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Exploring Differences in Lanthanide Excited State Reactivity Using a Simple Example: The Photophysics of La and Ce
Maksim Y Livshits1, Nikki J Wolford1, Jenny K Banh1
1Los Alamos National Laboratory (LANL), P.O. Box 1663, Los Alamos, New Mexico 87545, United States.
Abstract:
A series of four lanthanide thenoyltrifluoroacetone (TTA) complexes consisting of two f0 (La3+ and Ce4+) and two f1 (Ce3+) complexes was examined using steady-state and time-resolved spectroscopic techniques. The wide range of spectroscopic techniques presented herein have enabled us to discern the nature of the excited states (charge transfer, CT vs ligand localized, LL) as well as construct a Jablonski diagram for detailing the excited state reactivity within the series of molecules. The wavelength and excitation power dependence for these series of complexes are the first direct verification for the presence of simultaneous competing, noninteracting CT and LL excited states. Additionally, a computational framework is described that can be used to support spectroscopic assignments as a guide for future studies. Finally, the relationship between the obtained photophysics and possible photochemical separation mechanisms is described.
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