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首页> 外文期刊>Macromolecular chemistry and physics >Novel fluorinated hybrid polymer by radical polyaddition of bis(alpha-trifluoromethyl-beta,beta-difluorovinyl) terephthalate onto dialkoxydialkylsilanes
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Novel fluorinated hybrid polymer by radical polyaddition of bis(alpha-trifluoromethyl-beta,beta-difluorovinyl) terephthalate onto dialkoxydialkylsilanes

机译:通过将对苯二甲酸双(α-三氟甲基-β,β-二氟乙烯基)对苯二氧基二烷基硅烷自由基加聚来制备新型氟化杂化聚合物

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摘要

To develop the radical polyaddition of bisperfluorisopropenyl esters, the reactions of bis(alpha-trifluromethyl-beta,beta-difluorovinyl) terephthalate [CP2=C(CF3)OCO-C6H4COOC(CF3)=CF2] (BFP) with dialkoxydialkysilane were examined to prepare fluorinated hybrid polymers gearing dialkylsilyl groups in the main chain. Prior to polyaddition, the radical addition reaction of 2-benzoyloxy-pentafluropropene [CF2=C(CF3)OCOC6H5] (BPFP) has been investigated to afford the results that diethoxydimethylsilane (DEOMS) or dimethoxydimethylsilane with BPFP initiated by oxo radical are the best combination for the preparation of polymers. The mechanism of the addition reaction was proposed. Radical polyaddition of BFP with DEOMS initiated by benzoyl peroxide or di-tert-butyl peroxide has yielded polymers of up to molecular weight 1 x 10(6) with rather broad molecular weight distribution. A mechanism for the poly addition reaction is proposed based on the radical addition reaction between BPFP and DEOMS. The step-growth polymerization is initiated by hydrogen abstraction of DEOMS to add a perfluoroisopropenyl group, followed by a 1,7-shift of the radical in the intermediate. The relationship between addition reaction mechanism and polyaddition mechanism was also discussed. [References: 10]
机译:为了开发双全氟异丙烯基酯的自由基加成反应,研究了对苯二甲酸双(α-三氟甲基-β,β-二氟乙烯基)对苯二甲酸酯[CP2 = C(CF3)OCO-C6H4COOC(CF3)= CF2](BFP)与二烷氧基二烷基硅烷的反应在主链上带有二烷基甲硅烷基的氟化杂化聚合物。在加聚之前,已经研究了2-苯甲酰氧基五氟丙烯[CF2 = C(CF3)OCOC6H5](BPFP)的自由基加成反应,结果表明二乙氧基二甲基硅烷(DEOMS)或二甲氧基二甲基硅烷与由氧代自由基引发的BPFP是最佳组合用于制备聚合物。提出了加成反应的机理。过氧化苯甲酰或过氧化二叔丁基引发的BFP与DEOMS的自由基加聚反应产生的聚合物分子量高达1 x 10(6),分子量分布相当宽。基于BPFP与DEOMS之间的自由基加成反应,提出了一种加聚反应的机理。通过DEOMS的氢提取以添加全氟异丙烯基,然后在中间体中将自由基进行1,7位转移来引发逐步增长的聚合反应。还讨论了加成反应机理与加聚机理之间的关系。 [参考:10]

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