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dc.contributor.authorSarıkavaklı, N.
dc.contributor.authorBabahan, I.
dc.contributor.authorŞahin, E.
dc.contributor.authorHökelek, T.
dc.date.accessioned2019-12-13T06:25:11Z
dc.date.available2019-12-13T06:25:11Z
dc.date.issued2008
dc.identifier.issn1600-5368
dc.identifier.urihttps://doi.org/10.1107/S1600536808004947
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960784/
dc.identifier.urihttp://hdl.handle.net/11655/18081
dc.description.abstractIn 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 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.
dc.relation.isversionof10.1107/S1600536808004947
dc.rightsinfo:eu-repo/semantics/openAccess
dc.title2-Hydroxy­Imino-1-Phenyl­Ethanone Thio­Semicarbazone Monohydrate
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalActa Crystallographica Section E: Structure Reports Online
dc.contributor.departmentFizik Mühendisliği
dc.identifier.volume64
dc.identifier.issuePt 3
dc.identifier.startpageo623
dc.identifier.endpageo624
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus


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