A solution of \([Ni(H_2O)_6]^{2+}\) is green but a solution of \([Ni(CN)_4]^{2-}\) is colourless. Explain.
In\( [Ni(H_2O)_6]^{ 2+}\) ,\(H_2\ddot{O}\) is a weak field ligand. Therefore, there are unpaired electrons in \(Ni^{2+}\). In this complex, the delectrons from the lower energy level can be excited to the higher energy level i.e., the possibility of \(d - d\) transition is present. Hence, \(Ni(H_2O)_6]^{ 2+}\) is coloured. In \([Ni(CN)_4] ^{2-} \), the electrons are all paired as \(CN^{ -}\) is a strong field ligand. Therefore, d-d transition is not possible in \([Ni(CN)_4]^{ 2-}\) . Hence, it is colourless.
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.