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Elsevier, Journal of Solid State Chemistry, 2(157), p. 283-288

DOI: 10.1006/jssc.2000.9057

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Structure determination and refinement of acid strontium oxalate from X-ray and neutron powder diffraction

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

The structure of acid strontium oxalate Sr(HC2O4) . 1/2(C2O4) . H2O has been determined by conventional X-ray powder diffractometry, The diffraction pattern was indexed from a monoclinic unit cell with cell parameters a = 6.341(1) Angstrom, b = 16.880(2) Angstrom, c = 5.7798(8) Angstrom, and beta = 97.60(1)degrees; space group, P2(1)/n (No. 14) with Z = 4. Final (isotropic) Rietveld refinement of the neutron powder data yielded R-B = 4.57%, R-F = 2.87%, and R-WP = 7.87% as conventional Rietveld parameters. Strontium is eight-fold coordinated and can be described as a distorted bicapped trigonal prism. The SrO8 polyhedra form one-dimensional chains along the c-axis bf sharing edges, In contrast to all other known strontium oxalates, in this compound H2O acts as bridging ligand between two Sr atoms, SDPD-D classification (1): Sr(HC2O4)-1/2(C2O4)-H2O, P2(1)/n, C1=14, Nc = 42, C2 = 11, XC1 + N/TREOR-97 & DICVOL-91, EXTRA, EQUI, SIRPOW-92 (DM), GFOURIER, FULLPROF, (C) 2001 Academic Press.