Synthesis, spectroscopic, thermal and antimicrobial studies of some novel metal complexes of Schiff base derived from [N1-(4-methoxy-1,2,5-thiadiazol-3-yl)sulfanilamide] and 2-thiophene carboxaldehyde.
ABSTRACT Keeping in view the chemotherapeutic of the sulfa-drugs, Schiff base namely 2-thiophene carboxaldehyde-sulfametrole (HL) and its tri-positive and di-positive metal complexes have been synthesized and characterized by elemental analyses, IR, 1H NMR, solid reflectance, magnetic moment, molar conductance, mass spectra, UV-vis and thermal analysis (TGA and DrTG). The low molar conductance values suggest the non-electrolytic nature of these complexes. IR spectra show that HL is coordinated to the metal ions in a tetradentate manner through hetero five-membered ring-S and azomethine-N, enolic sulfonamide-OH and thiadiazole-N, respectively. Zn(II), Cd(II) and UO2(II) complexes are found to be diamagnetic (as expected). The proposed general formulae of the prepared complexes are [M2X4(HL)(H2O)4] (where M=Mn(II), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II), X=Cl, [Fe2Cl6(HL)(H2O)2], [(FeSO4)2(HL)(H2O)4] and [(UO2)2(HL) (NO3)4].H2O. The thermal behaviour of these chelates shows that the hydrated complexes loss water of hydration in first step in case of uranium complexes followed loss coordinated water followed immediately by decomposition of the anions and ligand molecules in the subsequent steps. The activation thermodynamic parameters, such as DeltaE*, DeltaH*, DeltaS*, and DeltaG* are calculated from the DrTG curves using Coats-Redfern method. The antimicrobial activity of the obtained products was performed using Chloramphenicol and Grisofluvine as standards, indicate that in some cases metallation increase activity than the ligand.
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ABSTRACT: The title Schiff base compound, C15H17N3O2S, is non-planar with a dihedral angle of 69.88 (4)° between the planes of the benzene rings. In the crystal, pairs of N-H⋯N hydrogen bonds, between the sulfonamide nitro-gen-H atom and the azomethine N atom, link the mol-ecules into inversion dimers, forming R 2 (2)(16) ring motifs. These dimers are linked by N-H⋯O hydrogen bonds, between the sulfonamide nitro-gen-H atom and one sulfonamide O atom, forming sheets lying parallel to (100). Within the sheets there are weak parallel slipped π-π inter-actions involving inversion-related benzene-sulfonamide rings [centroid-centroid distance = 3.8800 (9) Å; normal distance = 3.4796 (6) Å; slippage = 1.717 Å].Acta Crystallographica Section E Structure Reports Online 06/2014; 70(Pt 6):o726-7. · 0.35 Impact Factor
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ABSTRACT: A new series of transition metal complexes of 2,4-bis(indolin-3-one-2-ylimino)-6-phenyl-1,3,5-triazine) (BIPTZ) have been synthesized. The structural features of BIPTZ and metal(II) complexes were investigated using elemental analyses, magnetic susceptibility, molar conductance, mass, IR, UV–Vis, 1H NMR, 13C NMR, CV, and ESR spectral studies. Electronic absorption spectra and magnetic susceptibility measurements of the complexes predict their geometry. The redox behavior of the copper(II) complexes has been studied by cyclic voltammetry. All the synthesized compounds may serve as potential photoactive materials as indicated from their characteristic fluorescence spectrum. The Schiff base and its metal complexes were screened for anticonvulsant and anti-inflammatory activities in vivo. The metal(II) complexes are potent agents in treating neurochemical and behavioral abnormalities seen in Parkinson’s diseased (PD) mice than free ligand.Medicinal Chemistry Research 01/2014; · 1.61 Impact Factor
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ABSTRACT: The azodye ligand (HL(1)) was synthesized from the coupling of sulfaguanidine diazonium salt with 2,4-dihydroxy-benzaldehyde while the two ligands, HL(2) and HL(3), were prepared by the coupling of sulfadiazine diazonium salt with salicylaldehyde (HL(2)) and 2,4-dihydroxy-benzaldehyde (HL(3)). The prepared ligands were characterized by elemental analysis, IR, (1)H NMR and mass spectra. Cu(II), Co(II) and Ni(II) complexes of the prepared ligands have been synthesized and characterized by various spectroscopic techniques like IR, UV-Visible as well as magnetic and thermal (TG and DTA) measurements. It was found that all the ligands behave as a monobasic bidentate which coordinated to the metal center through the azo nitrogen and α-hydroxy oxygen atoms in the case of HL(1) and HL(3). HL(2) coordinated to the metal center through sulfonamide oxygen and pyrimidine nitrogen. The applications of the prepared complexes in the oxidative degradation of indigo carmine dye exhibited good catalytic activity in the presence of H2O2 as an oxidant. The reactions followed first-order kinetics and the rate constants were determined. The degradation reaction involved the catalytic action of the azo-dye complexes toward H2O2 decomposition, which can lead to the generation of HO radicals as a highly efficient oxidant attacking the target dye. The detailed kinetic studies and the mechanism of these catalytic reactions are under consideration in our group.Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy 10/2013; 121C:180-187. · 1.98 Impact Factor