Issue 5, 2013

Reversible click chemistry at the service of macromolecular materials. Part 4: Diels–Alder non-linear polycondensations involving polyfunctional furan and maleimide monomers

Abstract

The polymerisation of furan monomers and the exploitation of some of the chemical peculiarities of the furan heterocycle have generated a wide diversity of macromolecular materials based on renewable resources. In particular, the application of the DA cycloaddition to the macromolecular chemistry opened new ways to synthesize materials with unique properties, such as self-mendability and network recyclability. In this study, non-linear polycondensations between di- and tri-functional furan (An) and maleimide (Bm) monomers by means of the DA reaction are presented. The use of complementary monomers bearing more than two functionalities led to highly crosslinked structures under appropriate stoichiometric conditions, and thus, can be applied in the preparation of “mendable” materials.

Graphical abstract: Reversible click chemistry at the service of macromolecular materials. Part 4: Diels–Alder non-linear polycondensations involving polyfunctional furan and maleimide monomers

Article information

Article type
Paper
Submitted
28 Sep 2012
Accepted
18 Oct 2012
First published
18 Oct 2012

Polym. Chem., 2013,4, 1364-1371

Reversible click chemistry at the service of macromolecular materials. Part 4: Diels–Alder non-linear polycondensations involving polyfunctional furan and maleimide monomers

A. Gandini, A. Silvestre and D. Coelho, Polym. Chem., 2013, 4, 1364 DOI: 10.1039/C2PY20805A

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