Transition Metal Chemistry

, Volume 18, Issue 2, pp 197–204 | Cite as

Ruthenium(II) complexes with phenanthroline-, benzimidazole-, benzothiazole-, and pyridine-derived bidentate and tridentate ligands: reactivity and spectroscopic and electrochemical characterization

  • Michael R. McDevitt
  • Yu Ru
  • Anthony W. Addison
Full Papers


Ruthenium complexes of some tridentate and bidentate benzimidazole-, benzothiazole- and pyridine-derived ligands have been prepared as their PFf6p− salts, and their constitutions have been confirmed by elemental analysis, 1H-n.m.r. spectroscopy and electrochemistry. The complexes are redox-active, displaying a metal-centred RuII/ RuIII oxidation process and sequential ligand-localized reduction processes. Both the 2-(2′-pyridyl)benzimidazole complex [Ru(PybimH)3]2+ and the 2,2′-dipyridylamine one, [Ru(DpyaH)3]2+ behave as weak Brønsted-Lowry acids. The secondary amino nitrogen of each DpyaH in the [Ru(DpyaH)3]2+ complex can be deprotonated with hydride anion, and then acts as a strong nucleophile, allowing selective N-alkylation by alkyl halides. Most of the complexes exhibit ligand-localized luminescence emission at ambient temperature. The strong intrinsic fluorescences of 2-(2′-quinolyl)-N-methylbenzimidazole and 2-(2′-pyridyl)-benzimidazole are quenched when they are coordinated to RuII, and emission from the chelates entailing 5-nitro-1:10-phenanthroline occurs only from the non-nitrated ligands.


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Copyright information

© Chapman & Hall 1993

Authors and Affiliations

  • Michael R. McDevitt
    • 1
  • Yu Ru
    • 1
  • Anthony W. Addison
    • 1
  1. 1.Chemistry DepartmentDrexel UniversityPhiladelphiaUSA

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