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第三到第五族金属烷基配合物催化的未活化 C-H 键的直接官能化。

Direct functionalization of unactivated C-H bonds catalyzed by group 3-5 metal alkyl complexes.

机构信息

Department of Chemistry, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan.

出版信息

Dalton Trans. 2014 Feb 14;43(6):2331-43. doi: 10.1039/c3dt52758a. Epub 2013 Dec 12.

Abstract

This perspective summarizes direct C-H bond functionalization reactions catalyzed by group 3-5 metal alkyl complexes. Metal-carbon bonds of group 3-5 metals have potentially high reactivity toward both C-H bond activation reactions through the intrinsic σ-bond metathesis pathway and insertion of unsaturated organic molecules. Upon the combination of these two elemental steps, direct C-H bond functionalization reactions of (hetero)aromatic compounds, methane, alkylamines, and terminal alkynes, proceed through C(sp)-H, C(sp(2))-H, and C(sp(3))-H bond activation reactions. Here we review as catalysts for these transformations not only simple metallocene complexes but also non-metallocene complexes supported by a variety of ligands, which are often superior in terms of catalyst design and catalytic activity.

摘要

这篇观点综述总结了第 3-5 族金属烷基配合物催化的直接 C-H 键功能化反应。第 3-5 族金属的金属-碳键对于 C-H 键活化反应(通过固有的σ键复分解途径)和不饱和有机分子的插入具有潜在的高反应性。通过这两个基本步骤的结合,(杂)芳族化合物、甲烷、烷基胺和末端炔烃的直接 C-H 键功能化反应通过 C(sp)-H、C(sp(2))-H 和 C(sp(3))-H 键活化反应进行。在这里,我们不仅综述了作为这些转化催化剂的简单茂金属配合物,还综述了由各种配体支持的非茂金属配合物,就催化剂设计和催化活性而言,这些配合物通常更优越。

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