A consequence of Crystal Field Theory is that the distribution of electrons in the orbitals can lead to stabilisation for some electron configurations. It is a simple matter to calculate the stabilization since all that is needed is the electron configuration. For an octahedral complex, an electron in the more stable t2(g) subset is treated as contributing −25Δ whereas an electron in the higher energy eg subset contributes to a destabilisation of 35Δ
The final answer is then expressed as a multiple of the crystal field splitting parameter Δ (Delta)
Based on this, the crystal field stabilisation energies for d0 to d10 configurations can then be used to calculate the Octahedral Site Preference Energies which is defined as OSPE = CFSE (oct) - CFSE (tet)
Note: The conversion between Δoct and Δtet used for these calculations is
Δtet=Δoct×49