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Vinyl acetate living radical polymerization mediated by cobalt porphyrins: kinetic-mechanistic studies

机译:醋酸乙烯酯自由基聚合由钴卟啉:kinetic-mechanistic研究

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摘要

Radical polymerization of vinyl acetate (VAc) in the presence of cobalt(II) tetramesitylporphyrin, Co~(II)(TMP), as a mediator was performed in a series of solvent environments. Cobalt porphyrin was observed to mediate an effective living radical polymerization reaction of vinyl acetate in bulk as shown by the linear increase in molecular weight with conversion, relatively narrow molecular weight distributions (M_w/M_n = 1.24-1.34), and molecular weights close to the theoretical value up to moderately high monomer conversions (~70%). The levels of deviation for the observed PVAc molecular weights from the .theoretieal values varied with the choice of solvent medium, which suggests that the control of vinyl acetate radical polymerization was affected by chain transfer to the solvent. Non-coordinating solvents influence the polymerization rate primarily by different propagation rate constants (K_p). Pyridine coordination with dormant organo-cobalt(III) increases the dissociation constant and changes the dominant polymerization process from degenerative transfer to reversible termination.
机译:自由基聚合的醋酸乙烯(VAc)钴(II) tetramesitylporphyrin的存在,公司~ (II) (TMP),在执行作为调停者系列溶剂的环境。观察到调解是一个有效的生活醋酸乙烯酯的自由基聚合反应散装如图所示的线性增加相对分子量与转换窄分子量分布(M_w / M_n =1.24 - -1.34),和分子量接近理论价值比较高的单体转换(~ 70%)。观察到的PVAc的分子量.theoretieal值随的选择溶剂介质,这表明控制醋酸乙烯酯的自由基聚合通过链转移溶剂的影响。Non-coordinating溶剂的影响聚合速率主要是由不同传播速率常数(K_p)。配合休眠organo-cobalt (3)增加了离解常数和变化占主导地位的聚合过程退行性转移到可逆终止。

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