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dc.creatorO'Brien, James J.en_US
dc.creatorO'Brien, L. C.en_US
dc.date.accessioned2006-06-15T19:15:34Z
dc.date.available2006-06-15T19:15:34Z
dc.date.issued1999en_US
dc.identifier1999-MJ-04en_US
dc.identifier.urihttp://hdl.handle.net/1811/19297
dc.description$^{a}$ W.J. Balfour and R.S. Ram, J. Phys. B 17, L19 (1984). $^{b}$C. Sousa, W.A. de Jong, R. Broer and W.C. Nicuwpoort, Mol. Phys, 92, 677 (1997).en_US
dc.descriptionAuthor Institution: Department of Chemistry, University of Missouri; Department of Chemistry, Southern Illinois Universityen_US
dc.description.abstractThe near infrared electronic transition of CuCl occuring in the region of $13,500 cm^{-1}$ has been recorded by intracavity laser absorption spectroscopy. The CuCl molecules were produced in a copper hollow cathode operating with an applied potential of 700 V, using 1.4 torr argon and a trace amount of carbon tetrachloride. The near infrared transition previously was recorded by Balfour and $Ram,^{a}$ and it was assigned as emission from a low-lying $^{3}\Sigma^{+}$ state to the $X^{1}\Sigma^{+}$ state. Recently, this transition has received considerable attention because of high level ab initio $calculations^{b}$ that question whether this transition involves the $X^{1}\Sigma^{1}$ ground state.en_US
dc.format.extent88323 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleTHE NEAR INFRARED TRANSITION OF COPPER CHLORIDE BY INTRACAVITY LASER SPECTROSCOPYen_US
dc.typearticleen_US


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