Outer sphere hydrogenation catalysis

被引:155
作者
Eisenstein, Odile [1 ]
Crabtree, Robert H. [2 ]
机构
[1] Univ Montpellier 2, Inst Charles Gerhardt, CNRS, UMR 5253, F-34095 Montpellier, France
[2] Yale Univ, Dept Chem, New Haven, CT 06520 USA
关键词
HYDROXYCYCLOPENTADIENYL RUTHENIUM HYDRIDE; FRUSTRATED LEWIS PAIRS; ASYMMETRIC TRANSFER HYDROGENATION; TRANSITION-METAL HYDRIDES; N-HETEROCYCLIC CARBENE; PRIMARY AMINE DONOR; CARBON-DIOXIDE; HOMOGENEOUS HYDROGENATION; DIHYDROGEN ACTIVATION; IONIC HYDROGENATION;
D O I
10.1039/c2nj40659d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the title catalysts, the substrate, typically a ketone, imine or N-heterocycle, remains in the outer sphere (OS). The catalyst transfers hydride and a proton to the unbound substrate either by a concerted or by a stepwise path. These include catalysts not always considered together, such as Bullock's ionic hydrogenation catalysts, bifunctional catalysts in the tradition of Shvo and Noyori and Stephan's frustrated Lewis pair catalysts. By omitting the oxidative addition, insertion and reductive elimination pathways of conventional inner sphere (IS) catalysts, these OS pathways are in principle equally open to inexpensive metals and even nonmetal catalysts. These OS pathways lead to useful selectivity properties, particularly Noyori's asymmetric catalysis, but much more remains to be done in this rapidly developing field.
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页码:21 / 27
页数:7
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