue date: 2008
publisher: Elsevier
abstract: The model Diels-Alder reaction of furfuryl acetate with N-methylmaleimide and the linear polymerization of the corresponding difunctional monomers were followed by both UV and (1)H NMR spectroscopy. The results obtained from this study provided clear-cut indications about the most appropriate conditions to be applied in the preparation of novel macromolecular materials based in part oil renewable resources and possessing thermoreversible, mendable and recycling features, among other properties. (C) 2008 Elsevier Ltd. All rights reserved.
URI: http://hdl.handle.net/10773/5230
ISSN: 0014-3057
publisher version/DOI: http://dx.doi.org/10.1016/j.eurpolymj.2008.09.026
source: European Polymer Journal
appears in collectionsDQ - Artigos

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