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dc.contributor.authorAmim, Raquel dos Santos-
dc.contributor.authorOliveira, Marcelo Ribeiro Leite-
dc.contributor.authorPerpétuo, Genivaldo Julio-
dc.contributor.authorJanczak, Jan-
dc.contributor.authorMiranda, Liany Divina Lima-
dc.date.accessioned2015-03-31T20:48:17Z-
dc.date.available2015-03-31T20:48:17Z-
dc.date.issued2008-
dc.identifier.citationAMIM, R. dos S. et al. Syntheses, crystal structure and spectroscopic characterization of new platinum(II) dithiocarbimato complexes. Polyhedron, v. 27, p. 1891-1897, 2008. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0277538708001149>. Acessoe em: 20 fev. 2015.pt_BR
dc.identifier.issn0277-5387-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/4830-
dc.description.abstractThe reaction of 4-iodobenzenesulfonamide or 4-fluorobenzenesulfonamide with CS2 and KOH in dimethylformamide yielded the potassium N-R-sulfonyldithiocarbimates, K2(RSO2N@CS2) [R = 4-IC6H4 (1) and 4-FC6H4 (2)]. These salts reacted with K2[PtCl4] in water/methanol to yield complex anions bis(N-R-sulfonyldithiocarbimato) platinate(II), which were isolated as their tetrabutylammonium salts, (Bu4N)2[Pt(RSO2N@CS2)2] [R = 4-IC6H4 (3) and 4-FC6H4 (4)]. The structures of 2–4 were determined by X-ray crystallography. The Pt2+ in both complexes 3 and 4 lies at the inversion centre and the PtS4 moiety has a distorted square-planar configuration. The compounds were also characterized by IR, 1H NMR and 13C NMR spectroscopies, and elemental analyses. The molar conductance data are consistent with the fact that 3 and 4 are dianionic complexes.pt_BR
dc.language.isoen_USpt_BR
dc.subjectDithiocarbimatespt_BR
dc.subjectPlatinum complexespt_BR
dc.subjectCrystal structurespt_BR
dc.titleSyntheses, crystal structure and spectroscopic characterization of new platinum(II) dithiocarbimato complexes.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.rights.licenseO periódico Polyhedron concede permissão para depósito do artigo no Repositório Institucional da UFOP. Número da licença: 3564801410644.pt_BR
dc.identifier.doihttps://doi.org/10.1016/j.poly.2008.02.030-
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