The Vibrational Spectra of the Cyanide Ligand Revisited. Double Bridging Cyanides

The ν(CN) vibrational spectra of cyanide groups bridging two metal atoms present a confused picture. Factors relevant to the interpretation of the available data are reviewed. Some mechanisms for frequency change, relative to the corresponding terminal species, are made more quantitative than previously described, and others are highlighted for the first time. The kinematic effect is much less important than previously assumed. It seems that an effect responsible for the major part of the frequency increase upon bridging commonly observed is the cation electric field, together with concomitant relaxation (the IVSE model). However, a contribution may well come from the change in the σ bonding in the CN unit.