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Journal of University of Chinese Academy of Sciences ›› 2021, Vol. 38 ›› Issue (2): 207-216.DOI: 10.7523/j.issn.2095-6134.2021.02.007

• Research Articles • Previous Articles     Next Articles

Dissociative photoionization of methyl crotonate: experimental and theoretical insights

SUN Ruirui1, LI Yanbo2, CHEN Jun2, MENG Qinghui2, WANG Huanhuan2, ZHANG Hang2, SHAN Xiaobin2, LIU Fuyi2, SHENG Liusi2   

  1. 1. School of Physical Sciences, University of Science and Technology of China, Hefei 230026, China;
    2. National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029, China
  • Received:2019-03-29 Revised:2019-05-21 Online:2021-03-15
  • Supported by:
    Supported by the National Natural Science Foundation of China (11575178,41575126)

Abstract: The photoionization and dissociation of methyl crotonate have been studied by tunable vacuum ultraviolet synchrotron radiation coupled with time-of-flight mass spectrometer in the photon energy region 9.0-14.5 eV. The ionization energy of methyl crotonate and the appearance energies for major fragments C4H5O2+, C4H5O+,C4H4O+, C2H3O2+, C3H5+, and C2H5+ are determined to be 10.11, 10.73, 10.88, 12.2, 11.93(12.77), and 12.44 eV, respectively, according to the photoionization efficiency curves. Based on the experimental AEs and energies predicted by ab initio G3B3 calculations, possible formation channels for the major fragments C4H5O2++CH3, C4H5O++CH3O, C4H4O++CH4O, C2H3O2++C3H5, C3H5++C2H3O2(CO+CH3O), and C2H5++C3H3O2 are proposed. Transition states and intermediates involved in the dissociation channels are also located. The majority of the proposed channels occur through isomerization processes prior to dissociations. Hydrogen shift and ring closing/opening are found to be the dominant processes during photoionization and dissociation of methyl crotonate.

Key words: methyl crotonate, synchrotron radiation, mass spectrometry, dissociative photoionization, G3B3 calculations

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