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Isomer effects in fragmentation of Polycyclic Aromatic Hydrocarbons

  • M. H. Stockett*
  • , M. Gatchell
  • , N. De Ruette
  • , L. Giacomozzi
  • , T. Chen
  • , P. Rousseau
  • , S. Maclot
  • , J. Y. Chesnel
  • , L. Adoui
  • , B. A. Huber
  • , U. Běrziņš
  • , H. T. Schmidt
  • , H. Zettergren
  • , H. Cederquist
  • *Corresponding author for this work
  • Stockholm University
  • Aarhus University
  • Normandie University
  • Université de Caen Basse-Normandie

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

We have observed significant differences in the fragmentation patterns of isomeric Polycyclic Aromatic Hydrocarbon (PAH) cations following collisions with helium atoms at center-of-mass energies around 100 eV. This is in contrast to the situation at other collision energies or in photo-absorption experiments where isomeric effects are very weak and where the lowest-energy dissociation channels (H- and C2H2-loss) dominate in statistical fragmentation processes. In the 100 eV range, non-statistical fragmentation also competes and is uniquely linked to losses of single carbon atoms (CHx-losses). We find that such CHx-losses are correlated with the ionic ground state energy within a given group of isomers. We present results for three C16H10+, four C18H12+ and five C20H12+ isomers colliding with He.

Original languageEnglish
Pages (from-to)58-62
Number of pages5
JournalInternational Journal of Mass Spectrometry
Volume392
DOIs
Publication statusPublished - 3 Dec 2015

Keywords

  • Isomers
  • Non-statistical fragmentation
  • Polycyclic Aromatic Hydrocarbons

OECD Field of Science

  • 1.3 Physical Sciences

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