A water-soluble multisite ionophore ligand bearing pyridine and aminothiophenol functionality. Synthesis, spectroscopy and electrochemistry of its complexes, and peripheral reactivity of the (E,E)M (M = Ni) complex with Pd2+ and Ag+

Kandaz M., Ozkaya A. R., Koca A.

TRANSITION METAL CHEMISTRY, cilt.29, sa.8, ss.847-854, 2004 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 29 Sayı: 8
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1007/s11243-004-1567-8
  • Dergi Adı: TRANSITION METAL CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.847-854
  • Marmara Üniversitesi Adresli: Evet

Özet

The design, synthesis and coordination of a novel multisite vic-dioxime compound, LH2 containing flexible pyridine substituents and amitiophcnylsulfanyl moieties on the periphery, facilitating solubility in water as pyridinium hydrochloride salt are described. LH2 was prepared by the reaction between 2-(2-pyridylethylamino)-benzenethiol and (E,E)-dichloroglydioxime. Mononuclear [(E,E)M] (M = Ni-II, Cu-II. Co-II, Fe-II and Mn-II) and dinuclear uranyl (UO2II) complexes of LH2 were isolated and characterized with metal:ligand ratios of 1:2 and 2:2. respectively. The reaction of Na2PdCl4 . 3H(2)O and AgNo3 in DMF with the mononuclear complex, (LH)(2)Ni, resulted in the formation of the heterotrinuclear complexes [Pd2Ni(LH)(2)]Cl-4 and [Ag2Ni(LH)(2)](NO3)(2). The complexes were characterized by elemental analysis, H-1-n.m.r., u.v.-vis. spectroscopy, i.r., and MS (LSIMS). The redox properties of the complexes were studied by cyclic voltammetry.