Photophysical Dynamics and Relaxation Pathways of Ligand-to-Metal Charge-Transfer States in the 5f1 [Np(VI)O2Cl4]2- Anion

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2017-03, Vol.121 (12), p.2353-2360
• Main Authors: Barker, Beau J, Berg, John M, Kozimor, Stosh A, Wozniak, Nicholas R, Wilkerson, Marianne P
• Format: Article
• Language: English
• Subjects: INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/acs.jpca.7b01029

Although several publications report on the electronic structure of the neptunyl ion, experimental measurements to detail the photophysical dynamics of this open-shell actinyl system are limited in number. Time-resolved photoluminescence has been a useful experimental approach for understanding photophysical dynamics and relaxation pathways of a variety of other molecular and ionic systems, including gaseous plutonium hexafluoride and solid-state uranyl compounds. Here, we investigate time-resolved photoluminescence emission of the 5f1 neptunyl tetrachloride ([Np(VI)O2Cl4]2-) dianion following visible excitation. Photoemission of the lowest energy neptunyl ligand-to-metal charge-transfer (LMCT) transitions to both the ground and first electronically excited states is observed. Analyses of the decay lifetimes of the excited states suggest different relaxation pathways as a function of excitation energy. Vibronic progressions associated with the Np-oxo symmetric stretching mode are measured in emission spectra, and the energies from these progressions are compared with energies of vibronic progressions associated with the excitation spectra of [Np(VI)O2Cl4]2-. This study expands our understanding of this open-shell actinyl system beyond identification of excited states, allowing characterization of photophysical properties and evidence for the electronic character of the ground state, and suggests that this approach may be applicable to more complex actinide systems.