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首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Synthesis of Gradient Copolysiloxanes by Simultaneous Copolymerization of Cyclotrisiloxanes and Mechanism for Kinetics Inverse Between Anionic and Cationic Ring-Opening Polymerization
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Synthesis of Gradient Copolysiloxanes by Simultaneous Copolymerization of Cyclotrisiloxanes and Mechanism for Kinetics Inverse Between Anionic and Cationic Ring-Opening Polymerization

机译:环三硅氧烷同时共聚合成梯度共聚硅氧烷的机理及阴离子和阳离子开环聚合反应动力学的逆向机理

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Trifluoropropylmethylsiloxane-phenylmethylsiloxane gradient copolysiloxanes were synthesized by anionic and cationic ring-opening polymerization (ROP) of 1,3,5-tris(trifluoropropylmethyl) cyclotrisiloxane (D-3(F)) and phenylmethylcyclotrisiloxane (D-3(Ph)). The analysis of reactivity ratios revealed that the reactivity of D-3(F) toward anionic ROP was higher than that of D-3(Ph); however, D-3(F) exhibited lower reactivity compared with D-3(Ph) during the cationic ROP. AB and BAB type gradient copolymers were obtained because of a difference in the reactivity of the monomers. The microstructure of copolymers was character-ized by Si-29 NMR spectroscopy, gel permeation chromatography, and differential scanning calorimetry. Furthermore, the mechanism for kinetics inverse of copolymerization was proposed based on the results of the optimized molecular configuration. (C) 2015 Wiley Periodicals, Inc.
机译:通过1,3,5-三(三氟丙基甲基)环三硅氧烷(D-3(F))和苯甲基环三硅氧烷(D-3(Ph))的阴离子和阳离子开环聚合(ROP)合成三氟丙基甲基硅氧烷-苯基甲基硅氧烷梯度共聚硅氧烷。反应比分析表明,D-3(F)对阴离子ROP的反应性高于D-3(Ph)。然而,与阳离子ROP期间的D-3(Ph)相比,D-3(F)的反应性较低。由于单体反应性的差异,获得了AB和BAB型梯度共聚物。共聚物的微结构通过Si-29 NMR光谱,凝胶渗透色谱和差示扫描量热法进行表征。此外,基于最佳分子构型的结果,提出了共聚动力学逆反应的机理。 (C)2015威利期刊公司

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