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Issue 2, 2014
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Catalyst-free room-temperature self-healing elastomers based on aromatic disulfide metathesis

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Abstract

Aromatic disulfide metathesis has been reported as one of the very few dynamic covalent chemistries undergone at room-temperature. Here, bis(4-aminophenyl) disulfide is effectively used as a dynamic crosslinker for the design of self-healing poly(urea–urethane) elastomers, which show quantitative healing efficiency at room-temperature, without the need for any catalyst or external intervention.

Graphical abstract: Catalyst-free room-temperature self-healing elastomers based on aromatic disulfide metathesis

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Article information


Submitted
22 Jul 2013
Accepted
14 Aug 2013
First published
13 Sep 2013

Mater. Horiz., 2014,1, 237-240
Article type
Communication

Catalyst-free room-temperature self-healing elastomers based on aromatic disulfide metathesis

A. Rekondo, R. Martin, A. Ruiz de Luzuriaga, G. Cabañero, H. J. Grande and I. Odriozola, Mater. Horiz., 2014, 1, 237
DOI: 10.1039/C3MH00061C

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