Abstract
The photoinduced energy and structural relaxation of aqueous iron(II)-tris-bipyridine ([FeII(bpy)3]2+), upon excitation into its singlet metal-to-ligand charge transfer (1MLCT) band, and the population of its short-lived (?0.6 ns) high-spin excited state have been characterized by combined ultrafast optical and X-ray spectroscopies. Polychromatic femtosecond fluorescence up-conversion reveals a very short lived 1MLCT emission band, which decays in ?20 fs by intersystem crossing to a 3MLCT, whose very weak emission is also observed. Transient absorption studies show that the latter decays in
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