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Electrochemical Behavior of Phosphine-Substituted Ruthenium(II) Polypyridine Complexes with a Single Labile Ligand

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https://figshare.com/articles/dataset/Electrochemical_Behavior_of_Phosphine_Substituted_Ruthenium_II_Polypyridine_Complexes_with_a_Single_Labile_Ligand/2272477
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A series of phosphine-substituted ruthenium polypyridine complexes, cis­(P,Cl)-[Ru­(trpy)­(Pqn)­Cl]­PF6 (cis-Cl), trans­(P,MeCN)-[Ru­(trpy)­(Pqn)­(MeCN)]­(PF6)2 (trans-PN), cis­(P,MeCN)-[Ru­(trpy)­(Pqn)­(MeCN)]­(PF6)2 (cis-PN), and [Ru­(trpy)­(dppbz)­(MeCN)]­(PF6)2 (PP), were synthesized and crystallographically characterized (trpy = 2,2′:6′,2″-terpyridine, Pqn = 8-(diphenylphosphanyl)­quinoline, and dppbz = 1,2-bis­(diphenylphosphanyl)­benzene). In electrochemical measurements for cis-PN and PP, the reduction of cis-PN resulted in the formation of trans-PN via cis–trans isomerization and that of PP proceeded via a two-electron-transfer reaction. The mechanism of the electrochemical behaviors is discussed through consideration of five-coordinated species, [Ru­(trpy)­(Pqn)]n+ or [Ru­(trpy)­(dppbz)]n+ (n = 0–2), formed by liberation of a monodentate labile ligand.
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2016-02-17
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