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首页> 外文期刊>Macromolecules >Manganese-Based Controlled/Living Radical Polymerization of Vinyl Acetate, Methyl Acrylate, and Styrene: Highly Active, Versatile, and Photoresponsive Systems
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Manganese-Based Controlled/Living Radical Polymerization of Vinyl Acetate, Methyl Acrylate, and Styrene: Highly Active, Versatile, and Photoresponsive Systems

机译:乙酸乙烯酯,丙烯酸甲酯和苯乙烯的锰基受控/活性自由基聚合:高活性,多功能和光响应系统

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摘要

The highly active, versatile, and photoresponsive controlled/living radical polymerizations were developed using Mn-2(CO)(10) coupled with an alkyl iodide initiator (R-I) under weak visible light. The photoinduced polymerization of vinyl acetate (VAc) proceeded very fast even at 40 degrees C with a catalytic amount of Mn-2(CO)(10) (0.025 mol% of VAc or 5.0 mol % of R-I) and completed within a few hours to live the polymers with controlled molecular weights up to 10(5). The controlled polymerization was photoresponsive; that is, the polymerization proceeded only during the lighting period while maintaining the controlled molecular weights for the entire period. This system was also effective in controlled radical polymerizations of conjugated monomers such as styrene and methyl acrylate in conjuction with an appropriate alkyl iodide initiator. The contributions of the metal-catalyzed and the degenerative iodine transfer process were also examined by analyzing the model reactions.
机译:在弱可见光下,使用Mn-2(CO)(10)与烷基碘引发剂(R-1)偶联开发了高活性,多功能和光响应受控/活性自由基聚合。乙酸乙烯酯(VAc)的光致聚合反应即使在40摄氏度下也能非常快速地进行,催化量为Mn-2(CO)(10)(0.025 mol%的VAc或5.0 mol%的RI),并在数小时内完成使分子量高达10(5)的聚合物具有活性。受控的聚合反应是光响应的。即,聚合仅在点亮期间进行,而在整个期间内保持控制的分子量。该体系在与合适的烷基碘化物引发剂结合的共轭单体如苯乙烯和丙烯酸甲酯的受控自由基聚合中也是有效的。通过分析模型反应,还研究了金属催化的碘和变性碘转移过程的贡献。

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