Macromolecules, 38 (12), 5025 -5034, 2005. 10.1021/ma0474170 S0024-9297(04)07417-0
Web Release Date: May 18, 2005

Copyright © 2005 American Chemical Society

Investigation of the Living Cationic Ring-Opening Polymerization of 2-Methyl-, 2-Ethyl-, 2-Nonyl-, and 2-Phenyl-2-oxazoline in a Single-Mode Microwave Reactor

Frank Wiesbrock, Richard Hoogenboom, Mark A. M. Leenen, Michael A. R. Meier, and Ulrich S. Schubert*

Laboratory of Macromolecular Chemistry and Nanoscience, Eindhoven University of Technology (TU/e) and Dutch Polymer Institute (DPI), Den Dolech 2, 5600 MB Eindhoven, The Netherlands

Received December 15, 2004

Revised Manuscript Received April 17, 2005

Abstract:

The living cationic ring-opening polymerizations of 2-methyl-, 2-ethyl-, 2-nonyl-, and 2-phenyl-2-oxazoline were performed in acetonitrile at high temperatures of up to 200 C in a single-mode microwave reactor. Upon enhancing the reaction rates by factors of up to 400 in the range from 80 to 200 C, the first-order kinetics of the monomer consumption and the livingness of the polymerization were maintained. As a consequence of the fast, direct, and noncontact heating by the microwave irradiation, the polymerizations could be carried out in highly concentrated solutions or even from bulk conditions, yielding well-defined polymers (PDI < 1.20). Under the conditions applied in this study, a maximum number of 300 monomers (100 in the case of 2-methyl- and 2-nonyl-2-oxazoline) could be incorporated into the polymer chains under the premise that the average molecular weight distributions remained narrow (PDI < 1.20).


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