| 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 | ©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 |