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Synthesis and Characterization of N,N,O-Tridentate Aminophenolate Zinc Complexes and Their Catalysis in the Ring-Opening Polymerization of Lactides

机译:N,N,O-三叉型氨基酚盐锌配合物的合成,表征及其在丙交酯开环聚合中的催化作用

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摘要

A series of aminophenolate ligands with various pendant groups and associated ethyl Zn complexes were synthesized and studied as catalysts for the ring-opening polymerization (ROP) of lactides (LAs). The thiophenylmethyl group (L4ZnEt) increased the catalytic activity more than the benzyl group (L1ZnEt) did, and 2-fluorobenzyl (L3ZnEt) and 2-methoxybenzyl (L2ZnEt) groups had the opposite effect. In addition, the LA polymerization mechanism proved by Nuclear Magnetic Resonance and Density Function Theory was that LA was attracted by H···O bond of an α-hydrogen of the LA molecule and the phenoxyl oxygen of the catalyst. After the dissociation of amino group from the Zn atom, the benzyl alcohol initiated LA without replacing the ethyl group of Zn complex. It is the first case where the ethyl group is regarded as a ligand and cannot be replaced by benzyl alcohol, and this information is very important for the mechanism study of ROP.
机译:合成了一系列具有各种侧基的氨基酚盐配体和相关的乙基锌配合物,并研究了它们作为丙交酯(LAs)开环聚合(ROP)的催化剂。硫代苯甲基( L 4 ZnEt )的催化活性比苄基( L 1 ZnEt )和2-氟苄基( L 3) ZnEt )和2-甲氧基苄基( L 2 ZnEt < / strong>)的效果相反。另外,由核磁共振和密度泛函理论证明的LA聚合机理是LA被LA分子的α-氢的H··O键和催化剂的苯氧基所吸引。从Zn原子上解离氨基后,苯甲醇引发LA,而没有取代Zn络合物的乙基。这是乙基被视为配体且不能被苄醇取代的第一种情况,该信息对于ROP的机理研究非常重要。

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