Mk. Nazeeruddin et al., ENHANCED INTENSITIES OF THE LIGAND-TO-METAL CHARGE-TRANSFER TRANSITIONS IN RU(III) AND OS(III) COMPLEXES OF SUBSTITUTED BIPYRIDINES, Journal of physical chemistry, 97(38), 1993, pp. 9607-9612
Ru(III) and Os(III) complexes of 2,2'-bipyridine carrying electron-don
or substituents show fairly intense ligand-to-metal charge-transfer (L
MCT) absorption band(s) in the red/near-IR region. The intensity of th
e LMCT band increases with increasing effective donor strength of the
substituted bpy ligand. The variations in the energies and intensities
of these LMCT bands has been examined in twenty complexes of the type
M(X2-bpy)3]3+ and M(bpy)n(X2-bpy)3-n]3+ (M = Ru or Os, X = Me, OMe, N
H2, and NMe2). In the homo trischelates the energy of the low-energy L
MCT transition falls within a narrow range of 1.80 +/- 0.1 V for Ru(II
I) and 2.20 +/- 0.1 V for Os(III). The energy of the LMCT transition i
s much lower in mixed-ligand complexes. A quantitative analysis as a f
unction of donor strength and Hammett substituent constants is present
ed.