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Phys Chem Chem Phys


Title:"A SIFT-MS study of positive and negative ion chemistry of the ortho-, meta- and para-isomers of cymene, cresol, and ethylphenol"
Author(s):Swift SJ; Sixtova N; Omezzine Gnioua M; Spanel P;
Address:"J. Heyrovsky Institute of Physical Chemistry of CAS, v.v.i, Dolejskova 2155/3, 182 23 Prague, Czechia. stefan.swift@jh-inst.cas.cz. Faculty of Mathematics and Physics, Charles University, Ke Karlovu 3, 120 00 Prague, Czechia"
Journal Title:Phys Chem Chem Phys
Year:2023
Volume:20230712
Issue:27
Page Number:17815 - 17827
DOI: 10.1039/d3cp02123h
ISSN/ISBN:1463-9084 (Electronic) 1463-9076 (Linking)
Abstract:"Selected Ion Flow Tube Mass Spectrometry (SIFT-MS) is a soft ionisation technique based on gas phase ion-molecule reaction kinetics for the quantification of trace amounts of volatile organic compound vapours. One of its previous limitations is difficulty in resolving isomers, although this can now be overcome using different reactivities of several available reagent cations and anions (H(3)O(+), NO(+), O(2)(+) , O(-) , OH(-), O(2)(-) , NO(2)(-), NO(3)(-)). Thus, the ion-molecule reactions of these eight ions with all isomers of the aromatic compounds cymene, cresol and ethylphenol were studied to explore the possibility of their immediate identification and quantification without chromatographic separation. Rate coefficients and product ion branching ratios determined experimentally for the 72 reactions are reported. DFT calculations of their energetics confirmed the feasibility of the suggested reaction pathways. All positive ion reactions proceeded fast but largely did not discriminate between the isomers. The reactivity of the anions was much more varied. In all cases, OH(-) reacts by proton transfer forming (M-H); NO(2)(-) and NO(3)(-) were unreactive. The differences observed for product ion branching ratios can be used to identify isomers approximately"
Keywords:
Notes:"PubMed-not-MEDLINESwift, Stefan J Sixtova, Nikola Omezzine Gnioua, Maroua Spanel, Patrik eng England 2023/06/28 Phys Chem Chem Phys. 2023 Jul 12; 25(27):17815-17827. doi: 10.1039/d3cp02123h"

 
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