Article ID Journal Published Year Pages File Type
9757030 Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2005 9 Pages PDF
Abstract
Novel hexachlorocyclodiphosph(V)azane of sulfaguanidine, H4L, l,3-[N′-amidino-sulfanilamide]-2,2,2,4,4,4-hexachlorocyclodiphosph(V)azane was prepared and its coordination behaviour towards the transition metal ions Fe(III), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and UO2(II) was studied. The structures of the isolated products are proposed based on elemental analyses, IR, UV-vis, 1H NMR, mass spectra, reflectance, magnetic susceptibility measurements and thermogravimetric analysis (TGA). The hyperfine interactions in the isolated complex compounds were studied using 14.4 keV γ-ray from radioactive 57Co (Mössbauer spectroscopy). The data show that the ligand are coordinated to the metal ions via the sulfonamide O and deprotonated NH atoms in an octahedral manner. The H4L ligand forms complexes of the general formulae [(MXz)2(H2L)H2O)n] and [(FeSO4)2 (H4L) (H2O)4], where X = NO3 in case of UO2(II) and Cl in case of Fe(III), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II). The molar conductance data show that the complexes are non-electrolytes. The thermal behaviour of the complexes was studied and different thermodynamic parameters were calculated using Coats-Redfern method. Most of the prepared complexes showed high bactericidal activity and some of the complexes show more activity compared with the ligand and standards.
Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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