Issue 2, 2014

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

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

Supplementary files

Article information

Article type
Communication
Submitted
22 Jūl. 2013
Accepted
14 Aug. 2013
First published
13 Sept. 2013

Mater. Horiz., 2014,1, 237-240

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements