Electron Densities from Gas‐Phase Electron Diffraction Intensities. II. Molecular Hartree–Fock Cross Sections
dc.contributor.author | Kohl, D. A. | en_US |
dc.contributor.author | Bartell, Lawrence S. | en_US |
dc.date.accessioned | 2010-05-06T21:41:20Z | |
dc.date.available | 2010-05-06T21:41:20Z | |
dc.date.issued | 1969-10-01 | en_US |
dc.identifier.citation | Kohl, D. A.; Bartell, L. S. (1969). "Electron Densities from Gas‐Phase Electron Diffraction Intensities. II. Molecular Hartree–Fock Cross Sections." The Journal of Chemical Physics 51(7): 2896-2904. <http://hdl.handle.net/2027.42/70136> | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/70136 | |
dc.description.abstract | Differential cross sections for electron scattering based on molecular Hartree–Fock electron densities are compared with cross sections based on the independent‐atom approximation for the molecules C2, N2, O2, F2, and CO. The results show that bonding effects on the electron density manifest themselves to the extent of several percent in the scattered intensity at small scattering angles. Furthermore, molecule‐to‐molecule variations in the shifts of electron density are clearly reflected in variations in the functional form of the scattered intensity. A comparison of the calculated intensities for N2 and O2 with preliminary experimental intensities suggests that electron scattering techniques now in development should be able to provide information about bonding and electron correlation effects competitive in accuracy with that of current quantum‐mechanical calculations. | en_US |
dc.format.extent | 3102 bytes | |
dc.format.extent | 580800 bytes | |
dc.format.mimetype | text/plain | |
dc.format.mimetype | application/pdf | |
dc.publisher | The American Institute of Physics | en_US |
dc.rights | © The American Institute of Physics | en_US |
dc.title | Electron Densities from Gas‐Phase Electron Diffraction Intensities. II. Molecular Hartree–Fock Cross Sections | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Physics | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Chemistry and Institute of Science and Technology, The University of Michigan, Ann Arbor, Michigan 48104 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/70136/2/JCPSA6-51-7-2896-1.pdf | |
dc.identifier.doi | 10.1063/1.1672430 | en_US |
dc.identifier.source | The Journal of Chemical Physics | en_US |
dc.identifier.citedreference | D. A. Kohl and L. S. Bartell, J. Chem. Phys. 51, 2891 (1969), Paper I. | en_US |
dc.identifier.citedreference | R. A. Bonham, J. Phys. Chem. 71, 856 (1967). | en_US |
dc.identifier.citedreference | M. Roux, S. Besnainou, and R. Daudel, J. Chim. Phys. 54, 218 (1956); M. Roux, M. Cornille, and L. Burnelle, J. Chem. Phys. 37, 933 (1962). | en_US |
dc.identifier.citedreference | R. F. W. Bader, W. H. Henneker, and Paul E. Cade, J. Chem. Phys. 46, 3341 (1967). | en_US |
dc.identifier.citedreference | T. G. Strand, D. A. Kohl, and R. A. Bonham, J. Chem. Phys. 39, 1307 (1963). | en_US |
dc.identifier.citedreference | L. S. Bartell and R. M. Gavin, Jr., J. Am. Chem. Soc. 86, 3493 (1964); J. Chem. Phys. 43, 856 (1965); R. M. Gavin, Jr. and L. S. Bartell, 44, 3687 (1966); 45, 4700 (1966). | en_US |
dc.identifier.citedreference | D. A. Kohl and R. A. Bonham, J. Chem. Phys. 47, 1634 (1967). | en_US |
dc.identifier.citedreference | M. Abramowitz and I. A. Stegun, Handbook of Mathematical Functions (U.S. Government Printing Office, Washington, D.C., 1965), Eq. 10.1.47, p. 440. | en_US |
dc.identifier.citedreference | A. Erdelyi et al., Tables of Integral Transforms (McGraw‐Hill Book Co., New York, 1954), Vol. 2, p. 280. | en_US |
dc.identifier.citedreference | H. L. Cox, Jr. and R. A. Bonham, J. Chem. Phys. 47, 2599 (1967). | en_US |
dc.owningcollname | Physics, Department of |
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