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, A; Coelho, D; Silvestre, AJD
nationality International
journal EUROPEAN POLYMER JOURNAL
author keywords Click chemistry; Diels-Alder reaction; Furan-maleimide adducts; Reversible polymerization; Kinetics
keywords ANHYDRIDE
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 H-1 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.
publisher PERGAMON-ELSEVIER SCIENCE LTD
issn 0014-3057
year published 2008
volume 44
issue 12
beginning page 4029
ending page 4036
digital object identifier (doi) 10.1016/j.eurpolymj.2008.09.026
web of science category Polymer Science
subject category Polymer Science
unique article identifier WOS:000262068400015
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journal impact factor 3.862
5 year journal impact factor 4.166
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