Element-Ligand Cooperativity with p-Block Elements

被引:78
|
作者
Greb, Lutz [1 ]
Ebner, Fabian [1 ]
Ginzburg, Yael [1 ]
Sigmund, Lukas M. [1 ]
机构
[1] Heidelberg Univ, Anorgan Chem Inst, Neuenheimer Feld 275, D-69120 Heidelberg, Germany
关键词
Metal-ligand cooperativity; Frustrated Lewis pairs; Bond activation; P-Block elements; Homogeneous catalysis; FRUSTRATED-LEWIS-PAIR; H BOND ACTIVATION; REDOX-ACTIVE LIGANDS; MAIN-GROUP ELEMENTS; CYCLOADDITION REACTIONS; CATALYTIC-REDUCTION; OXIDATIVE ADDITION; REVERSIBLE BINDING; GALLIUM COMPLEXES; TERMINAL ALKYNES;
D O I
10.1002/ejic.202000449
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Metal-ligand cooperativity (MLC) had a tremendous impact on d-block metal-mediated bond activation and homogeneous catalysis. Is this concept translatable to the elements of the p-block? Are there analogies already at hand? In this review, we describe contributions in which a p-block element (group 13-15) and its ligand (surrounding molecular framework) operate synergistically in a substrate activation or a catalytic cycle. This activity is termed element-ligand cooperativity (ELC), in correspondence to MLC. After the concepts of p-block low-valent states and frustrated Lewis pairs mimicking the ambiphilic reactivity of transition metals, the spatial proximity of nucleophilic and electrophilic reaction sites and a small HOMO-LUMO gap in a p-block ELC complex might offer yet another approach. Selected examples shall illustrate common reactivities of ELC, disclose conceptual analogies with d-block MLC, and outline shortcomings in this field.
引用
收藏
页码:3030 / 3047
页数:18
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