Reduction of Transition-Metal-Coordinated Carbon Monoxide by a Rare-Earth Hydride Cluster: Isolation of Well-Defined Heteromultimetallic Oxycarbene, Oxymethyl, Carbene, and Methyl Complexes-Reference-Cited by-同舟云学术

Reduction of Transition-Metal-Coordinated Carbon Monoxide by a Rare-Earth Hydride Cluster: Isolation of Well-Defined Heteromultimetallic Oxycarbene, Oxymethyl, Carbene, and Methyl Complexes

Published:2009-10-05 Issue:42 Volume:48 Page:7888-7891
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Takenaka Yasumasa,Shima Takanori,Baldamus Jens,Hou Zhaomin

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference71 articles.

1. Mechanistic features of catalytic carbon monoxide hydrogenation reactions

2. Carbon monoxide and carbon dioxide fixation: relevant C1 and C2 ligand reactions emphasizing (.eta.5-C5H5)Fe-containing complexes

3. For the reduction of carbonyl ligands by main-group-metal hydride reagents, see:

4. Chemistry of the cyclopentadienylmetal carbonyls. VII. Nucleophilic substitution reactions of cyclopentadienyl-iron, -tungsten, and -molybdenum carbonyl cations

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