Issue 31, 2014

The 1,3-bis(dicyanomethylidene)indane skeleton as a (photo) initiator in thermal ring opening polymerization at RT and radical or cationic photopolymerization

Abstract

1,3-Bis(dicyanomethylidene)indane is presented as a new initiator for ring opening polymerization of epoxides at RT. This compound behaves as a strong acid (AH) with an associated basic form (A) that does not inhibit the propagation of the cationic polymerization. Remarkably, A is characterized by a strong visible light absorption and can also photosensitize iodonium salt decomposition. A new iodonium salt based on A as a counter-anion is proposed. This latter compound exhibits unusual properties: (i) excellent absorption in the 300–700 nm wavelength range and (ii) a free radical initiating ability for λ > 300 nm. The chemical mechanisms are investigated by ESR, fluorescence and steady state photolysis experiments.

Graphical abstract: The 1,3-bis(dicyanomethylidene)indane skeleton as a (photo) initiator in thermal ring opening polymerization at RT and radical or cationic photopolymerization

Supplementary files

Article information

Article type
Paper
Submitted
08 Jun 2013
Accepted
24 Mar 2014
First published
25 Mar 2014

RSC Adv., 2014,4, 15930-15936

The 1,3-bis(dicyanomethylidene)indane skeleton as a (photo) initiator in thermal ring opening polymerization at RT and radical or cationic photopolymerization

S. Telitel, F. Dumur, T. Kavalli, B. Graff, F. Morlet-Savary, D. Gigmes, J. Fouassier and J. Lalevée, RSC Adv., 2014, 4, 15930 DOI: 10.1039/C3RA42819B

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