8-10基团(P-N)螯合物过渡金属配合物活化CH键的研究

Vanessa R. Landaeta , Rafael E. Rodríguez-Lugo
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引用次数: 12

摘要

CH键催化活化/功能化一直是人们非常感兴趣的问题,因为这些转化可以从合成的角度建立新的基础,并且可以为有机分子的生产提供替代和更环保的方法。从这个意义上说,开发有效的催化体系来激活CH键变得非常重要,理解控制这种转化的原理,无论是化学计量还是催化,都是必不可少的。从机理或催化的角度研究这些过程需要设计能够进行CH键激活的配体和催化剂。(P,N)螯合物由于其不同给体原子的组合,以及调整其空间和电子特性的能力,以及由于半半性而在金属中心产生潜在的空位,已成为开发新催化体系的替代配体。本文综述了2005年至2015年在含(P,N)螯合配体的8-10基团过渡金属中心活化CH键的研究进展。即使本文描述的使用过渡金属配合物与(P,N)配体激活分子间或分子内CH键的例子尚未参与催化应用,对它们的理解也变得非常重要,并为该领域的未来发展奠定了基础。
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Insights on the CH Bond activation by Transition Metal Complexes from Groups 8–10 Bearing (P-N) Chelates

CH bond catalytic activation/functionalization has been matter of great interest, since these transformations could establish new grounds from the synthetic perspective, and could serve to propose alternative and greener methods for the production of organic molecules. In this sense, the development of efficient catalytic systems for CH bond activation becomes of great importance, and understanding the principles that govern such transformations, either stoichiometric or catalytic, is essential. To study such processes from the mechanistic or catalytic point of view requires of the design of ligands and catalysts able of performing CH bond activation. (P,N)-chelates have arisen as alternative ligands to develop new catalytic systems, due to their combination of different donor atoms, and the ability to tune their steric and electronic characteristics and to create potential vacant sites at the metal center due to hemilability.

This mini review summarizes the advances from 2005 to 2015 in the field of CH bond activation at transition metal centers from groups 8–10 bearing (P,N)-chelating ligands. Even when the examples of inter- or intramolecular CH bond activation using transition metal complexes with the (P,N) ligands described herein do not engage yet in catalytic applications, their understanding becomes of great importance and sets the basis for future developments in this field.

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2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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