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Electric Dipole Moments of Rare Gas-Carbonyl Sulfide van der Waals Complexes

dc.contributor.authorAndrews A. M. ,en_US
dc.contributor.authorNemes L. ,en_US
dc.contributor.authorMaruca S. L. ,en_US
dc.contributor.authorHillig K. W. ,en_US
dc.contributor.authorKuczkowski R. L. ,en_US
dc.contributor.authorMuenter J. S. ,en_US
dc.date.accessioned2006-04-10T15:39:35Z
dc.date.available2006-04-10T15:39:35Z
dc.date.issued1993-08en_US
dc.identifier.citationAndrews A. M., , Nemes L., , Maruca S. L., , Hillig K. W., , Kuczkowski R. L., , Muenter J. S., (1993/08)."Electric Dipole Moments of Rare Gas-Carbonyl Sulfide van der Waals Complexes." Journal of Molecular Spectroscopy 160(2): 422-433. <http://hdl.handle.net/2027.42/30664>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WK8-45P63SF-2T/2/d29f336da32a092e9239b94112b2468aen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30664
dc.description.abstractThe [mu]a and [mu]b electric dipole moment components of the Ne-OCS, Ar-OCS, and Kr-OCS van der Waals complexes were determined using Fourier transform microwave spectroscopy. The accuracy of these results was evaluated by comparing the Ar-OCS moments with molecular beam electric resonance measurements. The experimental moments are compared with values calculated from projections of the dipole moment of the OCS monomer, corrected for effects from harmonic bending and induced dipole moments in the rare gas atoms. The [mu]a and [mu]b components were reproduced within 0.01 D for the Ar and Kr complexes and within 0.02-0.025 D for the Ne complex.en_US
dc.format.extent616609 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleElectric Dipole Moments of Rare Gas-Carbonyl Sulfide van der Waals Complexesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationotherDepartment of Chemistry, University of Rochester, Rochester, NY 14627, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30664/1/0000307.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1006/jmsp.1993.1189en_US
dc.identifier.sourceJournal of Molecular Spectroscopyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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