Magnetic circular dichroism spectra of some nickel(II) complexes. Part II. Magnetic circular dichroism of d–d transitions in octahedral nickel(II) complexes in solution
Abstract
The magnetic circular dichroism spectra of the complexes [NiL6]2+(L = H2O, NH3, or dimethyl sulphoxide) and [NiL′3]2+(L′= ethylenediamine or 2,2′-bipyridyl) have been measured in solution at room temperature. All the spectra are dominated by B and C terms which arise respectively from the second-order Zeeman effect and spin–orbit coupling interactions between the 3A2g ground state and 3T2g excited state. No A terms are observed and in most cases first-order C terms associated with the different spin–orbit components of the particular transition are swamped. Pronounced vibrational structure is observed when the 1aE state is close to the 3T2g state.