Abstract
The structures and some vertical excitation energies of third-row transition metal hexafluorides (MF6, M = Re, Os, Ir, Pt, Au, Hg) were calculated using the multi-reference configuration interaction (MRCI) theory based on exact two-component (X2C) Hamiltonian. The spin-orbit coupling (SOC) was variationally included at the Hartree-Fock level, enabling us to analyze the SOC at the orbital level. The excitation spectra were assigned based on the double group, a relativistic group theory applicable to states with the SOC. This study provides a fundamental understanding of the ligand field splitting, including the SOC, that is useful for the photochemistry and spin chemistry involving heavy elements.
Supplementary materials
Title
Supporting information
Description
Details of the optimization and the schematic orbital energy diagrams, including the AuF6 molecule.
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