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MLCT excited states. Role of the hydrido ligand in hydrido polypyridyl complexes of osmium(II) and ruthenium(II)

Journal Article · · Inorganic Chemistry; (USA)
DOI:https://doi.org/10.1021/ic00321a011· OSTI ID:7071164
;  [1]
  1. Univ. of North Carolina, Chapel Hill (USA)
The photochemical and photophysical properties of the complexes (M(bpy){sub 2}(CO)X)PF{sub 6} (bpy = 2,2{prime}-bipyridine; M = Os, X = H, D, Cl; M = Ru, X = H, D) are reported in 4:1 ethanol/methanol solution from 90 to 300 K. Metal to ligand charge-transfer (MLCT) excitation fails to induce metal hydride photochemistry, but oxidative or reductive quenching of (Os(bpy){sub 2}(CO)H){sup +*} does induce a net redox chemistry. There is no evidence for significant contributions to the emission spectrum nor to nonradiative decay by the {nu}(Os-H) mode. For the analogous complex of Ru, there is a significant {nu}(Ru-H) k{sub H}/k{sub D} kinetic isotope effect for nonradiative decay. 37 refs., 4 figs., 4 tabs.
OSTI ID:
7071164
Journal Information:
Inorganic Chemistry; (USA), Journal Name: Inorganic Chemistry; (USA) Vol. 28:22; ISSN 0020-1669; ISSN INOCA
Country of Publication:
United States
Language:
English