On the Mechanism of Radical Polymerization of Methyl Methacrylate with Dithiobenzoic Acid as Mediator
Duc Hung Nguyen A and Philipp Vana A BA Institut für Physikalische Chemie, Georg-August-Universität Göttingen, 37077 Göttingen, Germany.
B Corresponding author. Email: pvana@uni-goettingen.de
Australian Journal of Chemistry 59(8) 549-559 https://doi.org/10.1071/CH06158
Submitted: 11 May 2006 Accepted: 5 July 2006 Published: 8 September 2006
Abstract
Dithiobenzoic acid (DTBA) induces controlled polymerization behaviour in methyl methacrylate polymerization at 60°C, accompanied by a pronounced induction period of several hours. DTBA is partially transformed during this induction period into a dithioester with a tertiary ester group moiety, which constitutes an efficient reversible addition–fragmentation chain transfer (RAFT) agent. The transformation reaction is proposed to proceed via a hydrogen abstraction from DTBA by radicals and subsequent termination of the formed phenylcarbonothioylsulfanyl radical with propagating radicals. The proposed reaction scheme was implemented into a computer model, by which the rate coefficient of the hydrogen abstraction from DTBA and of the reinitiation of the intermediate phenylcarbonothioylsulfanyl radical was estimated. The model is in agreement with all of the species observable by electrospray ionization mass spectrometry, with the extent of the experimental induction periods, and with the absolute concentrations of dithioesters that act as efficient RAFT agents during the polymerization. A protocol that uses a cocktail of initiators is introduced, by which the induction period in DTBA-mediated polymerization is effectively eliminated.
Acknowledgments
Financial support by the Deutsche Forschungsgemeinschaft within the frame of the Graduate School 782 ‘Spectroscopy and Dynamics of Molecular Coils and Aggregates’ is gratefully acknowledged. We thank Professor M. Buback for valuable discussions and Dr H. Frauendorf for help with the mass spectrometry.
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