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Distinguishing the XUV-induced Coulomb explosion dynamics of iodobenzene using covariance analysis

Walmsley, Tiffany; Allum, Felix; Harries, James R; Kumagai, Yoshiaki; Lim, Suzanne; McManus, Joseph; Nagaya, Kiyonobu; Britton, Mathew; Brouard, Mark; Bucksbaum, Philip; Fushitani, Mizuho; Gabalski, Ian; Gejo, Tatsuo; Hockett, Paul; Howard, Andrew J; Iwayama, Hiroshi; Kukk, Edwin; Lam, Chow-shing; Minns, Russell S; Niozu, Akinobu; Nishimuro, Sekito; Niskanen, Johannes; Owada, Shigeki; Razmus, Weronika O; Rolles, Daniel; Somper, James; Ueda, Kiyoshi; Unwin, James; Wada, Shin-ichi; Woodhouse, Joanne L; Forbes, Ruaridh; Burt, Michael; Warne, Emily M

Distinguishing the XUV-induced Coulomb explosion dynamics of iodobenzene using covariance analysis

Walmsley, Tiffany
Allum, Felix
Harries, James R
Kumagai, Yoshiaki
Lim, Suzanne
McManus, Joseph
Nagaya, Kiyonobu
Britton, Mathew
Brouard, Mark
Bucksbaum, Philip
Fushitani, Mizuho
Gabalski, Ian
Gejo, Tatsuo
Hockett, Paul
Howard, Andrew J
Iwayama, Hiroshi
Kukk, Edwin
Lam, Chow-shing
Minns, Russell S
Niozu, Akinobu
Nishimuro, Sekito
Niskanen, Johannes
Owada, Shigeki
Razmus, Weronika O
Rolles, Daniel
Somper, James
Ueda, Kiyoshi
Unwin, James
Wada, Shin-ichi
Woodhouse, Joanne L
Forbes, Ruaridh
Burt, Michael
Warne, Emily M
Katso/Avaa
Walmsley_2024_J._Phys._B__At._Mol._Opt._Phys._57_235101.pdf (2.505Mb)
Lataukset: 

IOP Publishing
doi:10.1088/1361-6455/ad8799
URI
http://doi.org/10.1088/1361-6455/ad8799
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025082791897
Tiivistelmä

The primary and secondary fragmentation dynamics of iodobenzene following its ionization at 120 eV were determined using three-dimensional velocity map imaging and covariance analysis. Site-selective iodine 4d ionization was used to populate a range of excited polycationic parent states, which primarily broke apart at the carbon-iodine bond to produce I+ with phenyl or phenyl-like cations (CnHx+ or CnHx2+, with n  =  1 – 6 and x  =  1 – 5). The molecular products were produced with varying degrees of internal excitation and dehydrogenation, leading to stable and unstable outcomes. This further allowed the secondary dynamics of C6Hx2+ intermediates to be distinguished using native-frame covariance analysis, which isolated these processes in their own centre-of-mass reference frames. The mass resolution of the imaging mass spectrometer used for these measurements enabled the primary and secondary reaction channels to be specified at the level of individual hydrogen atoms, demonstrating the ability of covariance analysis to comprehensively measure the competing fragmentation channels of aryl cations, including those involving intermediate steps.

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