Volume 214, Issue 13 p. 1473-1483
Full Paper

Radical Polymerization of MMA Co-initiated by 2-Phenyloxazoline

Ingmar Polenz,

Corresponding Author

Harvard University, School of Engineering and Applied Sciences, 9 Oxford Street, Cambridge, MA 02138, USA

Ingmar Polenz, Harvard University, School of Engineering and Applied Sciences, 9 Oxford Street, Cambridge, MA 02138, USA

Stefan Spange, Institut für Chemie, Polymerchemie, Technische Universität Chemnitz, Straße der Nationen 62, 09111 Chemnitz, Germany.

Search for more papers by this author
Friedrich Georg Schmidt,

Evonik Industries AG, Coatings and Additives, Paul-Baumann-Straße 1, 45772 Marl, Germany

Search for more papers by this author
Joachim Friedrich,

Institut für Chemie, Theoretische Chemie, Technische Universität Chemnitz, Straße der Nationen 62, 09111 Chemnitz, Germany

Search for more papers by this author
Ivan Tchernook,

Institut für Chemie, Theoretische Chemie, Technische Universität Chemnitz, Straße der Nationen 62, 09111 Chemnitz, Germany

Search for more papers by this author
Stefan Spange,

Corresponding Author

Institut für Chemie, Polymerchemie, Technische Universität Chemnitz, Straße der Nationen 62, 09111 Chemnitz, Germany

Ingmar Polenz, Harvard University, School of Engineering and Applied Sciences, 9 Oxford Street, Cambridge, MA 02138, USA

Stefan Spange, Institut für Chemie, Polymerchemie, Technische Universität Chemnitz, Straße der Nationen 62, 09111 Chemnitz, Germany.

Search for more papers by this author
First published: 27 May 2013
Citations: 10

Abstract

The subject of this work is the study of a new type of radical polymerization that occurs at elevated temperatures (80–100 °C) in mixtures of acrylates or (meth)acrylates and imine baes (IBA polymerization). The radical character of this polymerization is proven by the determination of copolymerization ratios and the reaction kinetics. On the basis of these facts and the hypothesis that the vinyl monomer acts as a co-initiator, calculations reveal the concentration of the initiating species to be very low (Keq < 10−6). Furthermore, the choice of the reaction medium plays a crucial role on reaction kinetics and the average molecular weight of the resulting polymer. In combination with computational methodologies on the initiation, the multistep nature of this reaction is indicated.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.