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Electrochemical study of σ-bonds in π-complexes of transition metals

Communication 2. Polarographic reduction of π-C5H5Fe(CO)2-σ-R and related compounds

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

Conclusions

  1. 1.

    The mechanism of the polarographic reduction of π-complexes of iron with the composition π-C5H5Fe(CO) (L)-σ-R [L=CO, P(C6H5)3 or P(OC6H5)3], containing Fe- C σ- bonds of various types, on a dropping mercury electrode was studied.

  2. 2.

    The influence of substiturnts in the p-position of the phenyl ring (R=C6H4-X) is described by aromatic polar substituent constants σp o, which is evidence of a weak polar influence of substituents upon the transition state of the electrochemical reaction studied.

  3. 3.

    The ease of reduction of the Fe-C σ-bond depends upon the stability of the carbanion formed and varies parallel with its basicity.

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The article is published on the basis of a resolution of the Conference of Editors-in-Chief of the Journals of the Academy of Sciences of the USSR, from July 12, 1962, as the dissertation work of L. I. Denisovich.

Deceased.

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2378–2384, November, 1967.

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Denisovich, L.I., Gubin, S.P. & Chapovskii, Y.A. Electrochemical study of σ-bonds in π-complexes of transition metals. Russ Chem Bull 16, 2271–2275 (1967). https://doi.org/10.1007/BF00911825

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  • DOI: https://doi.org/10.1007/BF00911825

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