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Comparative study of ring-opening polymerization of L-lactide and epsilon-caprolactone using zirconium hexadentate bis(aminophenolate) complexes as catalysts

机译:六齿锆双(氨基酚盐)配合物催化L-丙交酯和ε-己内酯开环聚合的比较研究

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摘要

A series of zirconium bis(aminophenolate) complexes as catalysts for the ring opening polymerization of L-lactide (LA) and epsilon-caprolactone (CL) were investigated. Ligands bearing various chelating groups have a profound influence on the catalysis results. Among them, the thiophen-2-yl methyl group showed the greatest activity while the pyridine-2-yl methyl group showed the worst performance with regard to the rate of CL polymerization. However, the trend was reversed for the rate of LA polymerization. The kinetic results indicated a first-order dependency on [CL] and [LA]. However, the order of the catalyst concentration was different. Polymerization proceeded with second-order dependence on [(LZr)-Zr-OMe(OBn)(2)] for CL but with first-order dependence on [(LZr)-Zr-OMe(OBn)(2)] for LA.
机译:研究了一系列双(氨基酚酸)锆配合物,用于L-丙交酯(LA)和ε-己内酯(CL)的开环聚合。带有各种螯合基团的配体对催化结果有深远的影响。其中,就CL聚合速率而言,噻吩-2-基甲基表现出最大的活性,而吡啶-2-基甲基表现出最差的性能。但是,LA聚合速率的趋势相反。动力学结果表明对[CL]和[LA]具有一阶依赖性。但是,催化剂浓度的顺序不同。对于CL而言,聚合反应对[[LZr)-Zr-OMe(OBn)(2)]具有二阶依赖性,但对于LA而言,聚合对[[LZr)-Zr-OMe(OBn)(2)]具有一阶依赖性。

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