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Orienting effect of the carboxylate group in the system of cyclopentadienyl-manganese tricarbonyl

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Conclusions

  1. 1.

    The influence of the carboxylate group upon the reactivity of theα- andβ-positions in the system of cyclopentadienylmanganesetricarbonyl in the reaction of protophilic substitution was studied.

  2. 2.

    The factors of the partial rates of isotopic exchange of hydrogen for theα- andβ-positions were found by a combination of methods of isotopic exchange of hydrogen and proton resonance.

  3. 3.

    Under these conditions, the reactivity of theα-position is almost three times as great as that of theβ-position.

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Literature cited

  1. 1.

    L. M. Shen, G. G. Long, and C. G. Moreland, J. Organometal. Chem. April, No. 5, 362 (1966).

  2. 2.

    A. N. Nesmeyanov, D. N. Kersanov, V. N. Setkina, N. V. Kislyakova, N. E. Kolobova, and K. N. Anisimov, Izv. AN SSSR. Ser. Khimicheskaya,1966, 944.

  3. 3.

    G. E. Hall, R. Piccolini, and J. D. Roberts, J. Amer. Chem. Soc.,77, 4540 (1955).

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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 915–916, April, 1967.

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Kursanov, D.N., Setkina, V.N., Kislyakova, N.V. et al. Orienting effect of the carboxylate group in the system of cyclopentadienyl-manganese tricarbonyl. Russ Chem Bull 16, 881–882 (1967). https://doi.org/10.1007/BF00915678

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Keywords

  • Hydrogen
  • Carboxylate
  • Carboxylate Group
  • Isotopic Exchange
  • Proton Resonance