Issue 11, 1991

Synthesis, structure and isomerism of [Mn2(µ-PPhR)2(CO)8](R = H, alkyl, acyl or carboxylate); crystal structures of trans-[Mn2(µ-PPhR)2(CO)8](R = H or COMe)

Abstract

The thermal reaction of [Mn2(CO)10] with PPhH2 in undried decalin at 150 °C gives [Mn2(µ-PPhH)2(CO)8] as a cistrans mixture of isomers. Recrystallisation enables the trans isomer to be separated from this mixture and the structure of this isomer has been determined by X-ray diffraction analysis. The trans isomer is configurationally stable in toluene at room temperature but isomerises in more polar solvents or on heating. Possible mechanisms for this isomerisation are investigated. Deprotonation of [Mn2(µ-PPhH)2(CO)8] followed by treatment with a range of organic halides, RX, gives the complexes [Mn2(µ-PPhR)2(CO)8] which also exhibit cistrans isomerism in solution. Recrystallisation of one of these complexes, [Mn2(µ-PPhCOMe)2(CO)8], gives the trans isomer, the structure of which has also been determined by X-ray analysis.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1991, 3097-3102

Synthesis, structure and isomerism of [Mn2(µ-PPhR)2(CO)8](R = H, alkyl, acyl or carboxylate); crystal structures of trans-[Mn2(µ-PPhR)2(CO)8](R = H or COMe)

M. P. Brown, J. Buckett, M. M. Harding, R. M. Lynden-Bell, M. J. Mays and K. W. Woulfe, J. Chem. Soc., Dalton Trans., 1991, 3097 DOI: 10.1039/DT9910003097

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