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Please use this identifier to cite or link to this item: https://ri.ufs.br/jspui/handle/riufs/24555
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dc.contributor.authorOliveira, Adriano Bof de-
dc.contributor.authorFeitosa, Bárbara Regina Santos-
dc.contributor.authorNäther, Christian-
dc.contributor.authorJess, Inke-
dc.date.accessioned2026-02-09T17:24:05Z-
dc.date.available2026-02-09T17:24:05Z-
dc.date.issued2014-
dc.identifier.citationOLIVEIRA, A. B. et al. N-Phenyl-2 (1,2,3,4-tetrahydronaphthalen-1-ylidene) hydrazinecarbothioamide. Acta Crystallographica Section E, Chester, v. 70, n. 2, 2014. Disponível em: https://journals.iucr.org/e/issues/2014/02/00/bt6959/index.html. Acesso em: 9 fev. 2026.pt_BR
dc.identifier.issn1600-5368-
dc.identifier.urihttps://ri.ufs.br/jspui/handle/riufs/24555-
dc.languageengpt_BR
dc.publisherInternational Union of Crystallographypt_BR
dc.relation.ispartofActa Crystallographica Section Ept_BR
dc.subjectSingle-crystal X-ray studyeng
dc.subjectT = 200 Keng
dc.subjectMean (C–C) = 0.002 A˚eng
dc.subjectR factor = 0.036eng
dc.subjectWR factor = 0.089eng
dc.subjectData-to-parameter ratio = 18.5eng
dc.titleN-Phenyl-2 (1,2,3,4-tetrahydronaphthalen-1-ylidene) hydrazinecarbothioamidept_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.resumoThe conformation of the title molecule, C17H17N3S, is stabilized by an intramolecular N—HN hydrogen bond involving the azometinic group. The dihedral angle between the two aromatic rings is 36.49 (06). The non-aromatic ring of the tetralone substituent adopts a sofa conformation. In the crystal, molecules are linked by pairs of N—HS hydrogen bonds related via centres of symmetry, forming dimers.pt_BR
dc.description.localChesterpt_BR
dc.identifier.doihttps://doi.org/10.1107/S1600536814001585-
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