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Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks

Nowadays, finely controlling the mechanical properties of polymeric materials is possible by incorporating supramolecular motifs into their architecture. In this context, the synthesis of a side-chain terpyridine-functionalized poly(2-(dimethylamino)ethyl methacrylate) is reported via reversible add...

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Autores principales: Brassinne, Jérémy, Jochum, Florian D., Fustin, Charles-André, Gohy, Jean-François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307286/
https://www.ncbi.nlm.nih.gov/pubmed/25569082
http://dx.doi.org/10.3390/ijms16010990
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author Brassinne, Jérémy
Jochum, Florian D.
Fustin, Charles-André
Gohy, Jean-François
author_facet Brassinne, Jérémy
Jochum, Florian D.
Fustin, Charles-André
Gohy, Jean-François
author_sort Brassinne, Jérémy
collection PubMed
description Nowadays, finely controlling the mechanical properties of polymeric materials is possible by incorporating supramolecular motifs into their architecture. In this context, the synthesis of a side-chain terpyridine-functionalized poly(2-(dimethylamino)ethyl methacrylate) is reported via reversible addition-fragmentation chain transfer polymerization. By addition of transition metal ions, concentrated aqueous solutions of this polymer turn into metallo-supramolecular hydrogels whose dynamic mechanical properties are investigated by rotational rheometry. Hence, the possibility for the material to relax mechanical constrains via dissociation of transient cross-links is brought into light. In addition, the complex phenomena occurring under large oscillatory shear are interpreted in the context of transient networks.
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spelling pubmed-43072862015-02-02 Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks Brassinne, Jérémy Jochum, Florian D. Fustin, Charles-André Gohy, Jean-François Int J Mol Sci Article Nowadays, finely controlling the mechanical properties of polymeric materials is possible by incorporating supramolecular motifs into their architecture. In this context, the synthesis of a side-chain terpyridine-functionalized poly(2-(dimethylamino)ethyl methacrylate) is reported via reversible addition-fragmentation chain transfer polymerization. By addition of transition metal ions, concentrated aqueous solutions of this polymer turn into metallo-supramolecular hydrogels whose dynamic mechanical properties are investigated by rotational rheometry. Hence, the possibility for the material to relax mechanical constrains via dissociation of transient cross-links is brought into light. In addition, the complex phenomena occurring under large oscillatory shear are interpreted in the context of transient networks. MDPI 2015-01-05 /pmc/articles/PMC4307286/ /pubmed/25569082 http://dx.doi.org/10.3390/ijms16010990 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Brassinne, Jérémy
Jochum, Florian D.
Fustin, Charles-André
Gohy, Jean-François
Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks
title Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks
title_full Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks
title_fullStr Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks
title_full_unstemmed Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks
title_short Revealing the Supramolecular Nature of Side-Chain Terpyridine-Functionalized Polymer Networks
title_sort revealing the supramolecular nature of side-chain terpyridine-functionalized polymer networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307286/
https://www.ncbi.nlm.nih.gov/pubmed/25569082
http://dx.doi.org/10.3390/ijms16010990
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