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A vibrational spectroscopic study of transition metal tetracyanonickelate complexes of 2-chloropyridine and 2-bromopyridine.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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  • Sevim Akyüz
  • Meriç Bakiler
  • J. Eric D. Davies
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<mark>Journal publication date</mark>1996
<mark>Journal</mark>Journal of Coordination Chemistry
Issue number1-4
Volume37
Number of pages6
Pages (from-to)1-6
Publication StatusPublished
<mark>Original language</mark>English

Abstract

The FT-IR and Raman spectra of eight new complexes of formula ML2Ni(CN)4 (where M = Mn, Fe, Co, Ni, Cu or Cd and L = 2-chloropyridine; M = Ni or Cd and L = 2-bromopyridine) are reported. The spectroscopic results indicate that the complexes have structures consisting of corrugated polymeric layers of [M-Ni(CN)4]∞ with 2-substituted pyridine molecules bound directly to the metal (M). For a given ligand (2-Clpy or 2-Brpy) the effects of metal-ligand bond formation on the ligand modes are examined. Metal-ligand bond strengths of the halo-derivatives of pyridine (L = 2-Clpy or 2-Brpy), inferred by the effects on frequency shifts of certain ligand modes, have also been compared.