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Synthesis and polymerization of N-(4-ethynylphenyl)maleimide as a novel monomer with two polymerizable and modifiable groups

机译:具有两个可聚合和可修饰基团的新型单体N-(4-乙炔基苯基)马来酰亚胺的合成与聚合

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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.
机译:在这项研究中,合成了一种新型的单体分子,具有两个可聚合和可修饰的基团(乙炔基和马来酰亚胺基)的N-(4-乙炔基苯基)马来酰亚胺(EPMI)。 EPMI在马来酰亚胺部分的亚乙烯基上的自由基和阴离子聚合均产生具有侧基乙炔基的聚[N-(4-乙炔基苯基)马来酰亚胺](PEPMI)。阴离子引发剂叔丁醇钾在-60摄氏度下3 h和自由基引发剂2,2'-偶氮二异丁腈在60摄氏度下24 h的PEPMI收率分别为84.5%和80.5%。还通过乙炔基部分与[(nbd)RhCl](2)催化剂的选择性配位聚合反应来聚合EPMI,以生产带有带有悬垂马来酰亚胺基团的聚(苯乙炔)型主链的聚[(4-马来酰亚胺基)苯基乙炔](PMAPA)。 。相反,没有用阳离子引发剂获得聚合物材料。 (C)2016 Elsevier B.V.保留所有权利。

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