Sj. Hug et Sg. Boxer, DIPOLAR CHARACTER OF LIGAND-CENTERED TRANSITIONS IN TRANSITION-METAL TRIS-BIPYRIDYL COMPLEXES, Inorganica Chimica Acta, 242(1-2), 1996, pp. 323-327
The Stark spectra of bipyridine (bpy) and the metaltris(2,2'-bipyridin
e) complexes of Zn, Fe, Ru and Os have been measured in the ligand-cen
tered region in the near UV. The results show that excitation into the
se ligand-centered absorption bands of the metal complexes leads to ex
cited states with dipole moments that are substantially larger than wo
uld be expected were the transitions purely ligand-centered. The diffe
rence dipoles between ground and excited states are 4.6 +/- 0.3 D/f fo
r Ru, 3.5 +/- 0.3 D/f for Os, 2.2 +/- 0.2 D/f for Fe, 1.4 +/- 0.2 D/f
for Zn and 0.5 +/- 0.5 D/f for free bpy (f is the local field correcti
on: 1.1-1.3). The values of the excited state dipole moments roughly c
orrelate with the separation between the UV ligand-centered bands and
the visible MLCT bands. possible mixing of ligand-centered excited sta
tes with MLCT states is discussed.