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URI permanente para esta coleçãohttps://locus.ufv.br/handle/123456789/11800

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    Avaliação de bis(4-metilfenilditiocarbimato)zincato(II) de tetrabutilamônio como acelerador em composições de borracha natural
    (Polímeros, 2008) Mariano, Roberta M.; Visconte, Leila L. Y.; Oliveira, Marcelo R. L.; Rubinger, Mayura M. M.
    Neste trabalho a substância ZNIBU [bis(4-metilfenilditiocarbimato)zincato(II) de tetrabutilamônio] foi usada em formulações de borracha natural (NR) e o seu efeito como acelerador de vulcanização foi investigado. As composições, vulcanizadas com a substância em questão, foram submetidas a testes mecânicos e os resultados comparados com os de outras composições vulcanizadas com os aceleradores comerciais CBS (N-ciclohexil-2-benzotiazol-2-sulfenamida), TMTD (dissulfeto de tetrametiltiuram) e MBTS (dissulfeto de benzotiazol). Propriedades como dureza, resiliência e densidade foram avaliadas em presença ou não da carga negro de fumo.
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    Synthesis, structural and spectroscopic characterization of novel zinc(II) complexes with N-methylsulfonyldithiocarbimato and N-methylsulfonyltrithiocarbimato ligands
    (Polyhedron, 2007-01-02) Oliveira, Marcelo R. L.; Perpetuo, Genivaldo J.; Janczak, Jan; Rubinger, Mayura M. M.
    Two new zinc(II)-complexes, dithiocarbimato (Ph4P)2[Zn(CH3SO2N=CS2)2] (1) and trithiocarbimato (Ph4P)2[Zn(CH3SO2N=CS3)2] (2), were obtained in the crystalline form by the reaction of potassium N-methylsulfonyldithiocarbimate (RSO2N=CS2K2) with zinc(II) acetate dihydrate and tetraphenylphosphonium chloride in dimethylformamide. Both complexes crystallize in the monoclinic system. The central Zn(II) ion has a distorted tetrahedral coordination in both compounds. In 1 the dithiocarbimato ligand coordinates via two S atoms while in 2 the trithiocarbimato ligand coordinates via S and N atoms. Both complexes were also characterized by IR, 1 H NMR and 13C NMR spectroscopies. Compound 2 is the first example of a zinc(II)-trithiocarbimato complex.
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    Preparation, crystal structure and spectroscopic characterization of nickel(II) complexes with dithiocarbimate derivated of sulfonamides
    (Polyhedron, 2006-07-10) Oliveira, Marcelo R. L.; Franca, Eduardo de Faria; Guilardi, Silvana; Andrade, Renato Pereira de; Lindemann, Renata Hernandez; Amim Jr., Jorge; Ellena, Javier; Bellis, Vito M. de; Rubinger, Mayura M. M.
    This work describes the syntheses of three compounds containing [Ni(RSO2N=CS2)2]^2 anions: (Bu4N)2[Ni(CH3CH2SO2N=CS2)2] (1), (Bu4N)2[Ni(4-IC6H4SO2N=CS2)2] (2) and (Bu4N)2[Ni(2,5-Cl2C6H3SO2N=CS2)2] (3). They were obtained in the crystalline form by the reaction of the appropriate potassium N-R-sulfonyldithiocarbimate (RSO2N=CS2K2) with nickel(II) chloride hexahydrate in methanol/water. Elemental analyses were consistent with the proposed formulae. UV–Vis and IR data are consistent with the formation of nickel–sulfur diamagnetic planar complexes. The 1H NMR and 13C NMR spectra showed the expected signals for the tetrabutylammonium cation and the dithiocarbimate moieties. Single crystal structure analyses showed that 1 crystallizes in the monoclinic space group P21/n, 2 crystallizes in the monoclinic space group P21/c and 3 crystallizes in the triclinic space group Pī. In these compounds the Ni. atom is coordinated to four S atoms in a distorted square plane geometry due to the asymmetric bidentade chelation by each ligand.
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    Syntheses, crystal structure, spectroscopic characterization and antifungal activity of new N-R-sulfonyldithiocarbimate metal complexes
    (Journal of Inorganic Biochemistry, 2009-07) Alves, Leandro C.; Rubinger, Mayura M. M.; Lindemann, Renata H.; Perpétuo, Genivaldo Júlio; Janczak, Jan; Miranda, Liany D. L.; Zambolim, Laércio; Oliveira, Marcelo R. L.
    Five new compounds with the general formula of (Bu4N)2[M(RSO2NCS2)2], where Bu4N = tetrabutylammonium cation, (M = Ni, R = 4-FC6H4) (1), (M = Zn, R = 4-FC6H4, 4-ClC6H4, 4-BrC6H4, 4-IC6H4), (2), (3), (4) and (5), respectively, were obtained by the reaction of the appropriate potassium N-R-sulfonyldithiocarbimate (RSO2NCS2K2) with nickel(II) chloride hexahydrate or zinc(II) acetate dihydrate in metanol:water 1:1. The elemental analyses and the IR data are consistent with the formation of the expected bis(dithiocarbimato)metal(II) complexes. The 1H and 13C NMR spectra showed the signals for the tetrabutylammonium cation and the dithiocarbimate moieties. The compounds 1, 2 and 5 were also characterized by X-ray diffraction techniques. The nickel(II) is coordinated by two N-4-fluorophenylsulphonyldithiocarbimato(2-) ligands forming a planar coordination. The zinc(II) exhibits distorted tetrahedral configuration in compounds 2 and 5 due to the chelation effect of two sulfur atoms of the N-R-sulfonyldithiocarbimate ligands. The antifungal activities of the compounds were tested in vitro against Colletotrichum gloeosporioides, an important fungus that causes the plant disease known as anthracnose in fruit trees. All the complexes were active.
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    Syntheses, characterization and antifungal activity of tris(1,10-phenanthroline)iron(ii) bis(n-r-sulfonyldithiocarbimate)zincate(ii)
    (Química Nova, 2013-05-25) Bottega, Fernanda C.; Oliveira, Marcelo R. L.; Garcia, Camila V.; Menezes, Daniele C.; Rubinger, Mayura M. M.; Zambolim, Laercio
    Four new compounds with the general formula [Fe(phen)3][Zn(RSO2N=CS2)2], where phen = 1,10-phenanthroline, R = 4-FC6H4 (1), 4-ClC6H4 (2), 4-BrC6H4 (3) and 4-IC6H4 (4), respectively, were obtained by the reaction of the appropriate potassium N-R-sulfonyldithiocarbimate (RSO2N=CS2K2) and tris(1,10-phenanthroline)iron(II) sulfate, with zinc(II) acetate dihydrate in dimethylformamide. The elemental analyses and the IR data were consistent with the formation of the expected complexes salts. The 1H and 13C NMR spectra showed the signals for the cationic iron(II) complex and dithiocarbimate moieties. The molar conductance data were consistent with the 1:1 cation:anion complexes in 1-4. The antifungal activities of the compounds were tested in vitro against Candida albicans, Candida tropicalis and Colletotrichum gloeosporioides.