Synthesis of Photoreactive Block Copolymers Based on 1-Iminopyridinium Ylides
Patrick Theato A B D and Daniel Klinger A CA Institute of Organic Chemistry, University of Mainz, Duesbergweg 10-14, D-55099 Mainz, Germany.
B World Class University (WCU) program of Chemical Convergence for Energy & Environment (C2E2), School of Chemical and Biological Engineering, College of Engineering, Seoul National University (SNU), Seoul, Korea.
C Present address: Max Planck Institute for Polymer Research, Ackermannweg 10, D-55128 Mainz, Germany.
D Corresponding author. Email: theato@uni-mainz.de
Australian Journal of Chemistry 63(8) 1164-1168 https://doi.org/10.1071/CH10079
Submitted: 12 February 2010 Accepted: 6 April 2010 Published: 10 August 2010
Abstract
Two photoreactive pyridinium ylide containing monomers, {[2-(metacryloyloxy)ethoxy]carbonyl}(pyridinium-1-yl)azanide (M1) and pyridinium-1-yl-(4-vinylbenzoyl)azanide (M2), were synthesized. Both monomers were polymerized under controlled radical polymerization conditions, i.e. reversible addition–fragmentation chain transfer polymerization (M1 and M2) and nitroxide-mediated polymerization (M2). Further block copolymers PMMA-b-PM1 and PS-b-PM2 were successfully synthesized and their molecular weight, Mn, and block ratio could be determined by 1H NMR analysis, thereby opening the synthetic possibilities of photoreactive ylides in block copolymer syntheses.
Acknowledgement
Financial support from the University of Mainz is gratefully acknowledged. D.K. acknowledges Dr Georg Scheuing-Stiftung of the University of Mainz for a scholarship. This research was supported by World Class University program through the National Research Foundation of Korea funded by the Ministry of Education, Science and Technology (R31–10013).
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