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Diffusion-Regulated Phase-Transfer Catalysis for Atom Transfer Radical Polymerization of Methyl Methacrylate in an Aqueous/Organic Biphasic System

机译:扩散调控相转移催化在水/有机双相体系中甲基丙烯酸甲酯的原子转移自由基聚合

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摘要

A concept based on diffusion-regulated phase-transfer catalysis (DRPTC) in an aqueous-organic biphasic system with copper-mediated initiators for continuous activator regeneration is successfully developed for atom transfer radical polymerization (ICAR ATRP) (termed DRPTC-based ICAR ATRP here), using methyl methacrylate (MMA) as a model monomer, ethyl -bromophenylacetate (EBrPA) as an initiator, and tris(2-pyridylmethyl)amine (TPMA) as a ligand. In this system, the monomer and initiating species in toluene (organic phase) and the catalyst complexes in water (aqueous phase) are simply mixed under stirring at room temperature. The trace catalyst complexes transfer into the organic phase via diffusion to trigger ICAR ATRP of MMA with ppm level catalyst content once the system is heated to the polymerization temperature (75 degrees C). It is found that well-defined PMMA with controlled molecular weights and narrow molecular weight distributions can be obtained easily. Furthermore, the polymerization can be conducted in the presence of limited amounts of air without using tedious degassed procedures. After cooling to room temperature, the upper organic phase is decanted and the lower aqueous phase is reused for another 10 recycling turnovers with ultra low loss of catalyst and ligand loading. At the same time, all the recycled catalyst complexes retain nearly perfect catalytic activity and controllability, indicating a facile and economical strategy for catalyst removal and recycling.
机译:一种基于水-有机双相体系中具有扩散调节的相转移催化(DRPTC)的概念,该体系具有铜介导的引发剂,用于连续活化剂的再生,已成功用于原子转移自由基聚合(ICAR ATRP)(此处称为基于DRPTC的ICAR ATRP) ),使用甲基丙烯酸甲酯(MMA)作为模型单体,使用溴溴乙酸乙酯(EBrPA)作为引发剂,使用三(2-吡啶基甲基)胺(TPMA)作为配体。在该系统中,简单地在室温下搅拌下将甲苯(有机相)中的单体和引发剂与水(水相)中的催化剂配合物混合。一旦将体系加热到聚合温度(75摄氏度),痕量催化剂络合物就会通过扩散转移到有机相中,从而触发MMA的ICAR ATRP,催化剂含量为ppm级。发现可以容易地获得具有受控分子量和窄分子量分布的良好定义的PMMA。此外,可以在有限量的空气存在下进行聚合,而无需使用乏味的脱气程序。冷却至室温后,将上层有机相倒出,将下层水相重新用于另外10次循环转换,催化剂和配体的负载量极低。同时,所有回收的催化剂配合物都保留了近乎完美的催化活性和可控性,这表明催化剂的去除和回收既简便又经济。

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