Wavelength-Dependent Photodissociation of Iodomethylbutane

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

arXiv · 2502.16572

Wavelength-Dependent Photodissociation of Iodomethylbutane

View original source ↗Read source document ↗Export metadata ↓

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.

Explore related subjects

physics.chem-ph physics.atom-ph

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

Valerija Music, Felix Allum, Ludger Inhester, Philipp Schmidt, Rebecca Boll, Thomas M. Baumann, Günter Brenner, Mark Brouard, Michael Burt, Philipp V. Demekhin, Simon Dörner, Arno Ehresmann, Andreas Galler, Patrik Grychtol, David Heathcote, Denis Kargin, Mats Larsson, Jason W. L. Lee, Zheng Li, Bastian Manschwetus, Lutz Marder, Robert Mason, Michael Meyer, Huda Otto, Christopher Passow, Rudolf Pietschnig, Daniel Ramm, Daniel Rolles, Kaja Schubert, Lucas Schwob, Richard D. Thomas, Claire Vallance, Igor Vidanovic, Clemens von Korff Schmising, René Wagner, Vitali Zhaunerchyk, Peter Walter, Sadia Bari, Benjamin Erk, Markus Ilchen. 2025-02-23. Wavelength-Dependent Photodissociation of Iodomethylbutane. https://arxiv.org/abs/2502.16572

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

arXiv2026

Breaking Water at Graphene Defects

Water dissociation at solid surfaces underpins processes ranging from corrosion and catalysis to electrochemistry and photovoltaics. Defects often serve as reactive sites for dissociation, yet how solvation influences water dissociation at such sites remains poorly understood. Here, we use state-of-the-art machine-learned interatomic potentials to explore water dissociation at defective graphene-water interfaces. We show that solvation qualitatively changes the reaction mechanism at a graphene single vacancy (SV), opening pathways that are absent for an isolated water molecule. Whereas the gas-phase process proceeds via a single concerted channel, the solvated SV splits water through two competing pathways: a basic route forming SV-H and OH-(aq), and an acidic route forming SV-OH and H3O+(aq). These lower-barrier pathways produce distinct chemisorbed intermediates that enhance graphene-water adsorption. Accordingly, even a simple carbon vacancy gives rise to unexpectedly rich interfacial chemistry, coupling surface chemistry to interfacial charge and wettability, with implications for carbon functionalization and nanofluidic transport.

physics.chem-ph↗

arXiv2026

Comprehensive Study of L-Menthol and Octanoic Acid as a Hydrophobic Eutectic Solvent

Hydrophobic eutectic solvents (HES) based on natural compounds represent promising green alternatives to conventional solvents. In this work, we investigate the physicochemical, structural, and dynamical properties of an ES formed by L-menthol and octanoic acid using a combined experimental and molecular dynamics simulation approach. Five compositions with molar ratios from 1:3 to 3:1 were studied with molecular dynamics simulation in the temperature range 15 degrees C to 35 degrees C. Experimental measurements of density and viscosity in the temperature range from 5 degrees C to 35 degrees C were complemented with results obtained from MD simulations employing the OPLS force field. Structural analyses based on radial distribution functions and Kirkwood-Buff integrals reveal that the dominant interactions in the mixture are hydrogen bonds between L-menthol and octanoic acid molecules. Dynamic properties, including self-diffusion coefficients and hydrogen-bond lifetimes, indicate that intermolecular hydrogen bonds between the two components are stronger and longer-lived than bonds between identical species. These findings provide molecular-level insight into the structure and transport properties of menthol-based ESs relevant for green solvent applications.

physics.chem-ph↗

arXiv2026

More is not always better: Dissociative photoionization limits the EUV absorbing photacid generator pentafluorophenyl triflate in photolithography

Pentafluorophenyl triflate has been explored as a highly absorbing neutral photoacid generator (PAG) candidate for next generation chemically amplified resists used in extreme ultraviolet (EUV) lithography. Although increased fluorination enhances EUV absorption, this study demonstrates that such an approach does not necessarily improve photoacid generation efficiency. Using photoelectron-photoion coincidence (PEPICO) spectroscopy at the 92 eV photon energy of the EUV scanners in combination with quantum chemical calculations, the dissociative photoionization of pentafluorophenyl triflate was systematically investigated. The photoionization mass spectrum reveals extensive fragmentation, with the parent ion contributing only 3.1 % of the total signal and CF$_3^+$ representing the dominant product ion. Computed appearance energies align well with experimental trends and support a sequential fragmentation pathway involving loss of SO$_2$, CF$_3$, and CO. Crucially, none of the major dissociation channels yield precursors capable of forming triflic acid, the strong photoacid required for efficient deprotection reactions in chemically amplified resists. Combined with previous dissociative electron attachment studies indicating similarly unfavorable fragmentation, the results demonstrate that despite its high EUV absorption cross section, pentafluorophenyl triflate is unsuitable as a PAG for EUV lithography. The findings highlight the importance of understanding fundamental photoionization and electron interaction mechanisms to guide the rational design of next generation high performance EUV photoresists.

physics.chem-ph↗