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dc.contributor.authorZhou, JGen_US
dc.contributor.authorLin, JJen_US
dc.contributor.authorLiu, KPen_US
dc.date.accessioned2014-12-08T15:38:49Z-
dc.date.available2014-12-08T15:38:49Z-
dc.date.issued2004-07-08en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.1761051en_US
dc.identifier.urihttp://hdl.handle.net/11536/26569-
dc.description.abstractThe title reaction was investigated under crossed-beam conditions at collisional energies ranging from about 0.4 to 7.5 kcal/mol. Product velocity distributions were measured by a time-sliced, velocity-map imaging technique to explicitly account for the density-to-flux transformation factors. Both the state-resolved, pair-correlated excitation functions and vibrational branching ratios are presented for the two isotopic product channels. An intriguing resonance tunneling mechanism occurring near the reaction threshold for the HF+CD3 product channel is surmized, which echoes the reactive resonances found previously for the F+HD-->HF+D reaction and more recently for the F+CH4 reaction. (C) 2004 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleObservation of a reactive resonance in the integral cross section of a six-atom reaction: F+CHD3en_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.1761051en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume121en_US
dc.citation.issue2en_US
dc.citation.spage813en_US
dc.citation.epage818en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000222265600024-
dc.citation.woscount50-
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