Many coordination compounds are brightly coloured, and their colours are due to electronic transitions within the d-orbitals of the central metal ion. The observed colour depends on factors such as the type of metal ion, its oxidation number, and the ligands coordinated to it.
The colour of a complex compound mainly arises due to d-d transitions. When white light falls on a complex, certain wavelengths are absorbed as electrons jump between split d-orbitals. The portion of light that is not absorbed and instead reflected or transmitted is what gives the complex its visible colour.
When ligands surround the central metal ion in a coordination complex, the originally equal-energy d-orbitals split into two distinct energy levels. This is known as crystal field splitting.
For example, in an octahedral field, the d-orbitals split into two sets: lower energy t2g and higher energy eg. When electrons absorb energy equal to the gap between these levels (Δ), they get excited from t2g to eg.
Complexes with completely filled (d10) or empty (d0) d-orbitals do not show d-d transitions, so they appear colourless. Example: [Zn(H2O)6]²⁺ is colourless as Zn²⁺ has d10 configuration.
Understanding the cause of colour in complex compounds is important in JEE Main. Questions may involve identifying coloured ions, predicting colour changes based on ligand strength, or applying crystal field theory concepts.