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Developing a synthetic approach with thermoregulated phase-transfer catalysis: Facile access to metal-mediated living radical polymerization of methyl methacrylate in aqueous/organic biphasic system

机译:开发具有温度调节相转移催化作用的合成方法:在水/有机双相体系中轻松获得金属介导的甲基丙烯酸甲酯的金属活性自由基聚合

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摘要

A novel strategy via thermoregulated phase-transfer catalysis (TRPTC) to separating catalyst in aqueous/organic biphasic system has been successfully established in a copper-mediated activators generated by electron transfer for atom transfer radical polymerization (AGET ATRP) of methyl methacrylate (MMA), using a thermoresponsive PEG-supported dipyridyl ligand (PSDL) as the ligand and an alkyl pseudohalogen 2-cyanoprop-2-yl 1-dithionaphthalate (CPDN) as the initiator. The catalyst complex can transfer into the organic phase from initial catalyst aqueous solution at the reaction temperature (90 C) to catalyze the homogeneous polymerization of MMA and then retransfer into the aqueous solution from the organic phase to separate the catalyst from the polymerization solution once cooled to room temperature (25 C) while remaining well-controlled product (PMMA) in organic layer. In addition, the polymerization can be conducted in the presence of a limited amount of air, which not only does not sacrifice the controllability over polymerization but also can recycle the catalyst just by a simple change of the temperatures effectively.
机译:已成功建立了一种通过热调节相转移催化(TRPTC)分离水/有机双相系统中催化剂的新策略,该方法通过电子转移生成的铜介导活化剂进行甲基丙烯酸甲酯(MMA)的原子转移自由基聚合(AGET ATRP)。 ,使用具有热响应性的PEG负载的二吡啶基配体(PSDL)作为配体,并使用烷基假卤素2-氰基丙-2-基1-二硫代萘二甲酸(CPDN)作为引发剂。催化剂配合物可以在反应温度(90℃)下从初始催化剂水溶液转移到有机相中,以催化MMA的均相聚合,然后一旦冷却就从有机相转移到水溶液中以将催化剂从聚合溶液中分离出来到室温(25 C),同时在有机层中保留良好控制的产品(PMMA)。另外,聚合可以在有限量的空气存在下进行,这不仅不牺牲聚合的可控性,而且仅通过简单地有效地改变温度就可以使催化剂再循环。

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