Modulation of ground and excited state properties of ruthenium complexes through sequential incorporation of metal into a polypyridyl-imidazole bridging ligand.

Abstract

A polypyridyl-imidazole-based bridging ligand, 2-(4-(4,5-di(pyridine-2-yl)-1H-imidazole-2-yl)phenyl)-1H-imidazo[4,5-f][1,10]phenanthroline (phen-H2PhImz-bpy), possessing three bidentate coordinating sites, has been designed in this work. The bridging ligand is employed to synthesize mono-, bi-, and trimetallic Ru(II) complexes in combination with terminal bipyridine units for the systematic modulation of photophysical and redox properties upon sequential incorporation of the metal unit into the bridge. All the compounds are characterized via NMR spectroscopy and electrospray ionization mass spectrometry. Absorption and both steady-state and time-resolved emission spectroscopic investigations of the ligand as well as Ru(II) complexes are thoroughly conducted in different solvents. The redox behaviors of the complexes are examined through cyclic voltammetry (CV) in acetonitrile. The focus of the investigation is centered on the systematic modulation of MLCT absorption and emission as well as the redox behavior of the complex entity upon the gradual incorporation of the Ru2+ unit into the complex backbone. The emission energy, quantum yield and lifetime are found to decrease systematically with an increase in the Ru2+ unit in the complex backbone and a linear relationship is observed in each case. A good correlation is also observed between the emission energies of complexes with their respective ΔE1/2 values (the difference between the first oxidation and first reduction potential).