Abstract

Abstract Photochemical degradation of a series of tin-manganese bonded complexes was studied. The apparent reactivity of the tin-manganese bond toward UV irradiation is interpreted on the basis of absorption spectra of relevant complexes and available emissions from the light source. Two kinds of orthometalated products were obtained from photolysis of Me3Sn–Mn(CO)3[P(OPh)3]2 in benzene. Various kinds of experiments suggest that their photochemical reactions proceed through homolytic cleavage of the Sn–Mn bond in the initial stage and the resulting 15-electron intermediates abstract hydrogen from the triphenyl phosphite moiety. Molecular structures of the two kinds of orthometalated products, as clarified by X-ray structure analyses, are described.

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