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dc.creatorMosley, J.en_US
dc.creatorHasbrouck, S.en_US
dc.creatorDuncan, M. A.en_US
dc.date.accessioned2011-07-12T17:38:24Z
dc.date.available2011-07-12T17:38:24Z
dc.date.issued2011en_US
dc.identifier2011-WJ-07en_US
dc.identifier.urihttp://hdl.handle.net/1811/49623
dc.descriptionAuthor Institution: Department of Chemistry, University of Georgia, Athens, GA 30602-2556en_US
dc.description.abstractCo$^+$Ne was generated via laser vaporization in a pulsed supersonic expansion source, mass selected, and analyzed by visible photodissociation spectroscopy. An electronic band system was observed with an origin beginning at 13529 cm$^{-1}$. A progression of fifteen peaks beginning from the origin until the convergence limit can be seen, corresponding to the vibrational bands in the excited state of Co$^+$Ne. The excited state constants ($\omega$$_e$'=113 cm$^{-1}$, $\omega$$_e$x$_e$'=4.76 cm$^{-1}$) were determined, and the electronic cycle leads to a ground state binding energy (D$_0$"=933 cm$^{-1}$). The ground state binding energy can be compared to other rare gas binding energies, which is correlated to the polarizability of the rare gas. Resolved rotational structure in the (0,0) transition gives the excited and ground state bond lengths.en_US
dc.language.isoenen_US
dc.publisherOhio State Universityen_US
dc.titleELECTRONIC SPECTROSCOPY OF COBALT-NEON CATIONen_US
dc.typeArticleen_US


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