Valence shell threshold photoelectron spectroscopy of C3Hx (x = 0–3). Issue 13 (14th March 2018)

• Record Type: Journal Article
• Authors: Garcia, Gustavo A.; Gans, Bérenger; Krüger, Julia; Holzmeier, Fabian; Röder, Anja; Lopes, Allan; Fittschen, Christa; Alcaraz, Christian; Loison, Jean-Christophe
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 13(2018)
• Page Start: 8707
• Page End: 8718
• Publication Date: 2018-03-14
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c8cp00510a
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : We present the photoelectron spectra of C3 H x ( x = 0–3) formed in a microwave discharge flow-tube reactor by consecutive H abstractions from C3 H4 (C3 H x + F → C3 H x− 1 + HF ( x = 1–4)), but also from F + CH4 schemes by secondary reactions. Abstract : We present the photoelectron spectra of C3 H x ( x = 0–3) formed in a microwave discharge flow-tube reactor by consecutive H abstractions from C3 H4 (C3 H x + F → C3 H x −1 + HF ( x = 1–4)), but also from F + CH4 schemes by secondary reactions. The spectra were obtained combining tunable VUV synchrotron radiation with double imaging electron/ion coincidence techniques, yielding mass-selected threshold photoelectron spectra. The obtained results complement not only existing ones, but for the first time the photoelectron spectra of C3, cyclic and linear C3 H (c, l-C3 H) as well as of the excited states of C3 H3 are reported. In the case of c-C3 H, l, t-C3 H2 and C3 H3, Franck–Condon simulations have been performed in order to assign the vibrational structure. The adiabatic ionization energies of these radicals are reported and compared to ab initio calculated values as well as to theoretical values using known enthalpies of formation.