Metal-Ligand Cooperation at Phosphine-Based Acceptor Pincer Ligands

被引:6
|
作者
Tiddens, Martine R. [1 ]
Moret, Marc-Etienne [1 ]
机构
[1] Univ Utrecht, Fac Sci, Debye Inst Nanomat Sci, Organ Chem & Catalysis, Utrecht, Netherlands
基金
欧洲研究理事会;
关键词
Acceptor ligands; Ambiphilic ligands; Bond activation; Cooperative catalysis; Metal-ligand cooperation; Pincer; pi-Ligands; C-H ACTIVATION; COORDINATION CHEMISTRY; CATALYTIC-HYDROGENATION; WATER ELIMINATION; CARBENE COMPLEXES; NICKEL-COMPLEXES; BOND ACTIVATION; RHODIUM COMPLEX; KETONE LIGAND; LEWIS-ACIDS;
D O I
10.1007/3418_2020_70
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Acceptor ligands, which predominantly withdraw electron density from a transition metal center, often engage in weak metal-ligand interactions. These can be stabilized by flanking the acceptor moiety with strongly binding phosphines in a pincer motif, affording more robust complexes in which bond activation and/or bond-forming events can take place while preserving the integrity of the molecule as a whole. This contribution highlights recent developments in this area. Compounds incorporating a borane at the central position are discussed first, followed by compounds incorporating an electrophilic C = E (E = C, O, N) p-bond. In both cases, recent examples highlight the ability of these ligands to (1) respond to electronic changes at the metal by modifying their binding mode and (2) accept a nucleophilic fragment (e.g., hydride) from substrate molecules. Applications of acceptor pincer ligands as cooperative catalysts are discussed.
引用
收藏
页码:25 / 69
页数:45
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