The mixing of one mole of 2,2'-bipyridine-3,3'-dicarboxylic acid (bpdc) with two mole of potassium hydroxide (KOH) in methanol were refluxed for (half hour), followed by addition of one mole methanol solution of MCl2.nH2O (where M=Co, Ni or Cu). The mixture was refluxed for (2 hours) to give colored complexes of the metal ions of [M(bpdc)(H2O)4]. The [M(bpdc)(H2O)4] were reacted with one mole of 2-Mercapto-5-phenyl-1,3,4-oxadiazole (phozSH) producing the colored mixed ligand complexes with general formula [M(bpdc)(phozSH)(H2O)3] in which the metal ions coordinated to the ligand through O-atoms of carboxyl group in (bpdc) and N-atom of (phozSH) ligand. The ligands and complexes are well identified by using Furrier transform infrared spectroscopy, 1H-NMR, 13C-NMR, Electronic spectroscopy, CHNS analysis, Melting point, conductivity measurement. The Antioxidant activity were screened for all the complexes by the use of 2, 2-diphenyl-1-picrylhydrazyl (DPPH) method.
ABSTRACT-dppmCl)Cl 2 ] complexes and then add the ligand HSBIBT to these complexes to form mixed ligand complexes. The prepared complexes have been characterized by single-crystal X-ray diffraction, elemental analysis, magnetic susceptibility, molar conductance, IR spectral data and UV-Visible. The results suggested that the ligand HSBIBT bonded to the metal through N atom and square planner geometries were assigned for the complexes.
Treatment of 2-Mercaptobenzimidazol (HL) with the mercuric acetate (Hg(OAc) 2) give the complex[Hg(L) 2 ] (1). Then the multinuclear complexes of the type [M 2 Hg 2 (L) 4 Cl 4 ] were prepared through the reaction of complex (1) with each of NiCl 2 .6H 2 O, PdCl 2 and PtCl 2 in (2:2) molar ratio. All complexes were described using infrared spectra, Proton Nuclear Magnetic Resonance , Carbon 13-Nuclear Magnetic Resonance , ultraviolet-visible, atomic absorption spectroscopy, CHNS analysis, molar conductivity, determination of Chloride Percentage and magnetic susceptibility measurements.The heterocyclic ligand is expected to be coordinated to two or single metal atom through the nitrogen atom and sulphur atom or by only sulphur atom.
Platinum(II) complex consisting of the tertiarydiphosphine (dppm) ligand had been prepared from PdCl2 with one equiv. of dppm ligand to form [PtC2(dppmCl)] complex where as dppmCl is bis(dipheny1phosphino) chloromethene. Crystal was grown in dichloromethane by slow evaporation process and characterized by X-ray crystallography technic. The complex structure synthesized based upon the identification using X-ray Crystallography and FTIR was [PtC12(dppmCl)], the ligand dppm coordinated to the meta centre as bidentate chelating ligand and form square planar arrangement around Pt(II) metal centre. The bond distances of Pt-P1, Pt-P2, Pt- Cl1 and Pt-Cl2 are 2.217 (2), 2.217 (2), 2.3661 (19) and 2.3661 Aο respectively. The characterized results of Pt(II) complex using X-ray analysis illustrated that [PtC12(dppmCl)] Complex form monoclinic crystal with unit cell dimensions of a = 16.2034(5), b = 7.8274(2), and c = 19.2496 (6) Aο, with β = 98.918 (1)ο, Z=4, calculated density= 1.838 mg/m3, T= 200 k and space group C2/c
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