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dc.contributor.authorFang, Jing-Wenen_US
dc.contributor.authorXie, Tingxianen_US
dc.contributor.authorChen, Hsueh-Yingen_US
dc.contributor.authorLu, Yu-Juen_US
dc.contributor.authorLee, Yuan T.en_US
dc.contributor.authorLin, Jim J.en_US
dc.date.accessioned2019-04-02T05:59:39Z-
dc.date.available2019-04-02T05:59:39Z-
dc.date.issued2009-04-23en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp811053den_US
dc.identifier.urihttp://hdl.handle.net/11536/149770-
dc.description.abstractThe reaction of F-2 + C3H6 has been investigated with the crossed molecular beam technique. The only observed primary product channel is F + C3H6F while the HF + C3H5F channel cannot be found. The reaction cross section was measured as a function of collision energy and the reaction threshold was determined to be 2.4 +/- 0.3 kcal/mol. Compared to the reaction threshold of the F-2 + C2H4 reaction, the methyl substitution effectively reduces the reaction threshold by about 3 kcal/mol. The product time-of-flight spectra and angular distributions were measured and analyzed. The angular distribution displays strongly backward, indicating that the reaction is much faster than rotation. All experimental results support a rebound reaction mechanism, which agrees with the structure of the calculated transition state. The transition state geometry also suggests an early barrier; such dynamics is consistent with the observed small kinetic energy release of the products. Except for the different values of the reaction thresholds, the dynamics of the F-2 + C2H4 and F-2 + C3H6 reactions are remarkably similar.en_US
dc.language.isoen_USen_US
dc.titleDynamics of the F-2 Reaction with Propene: The Effect of Methyl Substitutionen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp811053den_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Aen_US
dc.citation.volume113en_US
dc.citation.spage4381en_US
dc.citation.epage4386en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000265383200083en_US
dc.citation.woscount7en_US
Appears in Collections:Articles