The dissociative recombination of hydrocarbon ions. III. Methyl-substituted benzene ring compounds

Autor: C. Rebrion-Rowe, T Mostefaoui, J. B. A. Mitchell, Sylvain Laubé
Přispěvatelé: Physique des atomes, lasers, molécules et surfaces (PALMS), Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2000
Předmět:
Zdroj: Journal of Chemical Physics
Journal of Chemical Physics, American Institute of Physics, 2000, 113 (8), ⟨10.1063/1.1286974⟩
Journal of Chemical Physics, 2000, 113 (8), ⟨10.1063/1.1286974⟩
ISSN: 1089-7690
0021-9606
DOI: 10.1063/1.1286974
Popis: International audience; The recombination of electrons with cyclic ions produced via ion – molecule reactions between atomic precursor ions and methyl-substituted benzene ring compounds ͑(toluene , ortho-, and para-xylene and mesitylene) has been studied at 300 K using a flowing afterglow Langmuir probe-mass spectrometer apparatus. Differing amounts of energy can be deposited into the daughter ions depending upon which atomic precursor is used. It has been found that same-mass daughter ions formed from different precursors displayed different recombination rate coefficients indicating that different isomeric forms were reacting. In particular , the benzene ring of the toluene cation expands to a seven-membered ring following isomerization to the cycloheptatriene form. H atom abstraction allows two different isomeric daughter ions to be formed that do not interconvert and that display different recombination rates. A similar behavior was observed for the xylenes and for mesitylene. All recombination rates lie in the range from 10-7 to 10 -6 cm3 s-1 and display no apparent relation with size nor with the aromaticity of the ions .
Databáze: OpenAIRE