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Molecular Beam Measurement of the Hyperfine Structure of 85Rb19F

dc.contributor.authorZorn, Jens C.en_US
dc.contributor.authorEnglish, Thomas C.en_US
dc.contributor.authorDickinson, J. Thomasen_US
dc.contributor.authorStephenson, David A.en_US
dc.date.accessioned2010-05-06T20:14:42Z
dc.date.available2010-05-06T20:14:42Z
dc.date.issued1966-11-15en_US
dc.identifier.citationZorn, Jens C.; English, Thomas C.; Dickinson, J. Thomas; Stephenson, David A. (1966). "Molecular Beam Measurement of the Hyperfine Structure of 85Rb19F." The Journal of Chemical Physics 45(10): 3731-3736. <http://hdl.handle.net/2027.42/69352>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/69352
dc.description.abstractRadio‐frequency transitions between the hfs levels of the J=1 rotational state in 85Rb19F have been observed using a molecular beam electric resonance spectrometer. From these spectra we have obtained values for the constant eq1Q1, which characterizes the interaction between the electric quadrupole moment of the Rb nucleus with the molecular electric‐field gradient; for the constants c1 and c2 which characterize the magnetic interaction between the Rb and F nuclei, respectively, and the rotational angular momentum J of the molecule; and for the constants c3 and c4 which describe the magnetic coupling of the two nuclear spins. Measurements have been made on the first‐five vibrational states. The results for v=0 areeq1Q1=(−70.342±0.001)MHz,c1=(+0.52±0.02)kHz,c2=(+10.615±0.06)kHz,c3=(+0.80±0.06)kHz,c4=(+0.15±0.05)kHz.Values of these constants for v=1, 2, 3, and 4 are given with somewhat less precision.en_US
dc.format.extent3102 bytes
dc.format.extent444107 bytes
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dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleMolecular Beam Measurement of the Hyperfine Structure of 85Rb19Fen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumRandall Laboratory of Physics, The University of Michigan, Ann Arbor, Michiganen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/69352/2/JCPSA6-45-10-3731-1.pdf
dc.identifier.doi10.1063/1.1727393en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
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dc.identifier.citedreferenceWe are grateful to F. Stephenson for assistance with machine computations.en_US
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dc.owningcollnamePhysics, Department of


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