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Organocobalt chemistry : ウィキペディア英語版
Organocobalt chemistry
Organocobalt chemistry is the chemistry of organometallic compounds containing a carbon to cobalt chemical bond. Organocobalt compounds are involved in several organic reactions and the important biomolecule vitamin B12 has a cobalt-carbon bond. Many organocobalt compounds exhibit useful catalytic properties, the preeminent example being dicobalt octacarbonyl. An early example of organocobalt chemistry is the carbonylation of azobenzene with dicobalt octacarbonyl as described by Murahashi & Horiie in 1956:
==Carbonyl complexes==
Dicobalt octacarbonyl reacts with hydrogen and alkenes to give aldehydes. This reaction is the basis of hydroformylation, the formation of aldehydes from an alkene, CO and hydrogen. A key intermediate is cobalt tetracarbonyl hydride (HCo(CO)4). The original Ruhrchemie process produced propanal from ethene and syngas using cobalt carbonyl has been displaced by rhodium-based catalysts. Processes involving cobalt are practiced by BASF, EXXON, and Shell mainly for the production of C7-C14 alcohols used for the production of surfactants.〔Boy Cornils, Wolfgang A. Herrmann, Chi-Huey Wong, Horst -Werner Zanthoff: ''Catalysis from A to Z: A Concise Encyclopedia'', 2408 Seiten, Verlag Wiley-VCH Verlag GmbH & Co. KGaA, (2012), ISBN 3-527-33307-X.〕
In hydrocarboxylations hydrogen is replaced by water or an alcohol and the reaction product is a carboxylic acid or an ester. An example of this reaction type is the conversion of butadiene to adipic acid.

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