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Synthesis of substituted polymethylenes from acenaphthylene by radical polymerization and copolymerization

机译:以苊为原料的自由基聚合和共聚合成取代聚亚甲基

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AbstractRadical polymerization of acenaphthylene (Ace) as a 1,2‐disubstituted ethylene was investigated. It was found that the polymerization rate (Rp) was expressed as follows:Rp=kAce1.0AIBN0.68, and that the overall activation energy was 113 kJ/mol for polymerization with 2,2'‐azobisisobutyronitrile (AIBN) in benzene at 50–70°C. Poly(Ace) obtained was characterized by NMR spectroscopy and GPC. Some substituted copolymethylenes were also prepared by radical copolymerization of Ace with other 1,2‐disubstituted ethylenes, that is, maleic anhydride, diisopropyl fumarate, andN‐cyclohexylmaleimide. The monomer reactivity ratios were determined from comonomer–copolymer compos
机译:摘要研究了1,2-二取代乙烯的苊(Ace)自由基聚合反应。结果表明,在50–70°C下,与2,2'-偶氮二异丁腈(AIBN)在苯中聚合时,聚合速率(Rp)表示为:Rp=k[Ace]1.0[AIBN]0.68,总活化能为113 kJ/mol。 通过核磁共振波谱和GPC对Poly(Ace)进行了表征。将Ace与其他1,2-二取代乙烯(即马来酸酐、富马酸二异丙酯和N-环己基马来酰亚胺)自由基共聚制备了一些取代的共聚亚甲基。单体反应性比由共聚单体-共聚物组合测定

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