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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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Published in: | Inorganic chemistry 1989-06, Vol.28 (12), p.2281-2285 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 0020-1669 1520-510X |
DOI: | 10.1021/ic00311a008 |