The
low temperature emission spectra of metal acetylacetonate complexes are
analyzed. Excited state distortions are determined by using a
combination of resonance Raman spectroscopy, emission spectroscopy, and
time-dependent theory. The bonds that are most highly distorted as
a result of the transition are the C−C and O−C−C bonds on the
ligand, supporting an assignment of the emission to a ligand-centered
π−π* transition.