Selected Ion Flow Tube Study of the Ion−Molecule Reactions of Monochloroethene, Trichloroethene, and Tetrachloroethene

详细信息    查看全文

• 作者：Victor A. Mikhailov ; Michael A. Parkes ; Matthew J. Simpson ; Richard P. Tuckett ; Chris A. Mayhew
• 刊名：Journal of Physical Chemistry A
• 出版年：2008
• 出版时间：September 25, 2008
• 年：2008
• 卷：112
• 期：38
• 页码：9012-9022
• 全文大小：249K
• 年卷期：v.112,no.38(September 25, 2008)
• ISSN：1520-5215

文摘

Data for the rate coefficients and product cations of the reactions of a large number of atomic and small molecular cations with monochloroethene, trichloroethene, and tetrachloroethene in a selected ion flow tube at 298 K are reported. The recombination energy of the ions range from 6.27 (H₃O⁺) through to 21.56 (Ne⁺) eV. Collisional rate coefficients are calculated by modified average dipole orientation theory and compared with experimental values. Thermochemistry and mass balance predict the most feasible neutral products. Together with previously reported results for the three isomers of dichloroethene (), the fragment ion branching ratios have been compared with those from threshold photoelectron photoion coincidence spectroscopy over the photon energy range of 9−22 eV to determine the importance or otherwise of long-range charge transfer. For ions with recombination energy in excess of the ionization energy of the chloroethene, charge transfer is energetically allowed. The similarity of the branching ratios from the two experiments suggest that long-range charge transfer is dominant. For ions with recombination energy less than the ionization energy, charge transfer is not allowed; chemical reaction can only occur following formation of an ion−molecule complex, where steric effects are more significant. The products that are now formed and their percentage yields are a complex interplay between the number and position of the chlorine atoms with respect to the CC bond, where inductive and conjugation effects can be important.