Definition:
Ionization isomerism occurs in coordination compounds when two isomers produce different ions in solution, even though they have the same overall composition. This happens due to the exchange of groups between the coordination sphere and the ionization sphere.
Key Idea:
Example:
Consider the following two complexes: \[ [Co(NH_3)_5SO_4]Br \quad \text{and} \quad [Co(NH_3)_5Br]SO_4 \]
- The first complex in aqueous solution gives: \[ [Co(NH_3)_5SO_4]Br \;\;\rightarrow\;\; [Co(NH_3)_5SO_4]^+ + Br^- \] Hence, it produces \(Br^-\) ions in solution.
- The second complex in aqueous solution gives: \[ [Co(NH_3)_5Br]SO_4 \;\;\rightarrow\;\; [Co(NH_3)_5Br]^ {2+} + SO_4^{2-} \] Hence, it produces \(SO_4^{2-}\) ions in solution.
Ionization isomers are coordination compounds that yield different ions in solution. Example: \[ [Co(NH_3)_5SO_4]Br \quad \text{and} \quad [Co(NH_3)_5Br]SO_4 \] are ionization isomers.
The correct IUPAC name of \([ \text{Pt}(\text{NH}_3)_2\text{Cl}_2 ]^{2+} \) is:
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
What is crystal field splitting energy?
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
On the basis of CFT, explain why [Ti(H$_2$O)$_6$]Cl$_3$ complex is coloured? What happens on heating the complex [Ti(H$_2$O)$_6$]Cl$_3$? Give reason.