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Identification of the fragment of the 1-methylpyrene cation by mid-IR spectroscopy.
Jusko, Pavol; Simon, Aude; Wenzel, Gabi; Brünken, Sandra; Schlemmer, Stephan; Joblin, Christine.
Afiliação
  • Jusko P; Institut de Recherche en Astrophysique et Planétologie (IRAP), Université de Toulouse (UPS), CNRS, CNES, 9 Av. du Colonel Roche, 31028 Toulouse Cedex 4, France.
  • Simon A; I. Physikalisches Institut, Universität zu Käoln, Zülpicher Str. 77, 50937 Köln, Germany.
  • Wenzel G; Laboratoire de Chimie et Physique Quantiques LCPQ/IRSAMC, Université de Toulouse (UPS) and CNRS, 118 Route de Narbonne, 31062 Toulouse, France.
  • Brünken S; Institut de Recherche en Astrophysique et Planétologie (IRAP), Université de Toulouse (UPS), CNRS, CNES, 9 Av. du Colonel Roche, 31028 Toulouse Cedex 4, France.
  • Schlemmer S; Radboud University, Institute for Molecules and Materials, FELIX Laboratory, Toernooiveld 7c, 6525 ED Nijmegen, The Netherlands.
  • Joblin C; I. Physikalisches Institut, Universität zu Käoln, Zülpicher Str. 77, 50937 Köln, Germany.
Chem Phys Lett ; 698: 206-210, 2018 Apr 16.
Article em En | MEDLINE | ID: mdl-29882538
ABSTRACT
The fragment of the 1-methylpyrene cation, C17H11+, is expected to exist in two isomeric forms, 1-pyrenemethylium PyrCH2+ and the tropylium containing species PyrC7+. We measured the infrared (IR) action spectrum of cold C17H11+ tagged with Ne using a cryogenic ion trap instrument coupled to the FELIX laser. Comparison of the experimental data with density functional theory calculations allows us to identify the PyrCH2+ isomer in our experiments. The IR Multi-Photon Dissociation spectrum was also recorded following the C2H2 loss channel. Its analysis suggests combined effects of anharmonicity and isomerisation while heating the trapped ions, as shown by molecular dynamics simulations.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article