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

Felix N. Castellano, Henryk Malak, Ignacy Gryczynski, Joseph R. Lakowicz

Research output: Contribution to journalArticle

43 Scopus citations

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 deb 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.

Original languageEnglish
Pages (from-to)5548-5551
Number of pages4
JournalInorganic Chemistry
Volume36
Issue number24
DOIs
StatePublished - 1997

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