Phosphorescent Trinuclear Pt-Ir-Pt Complexes: Insights into the Photophysical and Electrochemical Properties and Interaction with Guanine Nucleobase.

Abstract

In this study we have analysed the comparative photophysical and electrochemical properties of two isomeric heterotrinuclear PtII -IrIII -PtII complexes 3 and 6 and the four corresponding intermediate isomeric homonuclear cyclometalated iridium(III) complexes 1, 2, 4 and 5. The isomerisation originates from positional differences in the formyl, di-2-picolylamine and Pt-di-2-picolylamine moieties appended to cyclometalated or ancillary ligands. The interaction of 5'-GMP with the trinuclear complexes 3 and 6 shows that platinum centres appended to the cyclometalated ligand in 3 facilitate the binding of two 5'-GMP units per PtII centre in preference to a single 5'-GMP unit per PtII centre as observed in 6. The 1:2 and 1:1 PtII -5'-GMP binding patterns probably arise from the convenient arrangements of the Pt-di-2-picolylamine units in different planes in complex 3, which is absent in complex 6.