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Induction and resonance constants of butadienyliron tricarbonyl substituents

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

Conclusions

In dieneiron tricarbonyls the π-electron density in the 1 position of the coordinated butadiene system is higher than in the 2 position, while the σ-electron density is distributed uniformly.

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Literature cited

  1. N. S. Nametkin, A. I. Nekhaev, and V. D. Tyurin, Izv. Akad. Nauk SSSR, Ser. Khim., 890 (1974).

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Authors and Affiliations

  1. A. V. Topchiev Institute of Petrochemical Synthesis, Academy of Sciences of the USSR, Moscow

    N. S. Nametkin, A. I. Nekhaev, S. P. Gubin & V. D. Tyurin

  2. I. M. Gubkin Moscow Institute of the Petrochemical and Gas Industry, USSR

    N. S. Nametkin, A. I. Nekhaev, S. P. Gubin & V. D. Tyurin

Authors
  1. N. S. Nametkin
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  2. A. I. Nekhaev
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  3. S. P. Gubin
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  4. V. D. Tyurin
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1636–1638, July, 1976.

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Nametkin, N.S., Nekhaev, A.I., Gubin, S.P. et al. Induction and resonance constants of butadienyliron tricarbonyl substituents. Russ Chem Bull 25, 1552–1553 (1976). https://doi.org/10.1007/BF00920843

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  • DOI: https://doi.org/10.1007/BF00920843

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