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Photo-induced copper-mediated polymerization of methyl acrylate in continuous flow reactors

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Wenn, Benjamin, Conradi, Matthias, Carreiras, Andre Demetrio, Haddleton, David M. and Junkers, Thomas (2014) Photo-induced copper-mediated polymerization of methyl acrylate in continuous flow reactors. Polymer Chemistry, 5 (8). pp. 3053-3060. doi:10.1039/c3py01762a ISSN 1759-9954.

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Official URL: http://dx.doi.org/10.1039/c3py01762a

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Abstract

Photo-induced copper-mediated radical polymerization of methyl acrylate (MA) is carried out in DMSO at 15 °C in a tubular photo-flow reactor as well as in a glass-chip based microreactor. Polymerization reactions proceed rapidly to approximately 90% monomer conversion within 20 minutes of reactor residence time. Control of reactions is high as evidenced by ideal polymerization kinetics, low dispersities of the obtained polymers (in the range of 1.1) and linear evolution of number average molecular weights during polymerization reactions. Poly(MA) with average molecular weights between a few hundred and ∼5000 g mol−1 was obtained under retention of pristine end group fidelity. Besides homopolymers, block copolymers can also be successfully synthesized and poly(methyl acrylate)-b-poly(butyl acrylate) block copolymers with a similar low dispersity are obtained. Reactions proceed under homogeneous reaction conditions. This feature allows the reaction to be carried out in milli- and also in microflow devices. In both cases, equally good control is achieved with only minimal adaptation of the reaction protocol, underpinning the simplicity and fast adaptability of the protocol to different flow reactors.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Divisions: Faculty of Science, Engineering and Medicine > Science > Chemistry
Library of Congress Subject Headings (LCSH): Polymerization, Photochemistry, Methyl acrylate
Journal or Publication Title: Polymer Chemistry
Publisher: Royal Society of Chemistry
ISSN: 1759-9954
Official Date: 21 April 2014
Dates:
DateEvent
21 April 2014Published
24 January 2014Available
23 January 2014Accepted
23 December 2013Submitted
Volume: 5
Number: 8
Number of Pages: 8
Page Range: pp. 3053-3060
DOI: 10.1039/c3py01762a
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Open Access (Creative Commons)
Funder: European Science Foundation (ESF)

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