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Spectrometric study of some N-substituted 3(5)-methylpyrazoles and their complexes with cupric chloride

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It follows from a comparison of the IR spectra of 1-substituted 3(5)-methylpyrazoles and their complexes with cupric chloride that coordination of the metal is realized through the unshared pair of electrons of the nitrogen atom of the C=N bond.

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Authors and Affiliations

  1. North Donetsk Branch of the State Scientific-Research Institute of the Nitrogen Industry and Products of Organic Synthesis, USSR

    Ya. A. Shuster, V. A. Kozlova & V. I. Seraya

Authors
  1. Ya. A. Shuster
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  2. V. A. Kozlova
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  3. V. I. Seraya
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1655–1659, December, 1974.

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Shuster, Y.A., Kozlova, V.A. & Seraya, V.I. Spectrometric study of some N-substituted 3(5)-methylpyrazoles and their complexes with cupric chloride. Chem Heterocycl Compd 10, 1455–1458 (1974). https://doi.org/10.1007/BF00474328

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  • DOI: https://doi.org/10.1007/BF00474328

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