Reactive & Functional Polymers, Vol.101, 70-74, 2016
Synthesis and polymerization of N-(4-ethynylphenyl)maleimide as a novel monomer with two polymerizable and modifiable groups
In this study, a novel monomer molecule, N-(4-ethynylphenyl)maleimide (EPMI) with two polymerizable and modifiable groups (ethynyl and maleimido) was synthesized. Both radical and anionic polymerizations of EPMI at the vinylene group in a maleimide moiety yielded poly[N-(4-ethynylphenyl)maleimide] (PEPMI) with pendent ethynyl groups. The yields of PEPMI were 84.5% and 80.5% from an anionic initiator potassium tert-butoxide at -60 degrees C for 3 h and radical initiator 2,2'-azobisisobutyronitrile at 60 degrees C for 24 h, respectively. EPMI was also polymerized by selective coordination polymerization of the ethynyl moiety with [(nbd)RhCl](2) catalyst to produce poly[(4-maleimido)phenylacetylene] (PMAPA) bearing a poly(phenylacetylene) type main chain with pendent maleimido groups. On the contrary, no polymeric material was obtained with cationic initiators. (C) 2016 Elsevier B.V. All rights reserved.
Keywords:Polymerization of Bifunctional monomer;N-(4-ethynylphenyl)maleimide;Poly[N-(4-substituted phenyl)maleimide];Phenylacetylene derivative