Organic Chemistry & Catalysis, Debye Institute for Nanomaterials Science, Faculty of Science, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands.
Chemistry. 2011 Jan 3;17(1):42-57. doi: 10.1002/chem.201002508. Epub 2010 Dec 15.
The effects of introducing ionic functionalities in phosphine ligands on the coordination chemistry of these ligands and the catalytic behavior of the corresponding metal complexes are reviewed. The steric and electronic consequences of such functionalizations are discussed. Apart from these steric and electronic effects, the presence of charged groups often leads to additional, supramolecular interactions that occur in the second coordination sphere of the metal complex, such as intramolecular, interligand hydrogen bonding and Coulombic repulsion. These interactions can significantly alter the behavior of the phosphine ligand in question. Such effects have been observed in phosphine-metal association/dissociation equilibria, ligand substitution reactions, and stereoisomerism in phosphine-metal complexes. By drawing general conclusions, this review offers an insight into the coordination and catalytic behavior of phosphine ligands containing ionic functionalities and their corresponding metal complexes.
综述了在膦配体中引入离子官能团对这些配体的配位化学和相应金属配合物的催化行为的影响。讨论了这种官能化的空间和电子后果。除了这些空间和电子效应之外,带电基团的存在通常会导致发生在金属配合物的第二配位层中的额外的超分子相互作用,例如分子内、配体间氢键和库仑排斥。这些相互作用会显著改变所讨论的膦配体的行为。在膦-金属缔合/解离平衡、配体取代反应以及膦-金属配合物的立体异构中观察到了这些效应。通过得出一般性结论,本综述深入了解了含有离子官能团的膦配体及其相应金属配合物的配位和催化行为。