Wavelength-Dependent Photodissociation of Iodomethylbutane

Ultrashort XUV pulses of the Free-Electron-LASer in Hamburg (FLASH) were used to investigate laser-induced fragmentation patterns of the prototypical chiral molecule 1-iodo-2-methyl-butane (C$_5$H$_{11}$I) in a pump-probe scheme. Ion velocity-map images and mass spectra of optical-laser-induced fragmentation were obtained for subsequent FEL exposure with photon energies of 63 eV and 75 eV. These energies specifically address the iodine 4d edge of neutral and singly charged iodine, respectively. The presented ion spectra for two optical pump-laser wavelengths, i.e., 800 nm and 267 nm, reveal substantially different cationic fragment yields in dependence on the wavelength and intensity. For the case of 800-nm-initiated fragmentation, the molecule dissociates notably slower than for the 267-nm pump. The results underscore the importance of considering optical-laser wavelength and intensity in the dissociation dynamics of this prototypical chiral molecule that is a promising candidate for future studies of its asymmetric nature.

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Publication Details

Journal
ArXiv.org
Published
2025-01-01
DOI
https://doi.org/10.3204/pubdb-2025-02061
Primary Topic
Advanced Chemical Physics Studies
Type
article
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article

Wavelength-Dependent Photodissociation of Iodomethylbutane

Clemens von Korff Schmising, Daniel Rolles, R. Wagner, Felix Allum et al.
ArXiv.org
Advanced Chemical Physics Studies
article

Wavelength-Dependent Photodissociation of Iodomethylbutane

Clemens von Korff Schmising, Daniel Rolles, R. Wagner, Felix Allum, Arno Ehresmann, Ludger Inhester, Philipp Schmidt, Denis Kargin, Jason W. L. Lee, Patrik Grychtol, M. Brouard, Mats Larsson, Peter Walter, Valerija Music, Vitali Zhaunerchyk, Lucas Schwob, Bastian Manschwetus, Lutz Marder, Huda Otto, Robert Mason, Kaja Schubert, Christopher Passow, Benjamin Erk, Philipp V. Demekhin, Richard Thomas, Michael Burt, Günter Brenner, Rudolf Pietschnig, Claire Vallance, Igor Vidanović, T. Baumann, David Heathcote, Simon Dörner, Rebecca Boll, Sadia Bari, Michael Meyer, Zheng Li, Markus Ilchen, Daniel Ramm, Andreas Galler
article en

Abstract

Ultrashort XUV pulses of the Free-Electron-LASer in Hamburg (FLASH) were used to investigate laser-induced fragmentation patterns of the prototypical chiral molecule 1-iodo-2-methyl-butane (C$_5$H$_{11}$I) in a pump-probe scheme. Ion velocity-map images and mass spectra of optical-laser-induced fragmentation were obtained for subsequent FEL exposure with photon energies of 63 eV and 75 eV. These energies specifically address the iodine 4d edge of neutral and singly charged iodine, respectively. The presented ion spectra for two optical pump-laser wavelengths, i.e., 800 nm and 267 nm, reveal substantially different cationic fragment yields in dependence on the wavelength and intensity. For the case of 800-nm-initiated fragmentation, the molecule dissociates notably slower than for the 267-nm pump. The results underscore the importance of considering optical-laser wavelength and intensity in the dissociation dynamics of this prototypical chiral molecule that is a promising candidate for future studies of its asymmetric nature.

ArXiv.org
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Advanced Chemical Physics Studies
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