Department of Chemistry, Dalhousie University, Halifax, Nova Scotia B3H 4J3, Canada.
Angew Chem Int Ed Engl. 2010;49(3):494-512. doi: 10.1002/anie.200904093.
Zwitterionic platinum group metal complexes that feature formal charge separation between a cationic metal fragment and a negatively charged ancillary ligand combine the desirable reactivity profile of related cationic complexes with the broad solubility and solvent tolerance of neutral species. As such, zwitterionic complexes of this type have emerged as attractive candidates for a diversity of applications, most notably involving the breaking and/or forming of E-H and E-C sigma bonds involving a main group element E. Important advances in ancillary ligand design are documented that have enabled the construction of platinum group metal zwitterions. Also summarized are the results of stoichiometric and catalytic investigations in which the reactivity of such zwitterions and their more traditionally employed cationic relatives in sigma bond activation chemistry are compared and contrasted.
同时带有正电荷金属片段和带负电荷的配位体的两性离子铂族金属配合物在保持相关阳离子配合物的反应活性的同时,还兼具中性物种的广泛溶解性和溶剂耐受性。因此,这种两性离子配合物已成为多种应用的有吸引力的候选物,特别是涉及主族元素 E 的 E-H 和 E-Cσ键的断裂和/或形成。本文记录了在辅助配体设计方面的重要进展,这些进展使铂族金属两性离子的构建成为可能。还总结了在这些两性离子和其在σ键活化化学中更常用的阳离子类似物的反应性比较和对比的计量和催化研究的结果。