REACTION OF CROWN ETHERS WITH FIVE-MEMBERED HETEROCYCLES: 1H-IMIDAZOLE-4,5-DICARBONITRILE, 3-NITRO-1,2,4-TRIAZOLE, AND 1H-TETRAZOLE

Authors

  • Вен-Дзву Ванг Tamkang University, Taipei 25137
  • Сан-Вей Танг Tamkang University, Taipei 25137
  • Э. В. Ганин Odessa State Ecological University, Ministry of Education and Science of Ukraine, Odessa 65016

DOI:

https://doi.org/10.1007/7807

Keywords:

1H-imidazole-4, 5-dicarbonitrile, 3-nitro-1, 2, 4-triazole, 1H-tetrazole, crown ethers, crystalline supramolecular compounds

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.

How to Cite
Wang, W. J.; Tang, S. W.; Ganin, E. V. Chem. Heterocycl. Compd. 2006, 42, 1126. [Khim. Geterotsikl. Soedin. 2006, 1302.]

For this article in the English edition see DOI 10.1007/s10593-006-0215-y

 

Downloads

Published

2023-05-18

Issue

No. 9 (2006)

Section

Original Papers