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Metal-chain-metal-ring transitions in the reduction of trinuclear osmium carbonyl halides

  • Inorganic Chemistry
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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

  1. 1.

    As a result of chemical and electrochemical reduction the authors convert linear trinuclear osmium carbonyl halides to triangulo-dodecacarbonyl triosmium.

  2. 2.

    They study the polarographic reduction of linear compounds of osmium of the type X2Os3(CO)12 (X=Cl, Br, I). In contrast with C-X bonds in dihaloalkanes, dissociation of Os-X bonds involves a one-electron stage and leads to the formation of osmium carbonyl radicals which are subsequently converted into metal rings.

  3. 3.

    The ease of reduction of compounds of the type X2Os3(CO)12 depends on the electronegativity of the halogen atoms, and increases in the order X=Cl<Br<I.

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2423–2428, November, 1981.

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Gubin, S.P., Trukhacheva, V.A., Burmakina, G.V. et al. Metal-chain-metal-ring transitions in the reduction of trinuclear osmium carbonyl halides. Russ Chem Bull 30, 1997–2001 (1981). https://doi.org/10.1007/BF01094616

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  • DOI: https://doi.org/10.1007/BF01094616

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