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


Bozkurt E., Doner A., Ucar I., Karabulut B.

SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, vol.79, no.5, pp.1829-1836, 2011 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 79 Issue: 5
  • Publication Date: 2011
  • Doi Number: 10.1016/j.saa.2011.05.067
  • Journal Name: SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1829-1836
  • Keywords: X-ray diffraction, IR, Crystal structure, EPR, Cu2+ ion, Spin-Hamiltonian, ELECTRON-PARAMAGNETIC-RESONANCE, SACCHARINATE, COMPLEXES, VO2+, DIFFRACTION, HYDRATE, CU-2+, IONS, NI, CO
  • Ondokuz Mayıs University Affiliated: Yes

Abstract

The tetraaquabis(methylisonicotinate)zinc(II) disaccharinate thereafter, [Zn(mein)(2)(H2O)(4)]center dot(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)]center dot(sac)(2) complex have been identified by electron paramagnetic resonance (EPR) technique. EPR spectra of Cu2+ doped [Zn(mein)(2)(H2O)(4)]center dot(sac)(2) single crystals have been studied between 113 and 300 K in three mutually perpendicular planes. The calculated results of the Cu2+ doped [Zn(mein)(2)(H2O)4]center dot(sac)(2) indicate that Cu2+ ion contains two different complexes and each complexes are located in different chemical environments and each environment contains two magnetically inequivalent Cu2+ sites in distinct orientations occupying substitutional positions in the lattice. The vibrational spectra of this compound were discussed in relation to other compounds containing methyl isonicotinate and saccharinate complexes. The assignments of the observed bands were discussed. (C) 2011 Elsevier B.V. All rights reserved.