The Excited‐State Creutz–Taube Ion.

The excited‐state version of the Creutz–Taube ion was prepared via visible light excitation of [(NH3)5RuII(μ‐pz)RuII(NH3)5]4+. The resulting excited state is a mixed valence {RuIII–δ(μ‐pz⋅−)RuII+δ} transient species, which was characterized using femtosecond transient absorption spectroscopy with vis‐NIR detection. Very intense photoinduced intervalence charge transfers were observed at 7500 cm−1, revealing an excited‐state electronic coupling element HDA=3750 cm−1. DFT calculations confirm a strongly delocalized excited state. A notable consequence of strong electron delocalization is the nanosecond excited state lifetime, which was exploited in a proof‐of‐concept intermolecular electron transfer. The excited‐state Creutz–Taube ion is established as a reference, and demonstrates that electron delocalization in the excited state can be leveraged for artificial photosynthesis or other photocatalytic schemes based on electron transfer chemistry. [ABSTRACT FROM AUTHOR]