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dc.creatorGaines, Lindaen_US
dc.creatorTomasevich, G. R.en_US
dc.date.accessioned2006-06-15T13:40:04Z
dc.date.available2006-06-15T13:40:04Z
dc.date.issued1975en_US
dc.identifier1975-Sigma-11en_US
dc.identifier.urihttp://hdl.handle.net/1811/9408
dc.descriptionPresent address of Linda Gaines: University of Chicago, Department of Chemistry, 5735 South Ellis Avenue, Chicago, Illinois, 60637.""en_US
dc.descriptionAuthor Institution: Columbia Radiation Laboratory, Columbia Universityen_US
dc.description.abstractSeveral rotational transitions in the frequency range from 1.9-4.5 GHz of the similar organic ring molecules pyrrole, $C_{4}H_{5}N$, and pyridine, $C_{5}H_{5}N$, have been studied in a beam maser spectrometer with a resolution of better than 1KHz. The complex hyperfine structure resulting from the six interacting spins has been resolved and analyzed, yielding the diagonal elements of the quadrupole and spin rotation tensors for bath molecules. For pyrrole, an electron-coupled spin-spin interaction of about 1KHz was added in order to fit the theoretical to experimental spectra. Results are compared with those, for a third similar ring molecule, furan, $C_{4}H_{4}O$, previously studied in this laboratory.en_US
dc.format.extent108891 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleBEAM MASER SPECTROSCOPY OF PYRROLE AND PYRiDINEen_US
dc.typearticleen_US


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