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    Synthesis, X-ray structure and study of a mixed ligand iron(III) complex with tridentate Schiff base as a homogeneous catalyst in the efficient oxidation of sulfides

    , Article Inorganic Chemistry Communications ; Volume 12, Issue 6 , 2009 , Pages 476-480 ; 13877003 (ISSN) Bagherzadeh, M ; Tahsini, L ; Latifi, R ; Amani, V ; Ellern, A ; Keith Woo, L ; Sharif University of Technology
    2009
    Abstract
    A mononuclear mixed ligand complex of iron, [FeIII(N-OPh-sal)(acac)EtOH], where Hacac and N-HOPh-Hsal denote acetylacetone and N-hydroxyphenyl-salicylideneamine, respectively, has been synthesized and characterized by elemental analysis, spectral studies and X-ray crystallography. The catalytic system containing this complex and urea hydrogen peroxide as oxidizing agent was used to selectively oxidize a range of sulfides to the corresponding sulfoxides in good yields under mild conditions. The electronic spectra of the catalytic system were applied to explore reactivity and stability of the catalyst during sulfide oxidation reactions and to examine the nature of active species, as well. ©... 

    Synthesis, characterization and fluorescence spectra of mixed ligand Zn(II), Cd(II) and Hg(II) complexes with 1,10-phenanthroline-5,6-dione ligand

    , Article Journal of Coordination Chemistry ; Volume 60, Issue 15 , 2007 , Pages 1629-1635 ; 00958972 (ISSN) Boghaei, D. M ; Behzadian Asl , F ; Sharif University of Technology
    2007
    Abstract
    The novel mixed ligand complexes [M(bpy)(phen-dione)](PF6)2 (M = Zn(II), Cd(II) and Hg(II), bpy = 2,2′-bipyridine and phen-dione = 1,10-phenanthroline-5,6-dione) have been synthesized and characterized by elemental analysis, IR, 1H NMR and electronic absorption spectroscopies. The ν(C=O) of coordinated phen-dione in these complexes are very similar to the free phen-dione ligand showing that phen-dione is not coordinated to metal ion from its C=O sites. Absorption spectra of the complexes show two absorption bands for intraligand transitions. These absorption bands show dependence to the dielectric constant of solvent. These complexes exhibit an intensive fluorescence band around 535 nm in... 

    Stability of binary and ternary copper (II) complexes of 2((4-methyl-5-nitro-6-(pyrrolidine-l-yl)pyrimidine-2-yl) amino) propionic acid in aqueous solution

    , Article Scientia Iranica ; Vol. 21, Issue. 6 , 2014 , pp. 2029-2035 ; ISSN: 10263098 Sajadi, S. A. A ; Bagherzadeh, G ; Khaleghian, M ; Kermani, M ; Sharif University of Technology
    Abstract
    The acidity and stability constants of M (MNPPAP) (MNPPAP: 2((4-methyl-5-nitro-6-(pyrrolidine-l-yl)pyrimidine-2-yl)amino)propionic acid) M: Cu2+, Cu (Bpy)2+ (Bpy: 2,2'-Bipyridine), or Cu(Phen) (Phen: 1,10-Phenanthroline) complexes were determined by potentiometric pH titration. It is shown that the stability of the binary Cu (MNPPAP) complex is determined by the basicity of the carboxylate group on one side and amine group on the other side. It is demonstrated that the equilibrium, Cu(Har)2+ (H ar: Heteroaromatic ligand such as Bpy or Phen) + Cu(MNPPAP) ^ Cu(Har)(MNPPAP) + Cu2+, is displacement due to the well known experience that mixed ligand complexes formed by a divalent 3d ion, a...