Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhou, JG | en_US |
dc.contributor.author | Lin, JJ | en_US |
dc.contributor.author | Liu, KP | en_US |
dc.date.accessioned | 2014-12-08T15:38:49Z | - |
dc.date.available | 2014-12-08T15:38:49Z | - |
dc.date.issued | 2004-07-08 | en_US |
dc.identifier.issn | 0021-9606 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1063/1.1761051 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/26569 | - |
dc.description.abstract | The 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.iso | en_US | en_US |
dc.title | Observation of a reactive resonance in the integral cross section of a six-atom reaction: F+CHD3 | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1063/1.1761051 | en_US |
dc.identifier.journal | JOURNAL OF CHEMICAL PHYSICS | en_US |
dc.citation.volume | 121 | en_US |
dc.citation.issue | 2 | en_US |
dc.citation.spage | 813 | en_US |
dc.citation.epage | 818 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000222265600024 | - |
dc.citation.woscount | 50 | - |
Appears in Collections: | Articles |
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