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Stereospecific Radical Polymerization of #alpha#-(Alkoxymethyl)acrylates Controlled by a Catalytic Amount of Zinc Halides

机译:催化量卤化锌控制的#α#-(烷氧基甲基)丙烯酸酯的立体定向自由基聚合

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摘要

The stereospecific radical polymerization of #alpha#-(alkoxymethyl)acrylates-benzyl #alpha#-(methoxymethyl)acrylate, benzyl #alpha#-(ethoxymethyl)acrylate, and ethyl #alpha#-(ethoxymethyl)acrylate-in hte presence of a catalytic amount of zinc halides (ZnCl_2 and ZnBr_2) was attained, and the obtained polymers had very different tacticities, rich in syndiotacticity (up to r = 0.71), from that prepared in the absence of a zinc salt (atactic). In contrast, no change was observed in the stereoregularity of the polymethacrylates radically obtained in the presence of ZnBr_2 as an additive. The coordination of zinc salts to polar #alpha#-substituents on the #omega#-end of the propagating polymer and the monomer must play an important part in this system.
机译:#α#-(烷氧基甲基)丙烯酸酯-苄基#α#-(甲氧基甲基)丙烯酸酯,苄基#α#-(乙氧基甲基)丙烯酸酯和乙基#α#-(乙氧基甲基)丙烯酸酯的立体定向自由基聚合达到了催化量的卤化锌(ZnCl_2和ZnBr_2),所得聚合物的立构规整度与不存在锌盐时(无规立构)的立构规整度大(高达r = 0.71)。相反,在存在ZnBr_2作为添加剂的情况下自由基获得的聚甲基丙烯酸酯的立构规整度没有观察到变化。锌盐与正在繁殖的聚合物和单体的#omega#末端上的极性#α#取代基的配位必须在该系统中发挥重要作用。

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