The crystal field stabilization energy (CFSE) is influenced by the metal's oxidation state and the ligand's field strength.
General principles dictate:
- A higher metal oxidation state correlates with a stronger ligand field and consequently a higher CFSE.
- \( \text{NH}_3 \) functions as a stronger field ligand than \( \text{en} \) (ethylenediamine).
Consequently, the following relationships apply: - \( [\text{Co(NH}_3)_4]^{2+} \) exhibits the lowest CFSE due to its lower oxidation state.
- Compared to \( [\text{Co(NH}_3)_4]^{2+} \), \( [\text{Co(NH}_3)_6]^{2+} \) displays a higher CFSE.
- \( [\text{Co(NH}_3)_6]^{3+} \) has a higher CFSE than \( [\text{Co(NH}_3)_6]^{2+} \) due to its elevated oxidation state.
- \( [\text{Co(en)}_3]^{3+} \) possesses the highest CFSE, attributed to the potent ligand field exerted by \( \text{en} \).
Therefore, the order of CFSE is:
\[[\text{Co(NH}_3)_4]^{2+} < [\text{Co(NH}_3)_6]^{2+}<[\text{Co(NH}_3)_6]^{3+} < [\text{Co(en)}_3]^{3+}\]