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Energy Levels and Thermodynamic Properties of the Internal Rotator

dc.contributor.authorHalford, J. O.en_US
dc.date.accessioned2010-05-06T21:44:03Z
dc.date.available2010-05-06T21:44:03Z
dc.date.issued1950-04en_US
dc.identifier.citationHalford, J. O. (1950). "Energy Levels and Thermodynamic Properties of the Internal Rotator." The Journal of Chemical Physics 18(4): 444-448. <http://hdl.handle.net/2027.42/70165>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/70165
dc.description.abstractTo facilitate the calculation of the thermodynamic properties of internal rotators lying outside the limits of available tabulations, methods of determining the energy levels are studied for the purpose of finding the most expeditious route to accurate results. It proves to be unnecessary in any case to calculate many levels from the wave mechanics. A partition function is set up in terms of the correct ground state and a series of approximate levels derived from the old quantum theory, and this is corrected to constancy by the successive substitution of correct levels, starting with the first excited state. A set of levels obtained in this way which gives the correct partition function always leads to correct values of all the thermodynamic properties.To obtain accurate energy levels, the continued fractions of Koehler and Dennison are recommended as most convenient.en_US
dc.format.extent3102 bytes
dc.format.extent370706 bytes
dc.format.mimetypetext/plain
dc.format.mimetypeapplication/pdf
dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleEnergy Levels and Thermodynamic Properties of the Internal Rotatoren_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumChemistry Department, University of Michigan, Ann Arbor, Michiganen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/70165/2/JCPSA6-18-4-444-1.pdf
dc.identifier.doi10.1063/1.1747659en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
dc.identifier.citedreferenceK. S. Pitzer and W. D. Gwinn, J. Chem. Phys. 10, 428 (1942).en_US
dc.identifier.citedreferenceD. G. Burkhard and D. M. Dennison, private communication.en_US
dc.identifier.citedreferenceHill, Whittaker, and Watson, Modern Analysis (Cambridge University Press, London, 1935), p. 413.en_US
dc.identifier.citedreferenceJ. S. Koehler and D. M. Dennison, Phys. Rev. 57, 1006 (1940).en_US
dc.identifier.citedreferenceJ. O. Halford, J. Chem. Phys. 15, 645 (1947).en_US
dc.identifier.citedreferenceJ. O. Halford, J. Chem. Phys. 16, 410 (1948), Table II.en_US
dc.owningcollnamePhysics, Department of


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