The optical spectrum of this d6 octahedral complex exhibits an intense absorption near 250 nm corresponding to a transition from ligand σ MO to the empty eg MO. In IrBr62−, which is a d5 complex, two absorptions, one near 600 nm and another near 270 nm, are observed. These are assigned as two LMCT bands, one to t2g and another to eg. The 600 nm band corresponds to transition to the t2g MO and the 270 nm band to the eg MO.
Charge transfer bands may also arise from transfer of electrons from nonbonding orbitals of the ligand to the eg MO.
The tetraoxides of d0 metal centers are often deeply colored for the first row metals. This coloration is assigned to LMCT, involving transfer of nonbonding electrons on the oxo ligands to empty d-levels on the metal. For heavier metals, these same transitions occur in the UV region, hence no color is observed. Hence perrhenate, tungstate, and molybdate are colorless.
The energies of transitions correlate with the order of the electrochemical series. The metal ions that are most easily reduced correspond to the lowest energy transitions. The above trend is consistent with transfer of electrons from the ligand to the metal, thus resulting in a reduction of metal ions by the ligand.
Complexes of bipyridine, phenanthroline, and related unsaturated heterocycles often exhibit strong C-T bands. Most famous is Ru(bipy)32+, which upon irradiation gives excited states described as [Ru(III)(bipy−)(bipy)2]2+. The CT excited state is long-lived, allowing a rich chemistry ensues.56
Intervalence charge transfer (IVCT) is a type of charge-transfer band that is associated with mixed-valence compounds. Unlike the usual MLCT or LMCT bands, the IVCT bands are lower in energy, usually in the visible or near-infrared region of the spectrum and is broad. Prussian blue, the blue pigment derived from Fe(III), Fe(II), and cyanide, owes its intense color to IVCT.
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