SearcharxivSearch

arXiv · 1709.01739

Observation of Concerted and Stepwise Multiple Dechlorination Reactions of Perchlorethylene in Electron Ionization Mass Spectrometry According to Measured Chlorine Isotope Effects

Abstract

Dechlorinated fragmental ions of organochlorines can be commonly found on electron ionization-mass spectrometry (EI-MS). Yet it is still unclear whether multiple dechlorination reactions taking place in EI-MS are concerted or stepwise. This study investigated the concertedness of the multiple dechlorination reactions of perchlorethylene (PCE) in EI-MS in light of the observed chlorine isotope effects during different dechlorination reactions along with the detected MS signal intensities. The fluctuant isotope ratios among different ions revealed that the observed multiple dechlorinated reactions in the EI-DFS-HRMS were stepwise. And the changing trends of isotope ratios of the ions detected by EI-qMS might suggest that the observed multiple dechlorination reactions in this MS were concerted. Mechanisms for these concerted/stepwise multiple dechlorination reactions are tentatively interpreted. Besides the evidence of isotope effects, according to the quasi-equilibrium theory, the MS signal intensities also suggested that the multiple dechlorination reactions in the EI-HRMS were likely stepwise, while those in the EI-qMS might be concerted. The distance from the ionization region to the mass analyzer entrance in an MS may be a critical factor affecting the dechlorination reactions of ions flying over this distance. This distance in the EI-qMS is significantly shorter than that in the EI-HRMS. Thus, the main detected ions in the EI-qMS might be generated during the ionization and in-source fragmentation processes, while the main ions detected in the EI-HRMS might be produced during the fragmentation of precursor ions flying over the distance. We deduce that the main dechlorination reactions in the ionization region were concerted, while those taking place during the flight of precursor ions over the distance from the ionization region to the mass analyzer entrance were stepwise.

Explore related subjects

Keep this discovery

BibTeXRIS

Caiming Tang, Jianhua Tan. 2017-09-06. Observation of Concerted and Stepwise Multiple Dechlorination Reactions of Perchlorethylene in Electron Ionization Mass Spectrometry According to Measured Chlorine Isotope Effects. https://arxiv.org/abs/1709.01739

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

KEEP EXPLORING

Related papers

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

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

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