DIPOLAR CHARACTER OF LIGAND-CENTERED TRANSITIONS IN TRANSITION-METAL TRIS-BIPYRIDYL COMPLEXES

Authors
Citation
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
Citations number
17
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201693
Volume
242
Issue
1-2
Year of publication
1996
Pages
323 - 327
Database
ISI
SICI code
0020-1693(1996)242:1-2<323:DCOLTI>2.0.ZU;2-S
Abstract
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.