MeV Electron Diffractive Imaging of Competing Ring-Opening and Photodissociation
ORAL
Abstract
Here we present time-resolved MeV electron scattering results of 2-Iodothiophene and 3-Iodothiophene and interrogate the branching ratios between ring-opening and C-I bond cleavage following photoexcitation at 245 nm. After UV excitation, halothiophenes can either undergo ring-opening or prompt bond cleavage. The branching ratio between these processes is dependent on the wavelength, substitution position, and atom identity, as a result of the different substitution effects for the electron-withdrawing halogen. The use of ultrafast electron bunches to study time-resolved dynamics has become a powerful tool for probing transient geometries. Of particular interest is the ability to use this to quantitatively probe reactions that proceed along competing reaction coordinates. This time-resolved geometric comparison further elucidates the direct and indirect C-I cleavage processes identified in a recent coulomb explosion study of these same two isomers [1].
[1] W. Razmus et al. Exploring the Ultrafast and Isomer-Dependent Photodissociation of Iodothiophenes via Site-Selective Ionization (Submitted December 2023).
[1] W. Razmus et al. Exploring the Ultrafast and Isomer-Dependent Photodissociation of Iodothiophenes via Site-Selective Ionization (Submitted December 2023).
*A.M.G., M.B., F.A., B.K., K.L., J.G., and R.F. were supported by the Department of Energy Office of Basic Energy Science, Facilities Division. A.G., T.W., and P.H.B. were supported by the AMOS program within the U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. A.M.G. was additionally supported by an NSF Graduate Research Fellowship. The use of the MeV-UED instrument, which is operated as part of the Linac Coherent Light Source at the SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Contract No. DE-AC02-76SF00515.
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Presenters
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Aaron M Ghrist
- Stanford University