Acta Crystallographica Section E (Mar 2008)

2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate

  • Tuncer Hökelek,
  • Ertan Şahin,
  • knur Babahan,
  • Nursabah Sarıkavaklı

DOI
https://doi.org/10.1107/S1600536808004947
Journal volume & issue
Vol. 64, no. 3
pp. o623 – o624

Abstract

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In the title thiosemicarbazone derivative, C9H10N4OS·H2O, intramolecular N—H...N hydrogen bonds result in the formation of two nearly coplanar five- and six-membered rings, which are also almost coplanar with the adjacent phenyl ring. The oxime group has an E configuration and is involved in intermolecular O—H...O hydrogen bonding as a donor. In the crystal structure, intramolecular O—H...S and N—H...N and intermolecular O—H...O and N—H...S hydrogen bonds generate edge-fused R22(8) and R41(11) ring motifs. The hydrogen-bonded motifs are linked to each other to form a three-dimensional supramolecular network.