Photophysics of a Ruthenium Complex with a π‑Extended Dipyridophenazine Ligand for DNA Quadruplex Labeling

The light-switch mechanism of the complex [Ru­(bpy)₂(Br-dpqp)]­(PF₆)₂ (1, bpy = 2,2′-bipyridine, Br-dpqp = 12-bromo-14-ethoxydipyrido­[3,2-a:2′,3′-c]­quinolino­[3,2-h]­phenazine), i.e., a light-up probe for the selective labeling of G-quadruplexes, is investigated by time-resolved transient absorption and emission spectroscopy. We show that, in contrast to the prototypical light-switch complex [Ru­(bpy)₂(dppz)]­(PF₆)₂ (2, dppz = dipyrido­[3,2-a:2′,3′-c]­phenazine), a ³ππ* state localized on the π-extended ligand is the state determining the excited-state properties in both protic and aprotic environments. In aprotic environments, emission originates from a bright ³MLCT_phen state, which is thermally accessible from the ³ππ* state at ambient temperature. In the presence of water, i.e., in environments resembling in cellulo situations, the thermally accessible ³MLCT state is altered and becomes close in energy to the ³ππ* state, which induces a rapid excited-state deactivation of the ³ππ* state and a comparably weak emission.