Collision-induced dissociation dynamics of the [OCS • C2H2]+ complex. A combined experimental and theoretical study

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Publication Type Journal Article
School or College College of Science
Department Chemistry
Creator Armentrout, Peter B.
Other Author Muntean, Felician
Title Collision-induced dissociation dynamics of the [OCS • C2H2]+ complex. A combined experimental and theoretical study
Date 2000
Description Collision-induced dissociation (CID) of the [OCS • C2H2]+ complex ion with both Xe and Ar over an energy range of 0 to 10 eV in the center of mass frame is studied using a guided ion beam tandem mass spectrometer. The cross sections of the ionic products observed (C,H2S+, OCS+, C2HJ, and S+) are analyzed by taking into account reactant energy distributions, multiple collisions, lifetime effects and competition. A recently devised statistical model for the simultaneous analysis of competitive product channels is used to analyze three channels for the first time, with good results. Thresholds for product formation at 0 Kelvin are 0.33+0.07 eV for C2H2S+, 0.95+0.07 eV for OCS+, 1.22+0.08 eV for C2H,, and an upper limit of 4.26 eV for S+.
Type Text
Publisher Oldenbourg Verlagsgruppe
Volume 214
Issue 8
First Page 1035
Last Page 1063
Subject Collision-induced dissociation; Competitive shift; Ethylene Sulfide cation; Kinetic shift; Thioketene cation; Potential energy surface
Subject LCSH Excited state chemistry; Reactivity (Chemistry); Dissociation; Thermochemistry
Language eng
Bibliographic Citation Muntean, F., & Armentrout, P. B. (2000). Collision-induced dissociation dynamics of the [OCS • C2H2]+ complex. A combined experimental and theoretical study. Zeitschrift für Physikalische Chemie, 214(8), 1035-63.
Rights Management (c)Oldenbourg Verlagsgruppe
Format Medium application/pdf
Format Extent 1,552,418 bytes
Identifier ir-main,8056
ARK ark:/87278/s6dv238f
Setname ir_uspace
ID 704796
Reference URL https://collections.lib.utah.edu/ark:/87278/s6dv238f
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