ME and M=E complexes of iron and cobalt that emphasize three-fold symmetry (EO, N, NR)

被引:166
作者
Saouma, Caroline T. [1 ]
Peters, Jonas C. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
Atom and group transfer; Metal-to-ligand multiple bond; Oxos; Imides; Nitrides; C-H ACTIVATION; SPIN OXOIRON(IV) COMPLEX; NITROGEN ATOM-TRANSFER; RAY CRYSTAL-STRUCTURE; METAL-OXO COMPLEXES; ELECTRONIC-STRUCTURE; IMIDO COMPLEXES; SPECTROSCOPIC CHARACTERIZATION; MOLECULAR-STRUCTURE; NITRENE TRANSFER;
D O I
10.1016/j.ccr.2011.01.009
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Mid-to-late transition metal complexes that feature terminal, multiply bonded ligands such as oxos, imides, and nitrides have been invoked as intermediates in several catalytic transformations of synthetic and biological significance. Until about ten years ago, isolable examples of such species were virtually unknown. Over the past decade or so, numerous chemically well-defined examples of such species have been discovered. In this context, the present review summarizes the development of 4- and 5-coordinate Fe(E) and Co(E) species under local three-fold symmetry. (C) 2011 Elsevier By. All rights reserved.
引用
收藏
页码:920 / 937
页数:18
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