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硅取代烯丙基配体的配位化学。

The coordination chemistry of silyl-substituted allyl ligands.

机构信息

School of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.

出版信息

Dalton Trans. 2010 Mar 14;39(10):2469-83. doi: 10.1039/b918619k. Epub 2009 Dec 17.

Abstract

Metal allyl complexes in which the ligands carry bulky silyl substituents frequently show stability that cannot be achieved with unsubstituted analogues. As a result, it has been possible to characterize a large family of structurally diverse metal silyl-allyls from the s-, p-, d- and f-blocks of the Periodic Table, and to study the coordination chemistry of compounds that often have no counterparts without bulky substituents. The fact that the majority of compounds discussed in this Perspective have been published since 2000 reflects the newness of the area, and the article summarizes the main developments in the structural chemistry of metal silyl-allyls and also selected synthetic and catalytic applications. Although organometallic chemistry is often regarded as transcending traditional boundaries between 'organic' and 'inorganic' chemistry, an understanding persists that those working in the field can be labelled 'inorganic organometallic' chemists or 'organic organometallic' chemists. It is hoped that chemists from a broad range of backgrounds will be able to use this review as an entry point to an exciting new direction in metal allyl chemistry.

摘要

含有大体积硅取代基的金属烯丙基配合物通常具有无法用未取代类似物实现的稳定性。因此,已经有可能从元素周期表的 s、p、d 和 f 区中对大量结构多样的金属硅烯丙基配合物进行了表征,并研究了通常没有大取代基的化合物的配位化学。这一事实反映了该领域的新颖性,本观点文章总结了金属硅烯丙基配合物的结构化学的主要发展以及一些选定的合成和催化应用。尽管金属有机化学通常被认为超越了“有机”和“无机”化学之间的传统界限,但人们仍然认为,该领域的工作者可以被标记为“无机金属有机”化学家或“有机金属有机”化学家。希望来自广泛背景的化学家能够将这篇综述用作进入金属烯丙基化学令人兴奋的新方向的切入点。

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