Creation of Metal-to-Ligand Charge Transfer Excited States with Two-Photon Excitation

Abstract

We examined the steady state and time-resolved emission spectral properties of [Ru(bpy)₃]²⁺ and [Ru(bpy)₂-(dcb)]²⁺, where bpy is 2,2'-bipyridine and dcb is 2,2'-bipyridine-4,4'-dicarboxylic acid, in fluid solution when excited with 90 fs pulses from a mode-locked Ti/sapphire laser. Over the wavelength range 820-900 nm, both complexes displayed two-photon excitation as observed by a quadratic dependence of the emission intensity on incident power. Steady state emission and time-resolved frequency-domain intensity decay measurements revealed that two-photon excitation of each complex resulted in the same emission spectra and single-exponential decays as observed for one-photon excitation at a variety of temperatures in different solvents. The two-photon excitation cross section of [Ru(bpy)₃]²⁺ measured at 880 nm was determined to be 4.3 × 10^-50 cm⁴ s/photon. These results clearly show that metal-to-ligand charge transfer (MLCT) excited states can in fact be obtained through multiphoton processes.