Highly Self-Organized Electron Transfer from an Iridium Complex to p-Benzoquinone Due to Formation of a π-Dimer Radical Anion Complex Triply Bridged by Scandium Ions

Unusually high kinetic order was observed in self-organized Sc3+-promoted electron transfer from tris(2-phenylpyridine)iridium(III) [Ir(ppy)3] to p-benzoquinone (Q) in propionitrile, third-order with respect to the concentration of Sc3+ and second-order with respect to the concentration of Q, to produce a π-dimer semiquinone radical anion complex that is triply bridged by three Sc3+ ions (Q•-−3Sc3+−Q).