Abstract

The use of carbonyl complexes in homogeneous and heterogeneous catalysis is very briefly presented. The demonstrated and expected advantages of such catalysts and the knowledge-gap in these areas of research are highlighted. The results obtained in the author’s laboratory, for two specific reactions — the carbonylation of nitrobenzene and transfer hydrogenation of organic carbonyl compounds with ruthenium carbonyl clusters as catalysts — are discussed. Where empirical and rigorous kinetic analyses are not possible, the usefulness of building hypothetical catalytic cycles with fully characterised clusters to rationalise observed activity and/or selectivity is emphasised. A summary of recent work on organic polymer supported mono- and polynuclear metal carbonyls is also presented.

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