A new tetraoxime ligand, (2E, 3E, 9E, 10E)-1, 4, 8, 11-tetraazacyclotetradecane-2, 3, 9, 10-tetrone tetraoxime has been prepared by the template condensation of 1,3-propanediamine and cyanogen-di-N-oxide, obtained by treating (E, E)-dichloroglyoxime in CH 2 Cl 2 with Na 2 CO 3 at )10°C. The coordination chain polymers {[(pnngH 2 ) 2 Ni] n (5) and [(pncgH 2 ) 2 Cu] n (6)} of two transition metal ions, [Ni(II) and Cu(II)] with the vic-dioxime ligand have been prepared. The oxime ligand acts as a polydentate ligand bending through nitrogen atoms in the presence of a base, as do most of the vic-dioximes. In the complexes, the chloride ions coordinate to the nickel and copper ions. The structures of these novel vic-dioxime compounds are proposed on the basis of the elemental analyses, molar conductance data, i.r., and U.v.)visible are presented. Elemental analyses indicate a ligand metal ratio of 1:1 in the coordination polymers. Conductivity measurements have shown that mono-and polynuclear complexes are non-electrolytes. In addition, anti-microbial activities of the compounds have been investigated.
A novel vic-dioxime ligand containing the thiourea group, (4E,5E)-1,3-bis{4-[(4-methylphenylamino)methyl] phenyl}-2-thiooxaimidazoline-4,5-dione dioxime, (4) mmdH 2 has been prepared from N,N¢-bis{4-[(4-methylphenylamino)methyl]phenyl}thiourea, (3) mft and cyanogen di-N-oxide. Mononuclear [M(mmdH) 2 ], where M=Ni II , Co II and Cu II complexes of the (4) mmdH 2 bidentate ligand have been obtained with a 1:2 metal:ligand ratio, as do most the vic-dioximes. The complexes are formed by coordination of N, N atoms of the ligand. The vic-dioxime ligand and its some transition metal complexes have been characterized by elemental analyses, molar conductance data, magnetic susceptibility, i.r., 1 H-n.m.r and u.v.-vis. spectroscopy. Conductivity measurements have shown that mononuclear complexes are non-electrolytes. In addition, the ligands and metal complexes were screened for antibacterial and antifungal activities by agar well diffusion techniques using DMF as solvent.
A new vicinal dioxime ligand containing azo and thione chromophores, namely 1,3-bis[4-(phenyldiazenyl)-phenyl]-2-thiooxaimidazoline-4,5-dione dioxime (bppH 2 ), was synthesized by the reaction of cyanogen di-N-oxide with N,N 0 -bis(4-phenylazophenyl) thiourea in dichloromethane solution at -10°C. Mononuclear complexes of bppH 2 with nickel(II), cobalt(II), and copper(II) were synthesized. The complexes, [Ni(bppH) 2 ], [Cu(bppH) 2 ], and [Co(bppH) 2 ] were characterized by several techniques using elemental analyses, conductivity measurements, FT-IR, and electronic spectral studies. The data suggest that the ligand coordinates through the N,N atoms, as do most vic-dioximes. The molar conductivities in DMF solution indicate nonelectrolytic nature for the complexes. Antimicrobial activities of the ligand and its metal complexes were estimated for five bacteria, namely Klebsiella pneumoniae, Micrococcus luteus, Mycobacterium smegmatis, Enterobacter cloaca and Bacillus megaterium and three fungi, namely Candida albicans, Kluyveromyces marxianus, and Rhodotorula rubra.
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