Colour in Coordination Compounds
Coordination compounds are notable for their rich variety of colors, which arise primarily from electronic transitions of d electrons within the metal ion. When light interacts with these compounds, specific wavelengths are absorbed while others are reflected or transmitted, resulting in the observed color.
According to crystal field theory, the presence of ligands around a central metal ion leads to the splitting of d orbitals into two energy levels—higher and lower energy—depending on the geometry of the complex (e.g., octahedral, tetrahedral).
Key Points:
- Complementary Colour: The color seen is the complementary color of the absorbed light.
- Crystal Field Splitting: The arrangement of ligands influences the degree of splitting of d orbitals and thus affects the color observed.
- Example - [Ti(H2O)6]3+: This complex absorbs blue-green light, resulting in its violet appearance.
In a systematic exploration, various coordination entities like [CoCl(NH3)5] and [Cu(H2O)4] illustrate the relationship between absorbed wavelengths and the colors produced, emphasizing how different ligands can modify the electronic structure of the metal ion, ultimately leading to different observed colors.