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膦酰亚胺钇配合物:丙交酯聚合的高活性和立体选择性引发剂。

Phosphasalen yttrium complexes: highly active and stereoselective initiators for lactide polymerization.

机构信息

Laboratoire Hétéroéléments et Coordination, Ecole Polytechnique, CNRS, 91128 Palaiseau Cedex, France.

出版信息

Inorg Chem. 2012 Feb 20;51(4):2157-69. doi: 10.1021/ic202015z. Epub 2012 Feb 7.

Abstract

Preparation and characterization of three yttrium alkoxide complexes with new phosphasalen ligands are reported. The phosphasalens are analogues of the well-known salen ligands but with iminophosphorane donors replacing the imine functionality. The three yttrium alkoxide complexes show mono- and dinuclear structures in the solid state, depending on the substituents on the ligand. The new ligands and complexes are characterized using multinuclear NMR spectroscopy, mass spectrometry, elemental analysis, and single-crystal X-ray diffraction experiments. The complexes are all rapid initiators for lactide polymerization; they show excellent polymerization control on addition of exogeneous alcohol. The mononuclear complex shows extremely rapid rates and a high degree of stereocontrol in rac-lactide polymerization, yielding heterotactic PLA (P(s) of 0.9). The phosphasalens are, therefore, excellent ligands for lactide ring-opening polymerization catalysis showing superior rates and stereocontrol versus salen ligands, which may be related to their excellent donating ability and the high degrees of steric protection they can confer.

摘要

本文报道了三种新型膦亚胺水杨醛钇配合物的制备和性质研究。膦亚胺水杨醛配体是熟知的水杨醛配体的类似物,但其亚胺官能团被亚磷酰胺供体所取代。这三种水杨醛钇配合物在固态中呈现单核和双核结构,这取决于配体上的取代基。通过多核 NMR 光谱、质谱、元素分析和单晶 X 射线衍射实验对新配体和配合物进行了表征。这些配合物均是丙交酯聚合的快速引发剂,在外加醇的作用下表现出优异的聚合控制性能。单核配合物在 rac-丙交酯聚合中表现出非常快的反应速率和高度的立构控制,得到了具有异质结构的 PLA(P(s) 为 0.9)。因此,这些膦亚胺水杨醛配体是丙交酯开环聚合催化的优良配体,与水杨醛配体相比,它们具有更高的反应速率和立构控制能力,这可能与其优异的供电子能力和提供的高立体保护程度有关。

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