中性NNNN大环的活性主族金属配合物,Me4TACD

IF 3.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Jun Okuda, Priyabrata Ghana, Louis J. Morris
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引用次数: 0

摘要

目前,人们对引入具有分子定义的主族金属化合物作为各种键解理和成键转化的均相催化剂的前体和模式配合物有相当大的兴趣。本文以NNNN大环配体Me4TACD (N,N ',N ',N ' -四甲基-1,4,7,10-四氮杂环十二烷)为重点,综述了Me4TACD在稳定活性主基团s-和p-嵌段(1,2,12 -14族)金属方面的多功能性。金属氢化物、烃基和硅基通常是单体的,可以催化烯烃的加氢官能化。与使用大量配体的d-和f-嵌段过渡金属的丰富配位化学相反,主基团金属仍然为新的反应留下了空间,与目前发展对s-和p-嵌段金属配体组合的系统理解相一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reactive Main Group Metal Complexes of the Neutral NNNN Macrocycle, Me4TACD
Currently, there is considerable interest in introducing molecularly defined main group metal compounds as precursors and model complexes of homogeneous catalysts for various bond cleavage and forming transformations. With a focus on the NNNN macrocyclic ligand Me4TACD (N,N’,N’’,N’’’-tetramethyl-1,4,7,10-tetraazacyclododecane), this review summarizes the versatility of the ligand Me4TACD for the stabilization of reactive main group s- and p-block (group 1, 2, 12-14) metals. Metal hydrides, hydrocarbyls and silyls are often monomeric and catalyze alkene hydrofunctionalisations. In contrast to the rich coordination chemistry of d- and f-block transition metals using a plethora of ligands, main group metals still leave room for new reactivities, aligning with the current efforts to develop a systematic understanding in s- and p-block metal-ligand combinations.
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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