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dc.creatorWang, Hailingen_US
dc.creatorZhuang, Xiujuanen_US
dc.creatorSteimle, Timothy C.en_US
dc.creatorLinton, Colanen_US
dc.date.accessioned2009-07-29T12:53:02Z
dc.date.available2009-07-29T12:53:02Z
dc.date.issued2009en_US
dc.identifier2009-RF-04en_US
dc.identifier.urihttp://hdl.handle.net/1811/38209
dc.descriptionA.G. Adam; A.D. Granger; L.E. Downie; D.W. Tokaryk and C. Linton \textit {Can.J. Phys.R. Li, R.J. Jensen, W.J. Balfour, S.A. Shepard and A.G. Adam; \textit {J.Chem.Phys.J.J. Harrison, J.M. Brown, M.A. Flory, P.M. Sheridan, S.K. McLamarrah and L.M. Ziurys \textit {J. Chem. Phys.en_US
dc.descriptionAuthor Institution: Department of Chemistry and Biochemistry, Arizona State University, Tempe,AZ 85287; Center for Lasers, Atomic and Molecular Sciences and Physics Department, University of New Brunswick, Fredericton, NB Canada E3B 5A3en_US
dc.description.abstractRecently the New Brunswick group (accepted).} reported on the detection and analysis of the $B^{3}$$\Phi_{4}-X^{3}\Phi_{4}$ band system of IrF. The free-jet expansion conditions limited the spectral resolution to approximately 200 MHz, which was insufficient to fully resolve the $^{191}$Ir(I=3/2), $^{193}$Ir(I=3/2)and $^{19}$F(I=1/2)magnetic hyperfine splitting. Here we report on the analysis of the same band system recorded under molecular beam conditions which resulted in a resolution of 40 MHz. A simple molecular orbital correlation diagram is used to rationalize the determined parameters of IrF and the isovalent molecules RhF {\textbf{121}} 2591, 2004.} and CoF {\textbf{127}} 194308, 2007.}.en_US
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleANALYSIS OF THE MAGNETIC HYPERFINE STRUCTURE IN THE $B^{3}$$\Phi_{4}-X^{3}\Phi_{4}$ BAND SYSTEM OF IRIDIUM MONOFLUORIDE, IrFen_US
dc.typeArticleen_US


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