Structural, spectroscopic characterization and EPR spectra of nitrato-μ-[N,N'-ethylenebis(3-methoxysalicylideneimine) Cu(II)Ag(I)] complex.

A novel heterodinuclear complex formed by the reaction of silver nitrate with Schiff base complex of copper(II) has been synthesized and characterized by Infrared (IR), ultraviolet-visible (UV-VIS), electron paramagnetic resonance (EPR) and X-ray diffraction methods. Preparation and crystal structure of the heterodinuclear complex, LCuAgNO3, (L=N,N'-ethylenebis(3-methoxysalicylideneimine) are reported. The crystal structure consists of ordered dinuclear units with CuII and AgI ions are bridged by two oxygen atoms of Schiff base ligand.

Synthesis, crystal structure, EPR spectra of Cu2+ doped [Zn(methylisonicotinate)2(H2O)4]·(sac)2 single crystal.

The tetraaquabis(methylisonicotinate)zinc(II) disaccharinate [hereafter, [Zn(mein)2(H2O)4]·(sac)2], complex has been synthesized and characterized by spectroscopic IR, EPR and X-ray diffraction technique. The octahedral Zn(II) ion, which rides on a crystallographic centre of symmetry, is coordinated by two monodentate mein ligands through the ring nitrogen and four aqua ligands to form discrete [Zn(mein)2(H2O)4] unit, which captures two saccharinate ions in up and down positions, each through intermolecular hydrogen bonds. The magnetic environments of Cu2+ doped [Zn(mein)2(H2O)4]·(sac)2 complex have been identified by electron paramagnetic resonance (EPR) technique.

An EPR study of Cu2+ doped diaquabis(nicotinamide)bis(o-sulfobenzimidato-N)-cadmium(II) single crystals.

The electron paramagnetic resonance spectra of Cu(2+) doped diaquabis(nicotinamide)bis(o-sulfobenzimidato-N)-cadmium(II) (hereafter, CdNAS) single crystals which were taken at room temperature are discussed. It was found from the analysis of the EPR data that the Cu(2+) ions substitute for magnetically inequivalent Cd(2+) ions. Two magnetically inequivalent Cu(2+)sites were observed.

EPR studies of VO2+ doped bis(saccharinato)bis(pyridine) zinc (II) single crystals.

Electron paramagnetic resonance (EPR) studies of vanadyl ions, VO2+, as paramagnetic impurity in bis(saccharinato)bis(pyridine)zinc (II) [hereafter, Zn(sac)2(py)2] are made at room temperature. The angular variation of the EPR spectra has shown that three different VO2+ complexes are located in different chemical environments and each environment contains two magnetically inequivalent VO2+ sites in distinct orientations occupying substitutional positions in the lattice and show very high angular dependence. The spin-Hamiltonian parameters are determined and these parameters have been used to assess the bonding coefficients of the VO2+ ion in [Zn(sac)2(py)2] lattice.

Structural characterization and EPR spectral studies on mononuclear copper(II) complex of saccharin with ethylnicotinate.

Mononuclear copper(II) saccharinate (sac) complex containing ethylnicotinate (enc), [Cu(enc)(2)(sac)(2)(H(2)O)].1.4H(2)O has been synthesized and characterized by spectroscopic (IR, UV-vis, EPR), X-ray diffraction technique and electrochemical methods.

EPR study of Cu(2+)-doped tetraaqua-di(nicotinamide)Co(II) saccharinate single crystals.

The electron paramagnetic resonance spectra of Cu(2+) impurities in [Co(nicotinamide)(2)(H(2)O)(4)](saccharinate)(2) single crystals have been studied at ambient temperature in three mutually perpendicular planes. The angular variation of the spectra shows that the Cu(2+) ion substitutes the Co(2+) site in the lattice. The EPR spectra of Cu(2+) ions are characteristic of tetragonally elongated octahedral site.