Abstract
Two redox-asymmetric amide-bridged bis(terpyridine)ruthenium(II) complexes (3a, 3b) have been prepared by amide coupling of a carboxylic acid functionalized complex with an amine substituted complex and they were fully characterized by spectroscopic analyses. They emit at 692 and 750nm at room temperature in fluid solution with quantum yields larger than 10−3 and 3MLCT lifetimes of 22ns. Ru···Ru distances were estimated from DFT models as 17.7 and 13.4Å for 3a and 3b, respectively. Cyclic voltammetry gives two oxidation potentials for the differently substituted ruthenium sites with splittings of 0.10 and 0.23V for 3a and 3b, respectively. Oxidation of 3b with CeIV ions gives the corresponding mixed-valent RuII–RuIII system which is valence-localized according to NIR spectroscopic and theoretical analyses.
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