Atomic hydrogen interactions with gas-phase coronene cations: hydrogenation versus fragmentation. Issue 35 (27th June 2018)

• Record Type: Journal Article
• Authors: Rapacioli, Mathias; Cazaux, Stéphanie; Foley, Nolan; Simon, Aude; Hoekstra, Ronnie; Schlathölter, Thomas
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 35(2018)
• Page Start: 22427
• Page End: 22438
• Publication Date: 2018-06-27
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c8cp03024c
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Competition between hydrogenation and fragmentation of coronene: experimental and theoretical view. Abstract : Sequential hydrogenation of polycyclic aromatic hydrocarbon (PAH) cations drives a gradual transition from a planar to a puckered geometry and from an aromatic to an aliphatic electronic structure. The resulting H-induced weakening of the molecular structure together with the exothermic nature of the consecutive H-attachment processes can lead to substantial molecular fragmentation. We have studied H attachment to gas-phase coronene cations in a radiofrequency ion trap using tandem mass spectrometry. With increasing hydrogenation, C2 H i loss and multifragmentation are identified as main de-excitation channels. To understand the dependence of both channels on H-exposure time, we have simulated the molecular stability and fragmentation channels of hydrogenated PAHs using a molecular dynamics approach employing potential energies determined by a density functional based tight binding method. As the coronene fragmentation patterns depend on the balance between energy deposition by H-attachment and the extent of cooling in between subsequent attachment processes, we investigate several scenarios for the energy distribution of hydrogenated PAHs. Good agreement between experiment and simulation is reached, when realistic energy distributions are considered.