Experimental and theoretical study on the dissociative photoionization of trans-2-methyl-2-butenal

被引:1
作者
Li, Yuquan [1 ]
Cao, Maoqi [1 ]
Chen, Jun [1 ]
Song, Yanlin [1 ]
Shan, Xiaobin [1 ]
Zhao, Yujie [1 ]
Liu, Fuyi [1 ]
Wang, Zhenya [2 ]
Sheng, Liusi [1 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Sch Nucl Sci & Technol, Hefei 230029, Peoples R China
[2] Chinese Acad Sci, Anhui Inst Opt & Fine Mech, Lab Environm Spect, Hefei 230031, Peoples R China
关键词
Trans-2-methyl-2-butenal; Synchrotron radiation; Dissociative photoionization; Theoretical calculation; CBS-QB3; VOLATILE ORGANIC-COMPOUNDS; SET MODEL CHEMISTRY; GAS-PHASE; SYNCHROTRON-RADIATION; TRANS-CROTONALDEHYDE; 193; NM; EMISSIONS; ACROLEIN; PHOTODISSOCIATION; IONIZATION;
D O I
10.1016/j.molstruc.2014.03.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dissociative photoionization of trans-2-methyl-2-butenal was investigated with photoionization mass spectrometer in photon energy region between 8.97 and 15 eV. The ionization energy (IE) of trans-2-methyl-2-butenal and the appearance energies (AEs) of major fragment ions C5H7O+, C4H5O+, C4H8+, C4H7+, C3H5+, C3H4+, C2H4+, CHO+, C2H4O+ and C3H3+ are obtained to be 9.57, 10.71, 10.68, 10.59, 11.55, 11.94, 11.82, 12.03, 12.21, 12.09 and 12.90 eV respectively by measurement of the photoionization efficiency curves (PIEs). Based on the experimental results, six major dissociative photoionization channels, C5H7O+ + H, C4H5O+ + CH3, C5H6+ + H2O, C4H8+ + CO (-> C3H5+ + CH3 + CO, C3H4+ + CH4 + CO, C2H4+ + C2H4+ CO, C4H7+ + H + CO), C4H7+ + CHO (C4H7 + CHO+), and C3H4 + C2H4O+ are proposed with the aid of theoretical calculations at the level of CBS-QB3. Both direct dissociation and isomerization of the parent ion exist during the fragment forming procedure. H shift and ring formation are found to be dominant in the isomerization of the parent ion. Transition states and intermediates involved in the dissociation channels are also determined. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:130 / 139
页数:10
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