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首页> 外文期刊>Journal of Polymer Research >Atom transfer radical polymerization by [RuCl2(PPh3)(2)(amine)] catalysts: Cyclic amines as tuner of reactivity
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Atom transfer radical polymerization by [RuCl2(PPh3)(2)(amine)] catalysts: Cyclic amines as tuner of reactivity

机译:原子通过[RuCl 2(PPH3)(2)(2)(胺)]催化剂转移自由基聚合:环状胺作为反应性的调谐器

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摘要

Atom transfer radical polymerizations (ATRP) of styrene (St) and methyl methacrylate (MMA) mediated by [RuCl2(PPh3)(2)(amine)] complexes, with amine = pyrrolidine (1), piperidine (2), or perhydroazepine (3), were investigated as a function of time, temperature, and concentrations of monomers and 2-bromoisobutyrate as initiator. The plots of ln([M](0)/[M]) vs. time and molecular weights vs. monomer conversion were linear and the dispersity indexes decreased with increasing monomer conversions. The complexes 1, 2, and 3 were able to mediate the polymerizations with acceptable rate and level of control. Differences in the rate and control of polymerization were observed in the order 3 > 2 > 1 for both monomers. The activities were discussed considering the steric hindrance and electronic characteristics of the amines as ancillary ligands in the metal centres, considering studies by cyclic voltammetry and NMR.
机译:苯乙烯(ST)和甲基丙烯酸甲酯(MMA)介导的原子转移自由基聚合(ATRP)(2)(2)(2)(胺)]配合物,胺=吡咯烷(1),哌啶(2),或钙碱( 3)作为时间,温度和单体和2-溴异丁酸酯作为引发剂的时间,温度和浓度的函数进行研究。 LN([m](0)/ [m])的曲线与时间和分子量与单体转化率为线性,并且分散性指数随着单体转化的增加而降低。 配合物1,2和3能够以可接受的速率和对照水平介导聚合。 为两个单体的3> 2> 1,观察到聚合速率和控制的差异。 考虑到循环伏安法和NMR的研究,考虑到金属中心中的辅助配体的空间障碍和电子特性讨论了该活动。

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