Designing tridentate ligands for ruthenium(ii) complexes with prolonged room temperature luminescence lifetimes

Abstract

Coordination complexes have been used extensively as the photoactive component of artificial photosynthetic devices. While polynuclear arrays increase the probability of light absorption, the incorporation of the stereogenic Ru(2,2′-bipyridine)₃ ²⁺ motif gives rise to diastereomeric mixtures whereas the achiral Ru(2,2′:6′,2″-terpyridine)₂ ²⁺ motif creates stereopure polynuclear complexes. Thus, polynuclear arrays composed of ruthenium(II) complexes of tridentate ligands are the targets of choice for light-harvesting devices. As Ru(II) complexes of tridentate ligands have short excited state lifetimes at room temperature (r. t.), considerable effort has been focused on trying to increase their r. t. luminescence lifetime for practical applications. This tutorial review will report on the sophisticated synthetic strategies currently in use to enhance the room temperature photophysical properties of Ru(II) complexes of tridentate ligands.