Metal-Ligand Cooperation

被引:1007
作者
Khusnutdinova, Julia R. [2 ]
Milstein, David [1 ]
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
[2] Okinawa Inst Sci & Technol, Coordinat Chem & Catalysis Unit, Onna Son, Okinawa 9040495, Japan
基金
欧洲研究理事会; 以色列科学基金会;
关键词
cooperating ligands; homogeneous catalysis; metal complexes; N-HETEROCYCLIC CARBENE; ASYMMETRIC TRANSFER HYDROGENATION; C-H ACTIVATION; HYDROXYCYCLOPENTADIENYL RUTHENIUM HYDRIDE; ISOTOPE EFFECT EVIDENCE; PNP PINCER COMPLEXES; BOND-ACTIVATION; CATALYTIC-HYDROGENATION; IRON CATALYSTS; DIHYDROGEN ACTIVATION;
D O I
10.1002/anie.201503873
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-ligand cooperation (MLC) has become an important concept in catalysis by transition metal complexes both in synthetic and biological systems. MLC implies that both the metal and the ligand are directly involved in bond activation processes, by contrast to "classical" transition metal catalysis where the ligand (e.g. phosphine) acts as a spectator, while all key transformations occur at the metal center. In this Review, we will discuss examples of MLC in which 1) both the metal and the ligand are chemically modified during bond activation and 2) bond activation results in immediate changes in the 1st coordination sphere involving the cooperating ligand, even if the reactive center at the ligand is not directly bound to the metal (e.g. via tautomerization). The role of MLC in enabling effective catalysis as well as in catalyst deactivation reactions will be discussed.
引用
收藏
页码:12236 / 12273
页数:38
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