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dc.creatorJungen, Ch.en_US
dc.date.accessioned2006-06-15T16:47:11Z
dc.date.available2006-06-15T16:47:11Z
dc.date.issued1968en_US
dc.identifier1968-Sigma-10en_US
dc.identifier.urihttp://hdl.handle.net/1811/15576
dc.descriptionAuthor Institution: Division of Pure Physics, National Research Council of Canadaen_US
dc.description.abstractThe rotational structure of the $4f-X^{2}II$ bands in the absorption spectrum of NO has been studied. In contrast to the structure of the 3d and 4d complexes wherein only partial l-coupling of the Rydberg electron $(l=2)$ was found comprising only $\lambda=0$ and 1, the 4f complex shows total uncoupling for all $\lambda \leq 3$ and case d is approached for very low rotation. The band structure, therefore, is of a very unusual type and is characterized by anomalous intensities. The magnitudes of the coupling of l to the rotational axis and of the spin orbit interaction appear directly in the spectrum as intervals between conspicuous heads of the band.en_US
dc.format.extent104710 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleROTATIONAL STRUCTURE OF THE 4f ABSORPTION BAND OF THE NO MOLECULEen_US
dc.typearticleen_US


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