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Updated: Jun 19, 2025

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Predissociation-based measurements of bond dissociation energies: US2, OUS, and USe
Kimberly H Tomchak1, Jason J Sorensen1, Erick Tieu1
1Department of Chemistry, University of Utah, Salt Lake City, Utah 84112-0850, USA.
Abstract:
The uranium-containing molecules US2, OUS, and USe have been investigated using a pulsed laser ablation supersonic beam molecular source with time-of-flight mass spectrometric detection. Spectra have been recorded using the resonant two-photon ionization method over the spectroscopic range from 277 to 238 nm. These species have a myriad of excited electronic states in this spectroscopic region, leading to spectra that are highly congested and appear quasicontinuous. Sharp predissociation thresholds are observed, allowing precise bond dissociation energies to be measured. In the case of the triatomic molecules, it was necessary to use one laser for excitation and a delayed laser for ionization in order to observe a sharp predissociation threshold that allowed a precise bond dissociation energy to be measured. The resulting thermochemical values are D0(SU-S) = 4.910 ± 0.003 eV, D0(OU-S) = 5.035 ± 0.004 eV, and D0(USe) = 4.609 ± 0.009 eV. These results provide the first measurement of D0(USe) and reduce the error limits in the previous values of D0(SU-S) and D0(OU-S) by a factor of more than 70.
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