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

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...

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Bibliographic Details
Published in:Inorganic chemistry 1989-06, Vol.28 (12), p.2281-2285
Main Authors: Jones, Wayne E, Smith, Robert A, Abramo, Marsha T, Williams, Michael D, Van Houten, J
Format: Article
Language:English
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Summary: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.
ISSN:0020-1669
1520-510X
DOI:10.1021/ic00311a008