Two Crystal Modifications of the Cocrystal of 5-(hydroxyimino)-1H-Imidazole-3-Oxide with 3,4-Diaminoglyoxime

Two crystal modifications of the cocrystal of (Z)-4-amino-5-(hydroxyimino)-2,2-dimethyl-2,5-dihydro-1H-imidazole-3-oxide with 3,4-diaminoglyoxime in the 2:1 stoichiometric component ratio are studied by single-crystal XRD. It is established molecules of both modifications demonstrate highly similar geometric parameters. Noncovalent bonding in the crystals of both forms is analyzed comprehensively by constructing Hirshfeld surfaces. It is shown that 1H-imidazole-3-oxide chains are rearranged, the fraction of N–H⋯N interactions is diminished and their character is changed upon the introduction of a water molecule into the structure of one modification, while its calculated density and the coefficient of molecular packing in the crystal are not changed significantly.

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Publication Details

Journal
Journal of Structural Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1134/s0022476625120091
Primary Topic
Synthesis and Reactions of Organic Compounds
Type
article
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article

Two Crystal Modifications of the Cocrystal of 5-(hydroxyimino)-1H-Imidazole-3-Oxide with 3,4-Diaminoglyoxime

V. M. Pronina, F. I. Guseinov, E. V. Shuvalova, K. A. Afanaseva et al.
Journal of Structural Chemistry
Synthesis and Reactions of Organic Compounds
article

Two Crystal Modifications of the Cocrystal of 5-(hydroxyimino)-1H-Imidazole-3-Oxide with 3,4-Diaminoglyoxime

V. M. Pronina, F. I. Guseinov, E. V. Shuvalova, K. A. Afanaseva, A. I. Samigullina, A. V. Stepanov, L. M. Glukhov
article en

Abstract

Two crystal modifications of the cocrystal of (Z)-4-amino-5-(hydroxyimino)-2,2-dimethyl-2,5-dihydro-1H-imidazole-3-oxide with 3,4-diaminoglyoxime in the 2:1 stoichiometric component ratio are studied by single-crystal XRD. It is established molecules of both modifications demonstrate highly similar geometric parameters. Noncovalent bonding in the crystals of both forms is analyzed comprehensively by constructing Hirshfeld surfaces. It is shown that 1H-imidazole-3-oxide chains are rearranged, the fraction of N–H⋯N interactions is diminished and their character is changed upon the introduction of a water molecule into the structure of one modification, while its calculated density and the coefficient of molecular packing in the crystal are not changed significantly.

Journal of Structural ChemistryVol. 66(12)
A. N. Kosygin Moscow State Textile University (RU), N.D. Zelinsky Institute of Organic Chemistry (RU)
Openalex Percentile: Top 32%
Synthesis and Reactions of Organic Compounds
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