Journal of the Chemical Society A Inorganic Physical Theoretical · 1971 · 27 citations · 0 references
Natural SciencesChemistryPhysicsCondensed Matter PhysicsSolid State PhysicsSpectroscopyCoordination ChemistryCrystal ChemistryMagnetic Properties Of SolidsMagnetism Of Inorganic CompoundsTransition Metal ChemistryTransition Metal ComplexesCircular DichroismElectronic Spectra Of Transition Metal ComplexesMagnetic Circular DichroismMagnetic Properties Of Transition Metal ComplexesMagnetism Of Transition Metal ComplexesSpectroscopy Of Transition Metal ComplexesSpin-orbit SplittingTemperature Dependence
The magnetic circular dichroism (m.c.d.) spectrum of a single crystal of cubic [Ni(H2O)6](BrO3)2 has been measured at 4 K, and at six temperatures between 77 and 300 K. The m.c.d. parameters for each spin–orbit component of the vibronic d–d bands of the nickel(II) hexaquo-ion have been calculated. The m.c.d. spectrum at 4 K is dominated by C terms arising through both first- and second-order spin–orbit coupling. The signs of the C terms confirm that the dominant active vibration is of t1u symmetry. The quantitative values of C/D, where D is the dipole strength, are determined from a 1/T plot for the ‘red’ band. A comparison with calculated parameters supports the view that the 1aE state is interacting with the 3T1g state leading to the characteristic double-peaked ‘red’ band of the [Ni(H2O)6]2+ spectrum. A pronounced vibrational progression is found in the ‘red’ band at 4 K. The frequencies in the progression can be understood in terms of an interaction between the E spin–orbit components of the 3T1g state and the 1aE(t2g6eg2) state.