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Identification of the roaming mechanism and the formation of H3+ in core ionised cyclopropane

Lindblom, Ville LU orcid ; Ganguly, Smita LU ; Walsh, Noelle LU ; Gisselbrecht, Mathieu LU orcid and Sorensen, Stacey L. LU orcid (2026) In Physical Chemistry Chemical Physics 28(12). p.7344-7351
Abstract

Spectroscopic validation of the roaming process in molecular dissociation was first reported for formaldehyde, but today roaming is acknowledged to be a nearly ubiquitous dissociation pathway. The process has been described as a frustrated dissociation process, and as such, direct detection of the roaming process is challenging. In the present study the cyclopropane dication is the starting point for a roaming process that results in the production of H3+. In our experiment, we measure the complete momenta of all charged fragments and unravel the kinematics for relevant fragmentation processes. We present a comprehensive study of the process comparing alternative pathways for dissociation and their kinematics in... (More)

Spectroscopic validation of the roaming process in molecular dissociation was first reported for formaldehyde, but today roaming is acknowledged to be a nearly ubiquitous dissociation pathway. The process has been described as a frustrated dissociation process, and as such, direct detection of the roaming process is challenging. In the present study the cyclopropane dication is the starting point for a roaming process that results in the production of H3+. In our experiment, we measure the complete momenta of all charged fragments and unravel the kinematics for relevant fragmentation processes. We present a comprehensive study of the process comparing alternative pathways for dissociation and their kinematics in association to the roaming process. In this study, inner-shell electron ionisation leads to dication states, these final electronic states are fundamentally identical to ones reached via direct double ionisation.

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author
; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Physical Chemistry Chemical Physics
volume
28
issue
12
pages
8 pages
publisher
Royal Society of Chemistry
external identifiers
  • scopus:105031743920
  • pmid:41774538
ISSN
1463-9076
DOI
10.1039/d5cp04926a
language
English
LU publication?
yes
additional info
Publisher Copyright: This journal is © the Owner Societies, 2026
id
be788e37-d77f-4e83-8a59-fa131852b980
date added to LUP
2026-08-16 16:04:50
date last changed
2026-08-18 03:29:09
@article{be788e37-d77f-4e83-8a59-fa131852b980,
  abstract     = {{<p>Spectroscopic validation of the roaming process in molecular dissociation was first reported for formaldehyde, but today roaming is acknowledged to be a nearly ubiquitous dissociation pathway. The process has been described as a frustrated dissociation process, and as such, direct detection of the roaming process is challenging. In the present study the cyclopropane dication is the starting point for a roaming process that results in the production of H<sub>3</sub><sup>+</sup>. In our experiment, we measure the complete momenta of all charged fragments and unravel the kinematics for relevant fragmentation processes. We present a comprehensive study of the process comparing alternative pathways for dissociation and their kinematics in association to the roaming process. In this study, inner-shell electron ionisation leads to dication states, these final electronic states are fundamentally identical to ones reached via direct double ionisation.</p>}},
  author       = {{Lindblom, Ville and Ganguly, Smita and Walsh, Noelle and Gisselbrecht, Mathieu and Sorensen, Stacey L.}},
  issn         = {{1463-9076}},
  language     = {{eng}},
  month        = {{02}},
  number       = {{12}},
  pages        = {{7344--7351}},
  publisher    = {{Royal Society of Chemistry}},
  series       = {{Physical Chemistry Chemical Physics}},
  title        = {{Identification of the roaming mechanism and the formation of H<sub>3</sub>+ in core ionised cyclopropane}},
  url          = {{http://dx.doi.org/10.1039/d5cp04926a}},
  doi          = {{10.1039/d5cp04926a}},
  volume       = {{28}},
  year         = {{2026}},
}