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Hydrazones

XXXIX. Polarographic study of N-benzylideneiminopyridinium iodides

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The polarographic behavior of a number of N-benzylideneiminopyridinium iodides in aqueous alcohol buffer solutions was studied over a wide range of pH values. The mechanism of their reduction on a dropping mercury electrode and the factors affecting the cleavage of the N-N bond are discussed. The reduction product-the pyridinium ion-induces the catalytic evolution of hydrogen.

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Literature cited

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Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry, Academy of Sciences of the USSR, Kazan'

    Yu. P. Kitaev, T. V. Troepol'skaya & L. N. Orlova

Authors
  1. Yu. P. Kitaev
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  2. T. V. Troepol'skaya
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  3. L. N. Orlova
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Additional information

See [1] for communication XXXVIII.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 666–669, May, 1974.

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Kitaev, Y.P., Troepol'skaya, T.V. & Orlova, L.N. Hydrazones. Chem Heterocycl Compd 10, 576–578 (1974). https://doi.org/10.1007/BF00471331

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  • DOI: https://doi.org/10.1007/BF00471331

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