4.6 Article

2-(1H-1,2,3-Triazol-4-yl)-Pyridine Ligands as Alternatives to 2,2 '-Bipyridines in Ruthenium(II) Complexes

Journal

CHEMISTRY-AN ASIAN JOURNAL
Volume 4, Issue 1, Pages 154-163

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.200800297

Keywords

click chemistry; coordination chemistry; ruthenium; UV/Vis spectroscopy; supramolecular chemistry

Funding

  1. Nederlandse Organisatie voor Wetenschappelijk Onderzock
  2. Fonds der Chernischen Industrie

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The synthesis of a variety of 2-(1H-1,2,3-triazol-4-yl)-pyridines by click chemistry is demonstrated to provide straightforward access to mono-functionalized ligands. The ring-opening polymerization of E-caprolactone initiated by such a mono-functionalized ligand highlights the synthetic potential of this class of bidentate ligands with respect to polymer chemistry or the attachment onto surfaces and nanoparticles. The coordination to Ru-11 ions results in homoleptic and heteroleptic complexes with the resultant photophysical and electrochemical properties strongly dependent on the number of these ligands attached to the Ru-11 core.

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