Vacuum ultraviolet photoionization mass spectrometric study of cyclohexene. (4th February 2016)

• Record Type: Journal Article
• Authors: Chen, Jun; Cao, Maoqi; Wei, Bin; Ding, Mengmeng; Shan, Xiaobin; Liu, Fuyi; Sheng, Liusi
• Is Part Of: Journal of mass spectrometry. Volume 51:Number 2(2016)
• Page Start: 169
• Page End: 181
• Publication Date: 2016-02-04
• Subjects: cyclohexene -- synchrotron radiation -- photoionization -- photodissociation -- mass spectrometry; Mass spectrometry -- Periodicals; 543.65
• DOI: 10.1002/jms.3743
• Languages: English
• ISSNs: 1076-5174

Abstract

Abstract : In this work, photoionization and dissociation of cyclohexene have been studied by means of coupling a reflectron time‐of‐flight mass spectrometer with the tunable vacuum ultraviolet (VUV) synchrotron radiation. The adiabatic ionization energy of cyclohexene as well as the appearance energies of its fragment ions C6 H9 +, C6 H7 +, C5 H7 +, C5 H5 +, C4 H6 +, C4 H5 +, C3 H5 + and C3 H3 + were derived from the onset of the photoionization efficiency (PIE) curves. The optimized structures for the transition states and intermediates on the ground state potential energy surfaces related to photodissociation of cyclohexene were characterized at the ω B97X‐D/6‐31+g(d, p) level. The coupled cluster method, CCSD(T)/cc‐pVTZ, was employed to calculate the corresponding energies with the zero‐point energy corrections by the ω B97X‐D/6‐31+g(d, p) approach. Combining experimental and theoretical results, possible formation pathways of the fragment ions were proposed and discussed in detail. The retro‐Cope rearrangement was found to play a crucial role in the formation of C4 H6 +, C4 H5 + and C3 H5 + . Intramolecular hydrogen migrations were observed as dominant processes in most of the fragmentation pathways of cyclohexene. The present research provides a clear picture of the photoionization and dissociation processes of cyclohexene in the 8‐ to 15.5‐eV photon energy region. Copyright © 2016 John Wiley & Sons, Ltd.