Energy transfer from rhenium(i) complexes to covalently attached anthracenes and phenanthrenes

Abstract

The synthesis and photophysical properties of a series of chromophore–quencher complexes are reported. They are all comprised of a luminescent rhenium(I) tricarbonyl diimine complex that is covalently attached to anthracene or phenanthrene moieties via rigid rod-like p-xylene bridges of variable lengths. Rhenium-to-anthracene energy transfer is strongly exergonic (−ΔG⁰≈ 0.9 eV) and causes very efficient rhenium MLCT luminescence quenching. By contrast, rhenium-to-phenanthrene energy transfer is only observed when complexes with sufficiently high MLCT energies are used because for these dyads, the driving force for energy transfer is low (−ΔG⁰≈ 0.1 eV). For a ∼15 Å donor–acceptor distance, the rate constants of the weakly and the strongly exergonic energy transfer processes differ by more than 3 orders of magnitude.