Abstract
We have performed theoretical multiconfigurational calculations of the molecular energy levels based on two axial ligand field models and determined the model parameters to reproduce ab initio energies of TiCl(2), TiF(2), VCl(2), and VF(2). We develop two extensions to ligand field theory (LFT) for linear transition metal dihalides, which are incorrectly described by standard LFT. The standard LFT is augmented (1) by including the ligand induced hybridization of the d(sigma) orbital with the 4s orbital or (2) by using a different radial part for the d(sigma) orbital. Both models reproduce the energies of the first electronic states in very good agreement with numerical multireference configuration interaction results. Furthermore the model parameters are very close to experimental known Racah parameters describing the term energies of Ti(2+) and V(2+).
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