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Facile synthesis and catalytic activity of welldefined amphiphilic block copolymers based on N-vinylimidazolium

机译:基于N-乙烯基咪唑的定义明确的两亲嵌段共聚物的合成与催化活性

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摘要

Well-defined amphiphilic block copolymers, poly(styrene)-b-poly(N-vinylimidazole) (PS-b-PVim), were successfully synthesized by macromolecular design via interchange of the xanthates/reversible addition-fragmentation chain transfer (RAFT) polymerization. The structure of the copolymer based on Vim can be well controlled, and the molecular weight distribution was relatively narrow (PDI = 1.24). The size and morphology of the aggregates of the amphiphilic copolymers were investigated by dynamic light scattering and transmission electron microscope, the results implied that the uniform spheroidal micelles consisting of PS core and PVim corona were assembled, and the catalytic activities of PS-b-PVim for the hydrolysis of p-nitrophenyl acetate at different temperatures were also investigated by high-performance liquid chromatograph (HPLC); the catalytic activities of diblock copolymers were prominently improved compared with that of PVim homopolymers. Moreover, the catalytic activities of the copolymers followed the Arrhenius behavior in the wide experimental temperature range.
机译:通过黄原酸酯交换/可逆加成-断裂链转移(RAFT)聚合反应,通过大分子设计成功合成了定义明确的两亲嵌段共聚物,聚苯乙烯-b-聚N-乙烯基咪唑。可以很好地控制基于Vim的共聚物的结构,并且分子量分布相对较窄(PDI = 1.24)。通过动态光散射和透射电子显微镜研究了两亲共聚物的团聚体的尺寸和形貌,结果表明组装了由PS核和PVim电晕组成的均匀球形胶束,并且PS-b-PVim具有催化活性。还通过高效液相色谱(HPLC)研究了在不同温度下乙酸对硝基苯酯的水解作用;与PVim均聚物相比,二嵌段共聚物的催化活性显着提高。此外,在宽的实验温度范围内,共聚物的催化活性遵循Arrhenius行为。

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