Abstract
The infrared spectra, in
the region 1600-200 cm-1, of a series of complexes formed by
transition metal halides with substituted pyridines have been recorded. The
assignment of the vibrational bands of the ligands and their shifts in
frequency on coordination with a metal ion are discussed. A study of the
metal-nitrogen stretching frequencies of tetrahedral complexes of the type, MX2
L2, where the metal is cobalt or zinc, shows that no simple
relationship exists between the magnitude of these frequencies and the nature
of either the metal ion or the substituted pyridine ligand.
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