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Reaction of crown ethers with five-membered heterocycles: 1H-imidazole-4,5-dicarbonitrile, 3-nitro-1,2,4-triazole, and 1H-tetrazole

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

By the reaction of 1H-imidazole-4,5-dicarbonitrile, 3-nitro-1,2,4-triazole, and 1H-tetrazole, containing one proton at each of the two proton-donating atoms separated by one covalent bond, it was shown that uncharged crystalline supramolecular compounds can be obtained on account of the proton-donating characteristics of the aromatic heterocycles.

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Authors and Affiliations

  1. Tamkang University, Taipei, 25137, Taiwan (Chinese Republic)

    Wen Jwu Wang & San Wei Tang

  2. Odessa State Ecological University, Ministry of Education and Science of Ukraine, Odessa, 65016

    E. V. Ganin

Authors
  1. Wen Jwu Wang
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  2. San Wei Tang
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  3. E. V. Ganin
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__________

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1302–1305, September, 2006.

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Wang, W.J., Tang, S.W. & Ganin, E.V. Reaction of crown ethers with five-membered heterocycles: 1H-imidazole-4,5-dicarbonitrile, 3-nitro-1,2,4-triazole, and 1H-tetrazole. Chem Heterocycl Compd 42, 1126–1129 (2006). https://doi.org/10.1007/s10593-006-0215-y

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  • DOI: https://doi.org/10.1007/s10593-006-0215-y

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