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Please use this identifier to cite or link to this item: https://ri.ufs.br/jspui/handle/riufs/24730
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dc.contributor.authorOliveira, Adriano Bof de-
dc.contributor.authorBeck, Johannes-
dc.contributor.authorLandvogt, Christian-
dc.contributor.authorFeitosa, Bárbara Regina Santos-
dc.date.accessioned2026-03-10T18:50:50Z-
dc.date.available2026-03-10T18:50:50Z-
dc.date.issued2015-
dc.identifier.citationOLIVEIRA, A. B. et al. Crystal structure of 4-hydroxy-3-methoxybenzaldehyde 4-methylthiosemicarbazone methanol monosolvate. Acta Crystallographica Section E, Chester, v. 71, n. 5, 2015. Disponível em: https://journals.iucr.org/e/issues/2015/05/00/hb7402/index.html. Acesso em: 10 mar. 2026.pt_BR
dc.identifier.issn2056-9890-
dc.identifier.urihttps://ri.ufs.br/jspui/handle/riufs/24730-
dc.languageengpt_BR
dc.publisherInternational Union of Crystallographypt_BR
dc.relation.ispartofActa Crystallographica Section Ept_BR
dc.subjectCrystal structurepor
dc.subjectBifurcated hydrogen bondpor
dc.subjectThiosemicarbazone derivative from natural productpor
dc.subjectVanillinpor
dc.titleCrystal structure of 4-hydroxy-3-methoxybenzaldehyde 4-methylthiosemicarbazone methanol monosolvatept_BR
dc.typeArtigopt_BR
dc.identifier.licenseCreative Commons Atribuição 2.0 Reino unido: Inglaterra e País de Gales (CC BY 2.0 UK)pt_BR
dc.description.resumoIn the title solvate, C15H15N3O2SCH3OH, the thiosemicarbazone molecule is approximately planar; the maximum deviation from the mean plane is 0.4659 (14) A˚ and the dihedral angle between the aromatic rings is 9.83 (8). This conformation is supported by an intramolecular N— HN hydrogen bond. In the crystal, the thiosemicarbazone molecules are linked into dimers by pairs of N—HS hydrogen bonds, thereby generating R2 2 (8) loops. The methanol solvent molecule bonds to the thiosemicarbazone molecule through a bifurcated O—H(O,O) hydrogen bond and also accepts an O—HO link from the thiosemicarbazone molecule. Together, these links generate a three-dimensional network.pt_BR
dc.description.localChesterpt_BR
dc.identifier.doihttps://doi.org/10.1107/S2056989015007227-
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