Dissociative ionisation of adamantane: a combined theoretical and experimental study. Issue 8 (20th November 2017)

• Record Type: Journal Article
• Authors: Candian, Alessandra; Bouwman, Jordy; Hemberger, Patrick; Bodi, Andras; Tielens, Alexander G. G. M.
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 8(2018)
• Page Start: 5399
• Page End: 5406
• Publication Date: 2017-11-20
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c7cp05957d
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Adamantane, the smallest nanodiamond molecule, dissociates mostly through C4 H8 and C3 H7 loss, yielding small hydrocarbons as product. Abstract : Diamond nanoparticles, or nanodiamonds, are intriguing carbon-based materials which, maybe surprisingly, are the most abundant constituent of presolar grains. While the spectroscopic properties of even quite large diamondoids have already been explored, little is known about their unimolecular fragmentation processes. In this paper we characterise the dissociative ionisation of adamantane (C10 H16 ) – the smallest member of the diamondoid family – utilising imaging Photoelectron Photoion Coincidence (iPEPICO) spectroscopy and Density Functional Theory (DFT) calculations. We have found adamantane to dissociatively photoionise via several parallel channels of which H, C3 H7 and C4 H8 losses are the most important ones. Calculations confirm the existence of a rate-limiting transition state for the multiple C-loss channels, which is located at 10.55 eV with respect to neutral adamantane. In addition, we found dissociation channels leading to small cationic hydrocarbons, which may be relevant in the interstellar medium.