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Crystal Structure Refinement of SrMoO4, SrWO4, CaMoO4, and BaWO4 by Neutron Diffraction
dc.contributor.authorGürmen, Erdoganen_US
dc.contributor.authorDaniels, Eugeneen_US
dc.contributor.authorKing, John Swintonen_US
dc.date.accessioned2010-05-06T22:03:23Z
dc.date.available2010-05-06T22:03:23Z
dc.date.issued1971-08-01en_US
dc.identifier.citationGürmen, Erdogan; Daniels, Eugene; King, J. S. (1971). "Crystal Structure Refinement of SrMoO4, SrWO4, CaMoO4, and BaWO4 by Neutron Diffraction." The Journal of Chemical Physics 55(3): 1093-1097. <http://hdl.handle.net/2027.42/70371>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/70371
dc.description.abstractThe crystal structures of CaMoO4, SrMoO4, SrWO4, and BaWO4 have been refined from neutron diffraction data taken in the (h0l)(h0l) and (hhl)(hhl) zones. Oxygen position refinement is started from the parameters proposed by Sillén and Nylander and results in an improvement of over an order of magnitude in the oxygen coordinates. A comparison of coordinates for the different compounds shows several systematic differences.en_US
dc.format.extent3102 bytes
dc.format.extent244239 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.titleCrystal Structure Refinement of SrMoO4, SrWO4, CaMoO4, and BaWO4 by Neutron Diffractionen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Nuclear Engineering, The University of Michigan, Ann Arbor, Michigan 48104en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/70371/2/JCPSA6-55-3-1093-1.pdf
dc.identifier.doi10.1063/1.1676191en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
dc.identifier.citedreferenceL. G. Sillén and A. L. Nylander, Arkiv Kemi Miner. Geol. 17A, 4 (1943).en_US
dc.identifier.citedreferenceA. Zalkin and D. H. Templeton, J. Chem. Phys. 40, 501 (1964).en_US
dc.identifier.citedreferenceM. I. Kay, B. C. Frazer, and I. Almodovar, J. Chem. Phys. 40, 504 (1964).en_US
dc.identifier.citedreferenceJ. Leciejewicz, Z. Krist. 121, 158 (1965). The coordinates of Table II have been transformed to correspond to O0O0 in the Sillén and Nylander notation.en_US
dc.identifier.citedreferenceInternational Tables for X‐Ray Crystallography (The International Union of Crystallography, Birmingham, England, 1952), Vol. 1.en_US
dc.identifier.citedreferenceNatl. Bur. Std. (U.S.) Monograph 25, (1962).en_US
dc.identifier.citedreferenceW. R. Busing, K. O. Martin, and H. A. Levy, ORNL‐TM‐305, 1962.en_US
dc.identifier.citedreferenceThe scattering length for Sr has recently been revised to 0.683×0.10−12 cm0.683×0.10−12cm by B. O. Loopstra and H. M. Rietveld, Acta Cryst. B25, 787 (1969).en_US
dc.identifier.citedreferenceThe addition of a torsional correction of 0.003 Å to the O0‐X1O0‐X1 bond length in Ref. 3 has not been made for our results.en_US
dc.identifier.citedreferenceL. Pauling, Nature of the Chemical Bond (Cornell U.P., Ithaca, N.Y., 1960), p. 518.en_US
dc.identifier.citedreferenceV. M. Goldschmidt, Skrifter Norske Videnskaps‐Akad Oslo, I. Mat. Naturv. Kl. 1926, 1.en_US
dc.identifier.citedreferenceR. W. G. Wyckoff, Crystal Structures (Wiley, New York, 1965), 2nd ed., Vol. 1.en_US
dc.owningcollnamePhysics, Department of


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