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dc.contributor.authorFelix, Marcela Campanha-
dc.contributor.authorPerpétuo, Genivaldo Julio-
dc.contributor.authorJanczak, Jan-
dc.date.accessioned2019-06-07T14:33:12Z-
dc.date.available2019-06-07T14:33:12Z-
dc.date.issued2018-
dc.identifier.citationFELIX, M. C.; PERPÉTUO, G. J.; JANCZAK, J. Structural and spectroscopic characterization of bis[1- (diaminomethylene)thiouron-1-ium] naphthalene-1,5-disulfonate. Journal of Molecular Structure, v. 1171, p. 411-419, 2018. Disponível em: <https://www.sciencedirect.com/science/article/pii/S0022286018307348>. Acesso em: 19 mar. 2019.pt_BR
dc.identifier.issn0022-2860-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/11475-
dc.description.abstractSingle crystals of bis[1-(diaminomethylene)thiouron-1-ium] naphthalene-1,5-disulfonate (1) are grown using growth solution technique. The compound crystallizes in the centrosymmetric C2/c space group of the monoclinic system with four molecules per unit cell. The arrangement of oppositely charged units, i.e. 1-(diaminomethylene)thiouron-1-ium cations and naphthalene-1,5-disulfonate anions in the crystal is mainly determined by the ionic and the NeH/O hydrogen bonding interactions. Hirshfeld surface and the analysis of 2D fingerprint plots are illustrating both qualitatively and quantitatively interactions governing the supramolecular arrangement. The compound was also characterized by FT-IR and Raman spectroscopies. The vibrational assignment of the characteristic bands of the functional groups have been supported by the isotopic frequency shift.pt_BR
dc.language.isoen_USpt_BR
dc.rightsrestritopt_BR
dc.subjectCrystal structurept_BR
dc.subjectHydrogen bondpt_BR
dc.subjectHirshfeld surfacept_BR
dc.subjectVibrational spectroscopypt_BR
dc.titleStructural and spectroscopic characterization of bis[1- (diaminomethylene)thiouron-1-ium] naphthalene-1,5-disulfonate.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.identifier.uri2https://www.sciencedirect.com/science/article/pii/S0022286018307348pt_BR
dc.identifier.doihttps://doi.org/10.1016/j.molstruc.2018.06.033pt_BR
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