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2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate
In the title thiosemicarbazone derivative, C(9)H(10)N(4)OS·H(2)O, 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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960784/ https://www.ncbi.nlm.nih.gov/pubmed/21201956 http://dx.doi.org/10.1107/S1600536808004947 |
Sumario: | In the title thiosemicarbazone derivative, C(9)H(10)N(4)OS·H(2)O, 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 R (2) (2)(8) and R (4) (1)(11) ring motifs. The hydrogen-bonded motifs are linked to each other to form a three-dimensional supramolecular network. |
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