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

Citation
G. Vanhoyland et al., Structure determination and refinement of acid strontium oxalate from X-ray and neutron powder diffraction, J SOL ST CH, 157(2), 2001, pp. 283-288
Citations number
14
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF SOLID STATE CHEMISTRY
ISSN journal
00224596 → ACNP
Volume
157
Issue
2
Year of publication
2001
Pages
283 - 288
Database
ISI
SICI code
0022-4596(200103)157:2<283:SDAROA>2.0.ZU;2-X
Abstract
The structure of acid strontium oxalate Sr(HC2O4) . 1/2(C2O4) . H2O has bee n determined by conventional X-ray powder diffractometry, The diffraction p attern was indexed from a monoclinic unit cell with cell parameters a = 6.3 41(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 trigona l 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 classific ation (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.