4.7 Article

Bifunctional co-initiators: A new strategy for the design of efficient systems in radical photopolymerization reactions under air

Journal

EUROPEAN POLYMER JOURNAL
Volume 48, Issue 5, Pages 956-962

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eurpolymj.2012.01.022

Keywords

Radical chemistry; Silyl radical; Photopolymerization; Oxygen inhibition

Funding

  1. French Agency for Research ANR [ANR-BLAN-0802, ANR SILICIUM]

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Bifunctional co-initiators containing amine and silane groups (silylamines) are proposed for radical photopolymerization in experimental conditions (e.g. low light intensity, low viscosity thin samples, UV and visible light exposure) where a strong deleterious oxygen effect occurs. In the presence of benzophenone, isopropylthioxanthone, camphorquinone, 2,6-diphenyl-4-(4'-dimethylaminophenyl) thiopyrylium tetrafluoroborate, chloro-HABI and cleavable photoinitiators, these compounds show a high reactivity under air, even better than that observed for a reference amine as a hydrogen donor. The associated mechanisms are investigated by laser flash photolysis (LFP) and Kinetic ESR. (C) 2012 Elsevier Ltd. All rights reserved.

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