Conclusions
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1.
As a result of chemical and electrochemical reduction the authors convert linear trinuclear osmium carbonyl halides to triangulo-dodecacarbonyl triosmium.
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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.
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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