Investigating the ultraviolet photodissociation of bromocyclopropane with ultrafast electron diffraction

We have studied the photodissociation of gas-phase bromocyclopropane by 200 nm wavelength ultraviolet radiation using ultrafast electron diffraction. Bromocyclopropane is a prototypical molecule in the study of organobromides, a class of molecules that have a significant impact on atmospheric ozone depletion through their photochemistry. Previous studies have revealed two possible reaction pathways for the photodissociation of bromine from bromocyclopropane; either the C-Br bond dissociates, leaving behind a cyclopropyl ring, or there is a concerted opening of the cyclopropyl ring along with the C-Br bond dissociation. In this work, both our experimental and simulation results indicate that the majority of the UV-photoexcited BCP molecules (88% ± 11% in the experiment) follow the first reaction pathway, in which the cyclopropyl ring remains closed after homolytic C-Br bond cleavage. This direct bond dissociation occurs within the experimental time resolution of 270 fs. In order to differentiate between the possible reaction end-products, both of which have diffraction signals dominated by the bromine atom, a new analysis method has been employed, which is more sensitive to the structure of the end-products.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-11-04
DOI
https://doi.org/10.1063/5.0293140
Citations
2
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
2.60
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article

Investigating the ultraviolet photodissociation of bromocyclopropane with ultrafast electron diffraction

Stephen Weathersby, Cuong Le, Andrew J. Orr‐Ewing, Fuhao Ji et al.
2 citations
The Journal of Chemical Physics
Atmospheric chemistry and aerosols
2.60
article

Investigating the ultraviolet photodissociation of bromocyclopropane with ultrafast electron diffraction

Stephen Weathersby, Cuong Le, Andrew J. Orr‐Ewing, Fuhao Ji, Martin Centurion, Ming‐Fu Lin, Yusong Liu, Sajib Kumar Saha, Xiaozhe Shen, Conor D. Rankine, Duan Luo, Kareem Hegazy, Andrew Attar, Yanwei Xiong, Thomas Wolf, Xijie Wang, Kyle Wilkin, Jie Yang, J. Pedro F. Nunes, Matthew R. Ware, J. Lederer
article en
2 citations

Abstract

We have studied the photodissociation of gas-phase bromocyclopropane by 200 nm wavelength ultraviolet radiation using ultrafast electron diffraction. Bromocyclopropane is a prototypical molecule in the study of organobromides, a class of molecules that have a significant impact on atmospheric ozone depletion through their photochemistry. Previous studies have revealed two possible reaction pathways for the photodissociation of bromine from bromocyclopropane; either the C-Br bond dissociates, leaving behind a cyclopropyl ring, or there is a concerted opening of the cyclopropyl ring along with the C-Br bond dissociation. In this work, both our experimental and simulation results indicate that the majority of the UV-photoexcited BCP molecules (88% ± 11% in the experiment) follow the first reaction pathway, in which the cyclopropyl ring remains closed after homolytic C-Br bond cleavage. This direct bond dissociation occurs within the experimental time resolution of 270 fs. In order to differentiate between the possible reaction end-products, both of which have diffraction signals dominated by the bromine atom, a new analysis method has been employed, which is more sensitive to the structure of the end-products.

The Journal of Chemical PhysicsVol. 163(17)
University of Nebraska–Lincoln (US), TU Dortmund University (DE), SLAC National Accelerator Laboratory (US), Diamond Light Source (GB), University of Bristol (GB), University of York (GB), University of Duisburg-Essen (DE), Tsinghua University (CN)
Openalex Percentile: Top 9%
Atmospheric chemistry and aerosols
2.60
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