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dc.contributor.authorZhou, JGen_US
dc.contributor.authorShiu, WCen_US
dc.contributor.authorLin, JJen_US
dc.contributor.authorLiu, KPen_US
dc.date.accessioned2014-12-08T15:39:25Z-
dc.date.available2014-12-08T15:39:25Z-
dc.date.issued2004-04-01en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.1689634en_US
dc.identifier.urihttp://hdl.handle.net/11536/26915-
dc.description.abstractThe title reaction was studied in a crossed-beam experiment by imaging of state-selected products. The rotational state selection of the CD3 products was achieved using (2+1) resonance-enhanced multiphoton ionization. The coincident information on the DF coproducts was revealed in a state-resolved manner from time-sliced velocity map images. Significant dependences of both the correlated differential cross sections and the DF vibrational branching ratios on the "tagged" CD3 rotation states were found. The dynamical implications of one of the major findings are discussed. (C) 2004 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleRotationally selected product pair correlation in F+CD4 -> DF(nu('))+CD3(nu=0,N)en_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.1689634en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume120en_US
dc.citation.issue13en_US
dc.citation.spage5863en_US
dc.citation.epage5866en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000220269100002-
dc.citation.woscount39-
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