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Photochemistry of hetero-tris-chelated ruthenium(II) polypyridine complexes in dichloromethane

Journal Article · · Inorganic Chemistry; (USA)
DOI:https://doi.org/10.1021/ic00311a008· OSTI ID:5197288
 [1];  [2];  [3];  [4];
  1. Univ. of North Carolina, Chapel Hill (USA)
  2. Univ. of Vermont, Burlington (USA)
  3. IBM Corp., Essex Junction, VT (USA)
  4. Rensselaer Polytechnic Institute, Troy, NY (USA)

The results of an investigation of the photochemical and photophysical properties of a series of complexes of the type (RuL{sub 2}L{prime})Cl{sub 2} are reported, where L and L{prime} are bipyridine, phenanthroline, and methyl and phenyl derivatives of those ligands. All measurements were conducted in CH{sub 2}Cl{sub 2}. Luminescence lifetime and quantum yield data indicate that the ligand which accepts the electron in the localized MLCT excited state plays a significant role in the excited-state decay. HPLC analysis of the organic photoproducts from mixed-ligand complexes shows that flexible bipyridyl ligands are preferentially photolabilized, consistent with a dissociative mechanism involving an open-ended bipyridine in the transition state. 55 refs., 2 tabs.

OSTI ID:
5197288
Journal Information:
Inorganic Chemistry; (USA), Journal Name: Inorganic Chemistry; (USA) Journal Issue: 12 Vol. 28:12; ISSN 0020-1669; ISSN INOCA
Country of Publication:
United States
Language:
English