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Issue 36, 2016
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ADMET and TAD chemistry: a sustainable alliance

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Abstract

A versatile, additive-free post-polymerisation functionalisation method for acyclic diene metathesis (ADMET) derived polymers, utilising 1,2,4-triazoline-3,5-dione (TAD) chemistry, is reported. Several diene monomers have been synthesised starting from 10-undecenoic acid derivatives and subsequently polymerised via ADMET polymerisation reaction. Post-polymerisation functionalisation of the poly-unsaturated macromolecules with several substituted TAD compounds was shown to achieve full conversions within 6 hours. Also, the functionalised polymers could be chemically crosslinked with a bivalent triazolinedione crosslinker. The glass transition temperature of the resulting materials could be tuned by varying the degree of functionalisation, the polymer backbone, the TAD substituent and the crosslinking density.

Graphical abstract: ADMET and TAD chemistry: a sustainable alliance

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Article information


Submitted
01 Jul 2016
Accepted
14 Aug 2016
First published
16 Aug 2016

Polym. Chem., 2016,7, 5655-5663
Article type
Paper

ADMET and TAD chemistry: a sustainable alliance

L. Vlaminck, K. De Bruycker, O. Türünç and F. E. Du Prez, Polym. Chem., 2016, 7, 5655
DOI: 10.1039/C6PY01144F

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