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

• Published in: Journal of physics. B, Atomic, molecular, and optical physics Vol. 57; no. 23; pp. 235101 - 235116
• Main Authors: 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
• Format: Journal Article
• Language: English
• Published: United Kingdom IOP Publishing 13.12.2024
• Subjects: covariance analysis; extreme ultraviolet spectroscopy; free electron laser spectroscopy; ion spectroscopy; molecular dynamics; site-selective ionization
• ISSN: 0953-4075; 1361-6455; 1361-6455
• DOI: 10.1088/1361-6455/ad8799

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 (C n H x + or C n H x 2 + , 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 C 6 H x 2 + 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.