Rotationally selected product pair correlation in F+CD4 -> DF(nu('))+CD3(nu=0,N)

doi:10.1063/1.1689634

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DC 欄位	值	語言
dc.contributor.author	Zhou, JG	en_US
dc.contributor.author	Shiu, WC	en_US
dc.contributor.author	Lin, JJ	en_US
dc.contributor.author	Liu, KP	en_US
dc.date.accessioned	2014-12-08T15:39:25Z	-
dc.date.available	2014-12-08T15:39:25Z	-
dc.date.issued	2004-04-01	en_US
dc.identifier.issn	0021-9606	en_US
dc.identifier.uri	http://dx.doi.org/10.1063/1.1689634	en_US
dc.identifier.uri	http://hdl.handle.net/11536/26915	-
dc.description.abstract	The 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.iso	en_US	en_US
dc.title	Rotationally selected product pair correlation in F+CD4 -> DF(nu('))+CD3(nu=0,N)	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1063/1.1689634	en_US
dc.identifier.journal	JOURNAL OF CHEMICAL PHYSICS	en_US
dc.citation.volume	120	en_US
dc.citation.issue	13	en_US
dc.citation.spage	5863	en_US
dc.citation.epage	5866	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:000220269100002	-
dc.citation.woscount	39	-
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