The power of electron paramagnetic resonance to study asymmetric homogeneous catalysts based on transition-metal complexes

被引:17
作者
Van Doorslaer, S. [1 ]
Caretti, I. [1 ]
Fallis, I. A. [2 ]
Murphy, D. M. [2 ]
机构
[1] Univ Instelling Antwerp, Dept Phys, B-2610 Antwerp, Belgium
[2] Cardiff Univ, Sch Chem, Cardiff CF10 3AT, S Glam, Wales
基金
英国工程与自然科学研究理事会;
关键词
Electron paramagnetic resonance spectroscopy; Electron spin-echo envelope modulation spectroscopy; Electron nuclear double resonance spectroscopy; Asymmetric catalysis; METHYL-COENZYME-M; M-REDUCTASE; PULSE EPR; CONTINUOUS-WAVE; ENDOR SPECTROSCOPY; COPPER(II) COMPLEXES; KINETIC RESOLUTION; OFF COB(II)ALAMIN; METHANE FORMATION; FROZEN-SOLUTIONS;
D O I
10.1016/j.ccr.2008.12.010
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Asymmetric synthesis involves the preparation of chiral compounds with well-defined three-dimensional molecular structure or stereochemistry. Many of these enantioselective transformations involve chiral ligands incorporating transition-metal ions. Over the years numerous synthetic, spectroscopic and theoretical approaches have been applied to understand and probe the inner workings and mode of chiral transfer in these homogeneous based catalysts. For the paramagnetic based asymmetric complexes, electron paramagnetic resonance (EPR) can provide a wealth of detail and information on the structure and mechanism of the catalysts. Despite this potential, the application and uptake of advanced EPR methodologies to this field of endeavor has been limited. The purpose of this review is to explain and illustrate, through representative examples, the enormous amount of information that can be obtained from an EPR study of the chiral metal-based complexes, ranging from electronic structure and symmetry to spatial arrangement of interacting ligands and substrates. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:2116 / 2130
页数:15
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