Electron Ionization of Imidazole and Its Derivative 2-Nitroimidazole.

Appearance energy Electron ionization Gas phase Imidazole Nitroimidazole Transition state Unimolecular dissociation

Journal

Journal of the American Society for Mass Spectrometry
ISSN: 1879-1123
Titre abrégé: J Am Soc Mass Spectrom
Pays: United States
ID NLM: 9010412

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 10 05 2019
accepted: 08 09 2019
revised: 02 08 2019
pubmed: 2 11 2019
medline: 1 5 2020
entrez: 1 11 2019
Statut: ppublish

Résumé

Imidazole (IMI) is a basic building block of many biologically important compounds. Thus, its electron ionization properties are of major interest and essential for the comparison with other molecular targets containing its elemental structure. 2-Nitroimidazole (2NI) contains the imidazole ring together with nitrogen dioxide bound to the C2 position, making it a radiosensitizing compound in hypoxic tumors. In the present study, we investigated electron ionization of IMI and 2NI and determined the mass spectra, the ionization energies, and appearance energies of the most abundant fragment cations. The experiments were complemented by quantum chemical calculations on the thermodynamic thresholds and potential energy surfaces, with particular attention to the calculated transition states for the most important dissociation reactions. In the case of IMI, substantially lower threshold values (up to ~ 1.5 eV) were obtained in the present work compared to the only available previous electron ionization study. Closer agreement was found with recent photon ionization values, albeit the general trend of slightly higher values for the case of electron ionization. The only exception for imidazole was found in the molecular cation at m/z 40 which is tentatively assigned to the quasi-linear HCCNH

Identifiants

pubmed: 31667709
doi: 10.1007/s13361-019-02337-w
pii: 10.1007/s13361-019-02337-w
pmc: PMC6914720
doi:

Substances chimiques

Imidazoles 0
Ions 0
Nitroimidazoles 0
imidazole 7GBN705NH1
azomycin K8E96XL55D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2678-2691

Subventions

Organisme : Austrian Science Fund FWF
ID : P 30332
Pays : Austria
Organisme : Austrian Science Fund (FWF)
ID : P30332

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Auteurs

Rebecca Meißner (R)

Institut für Ionenphysik und Angewandte Physik and Center for Molecular Biosciences Innsbruck (CMBI), Universität Innsbruck, Technikerstraße 25, 6020, Innsbruck, Austria. rebecca.meissner@uibk.ac.at.
Atomic and Molecular Collisions Laboratory, CEFITEC, Department of Physics, Universidade NOVA de Lisboa, 2829-516, Caparica, Portugal. rebecca.meissner@uibk.ac.at.

Linda Feketeová (L)

Institut für Ionenphysik und Angewandte Physik and Center for Molecular Biosciences Innsbruck (CMBI), Universität Innsbruck, Technikerstraße 25, 6020, Innsbruck, Austria. l.feketeova@ipnl.in2p3.fr.
Institut de Physique des 2 Infinis de Lyon; CNRS/IN2P3, UMR5822, Université de Lyon, Université Claude Bernard Lyon 1, 43 Bd du 11 novembre 1918, 69622, Villeurbanne, France. l.feketeova@ipnl.in2p3.fr.

Anita Ribar (A)

Institut für Ionenphysik und Angewandte Physik and Center for Molecular Biosciences Innsbruck (CMBI), Universität Innsbruck, Technikerstraße 25, 6020, Innsbruck, Austria.

Katharina Fink (K)

Institut für Ionenphysik und Angewandte Physik and Center for Molecular Biosciences Innsbruck (CMBI), Universität Innsbruck, Technikerstraße 25, 6020, Innsbruck, Austria.

Paulo Limão-Vieira (P)

Atomic and Molecular Collisions Laboratory, CEFITEC, Department of Physics, Universidade NOVA de Lisboa, 2829-516, Caparica, Portugal.

Stephan Denifl (S)

Institut für Ionenphysik und Angewandte Physik and Center for Molecular Biosciences Innsbruck (CMBI), Universität Innsbruck, Technikerstraße 25, 6020, Innsbruck, Austria. stephan.denifl@uibk.ac.at.

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Classifications MeSH