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Título: | Structure of magnesium selenate enneahydrate, MgSeO4·9H2O, from 5 to 250K using neutron time-of-flight Laue diffraction |
Autor: | Fortes, Andrew D.; Alfè, D.; Hernández, Eduardo R. CSIC ORCID; Gutmann, M. J. | Palabras clave: | Dodecamer Neutron diffraction Magnesium selenate enneahydrate |
Fecha de publicación: | 2015 | Editor: | International Union of Crystallography | Citación: | Acta Crystallographica - Section B - Structural Science 71: 313-327 (2015) | Resumen: | The complete structure of MgSeO4·9H2O has been refined from neutron single-crystal diffraction data obtained at 5, 100, 175 and 250 K. It is monoclinic, space group P21/c, Z = 4, with unit-cell parameters a = 7.222 (2), b = 10.484 (3), c = 17.327 (4) Å, [beta] = 109.57 (2)°, and V = 1236.1 (6) Å3 [[rho]calc = 1770 (1) kg m-3] at 5 K. The structure consists of isolated [Mg(H2O)6]2+ octahedra, [SeO4]2- tetrahedra and three interstitial lattice water molecules, all on sites of symmetry 1. The positions of the H atoms agree well with those inferred on the basis of geometrical considerations in the prior X-ray powder diffraction structure determination: no evidence of orientational disorder of the water molecules is apparent in the temperature range studied. Six of the nine water molecules are hydrogen bonded to one another to form a unique centrosymmetric dodecamer, (H2O)12. Raman spectra have been acquired in the range 170-4000 cm-1 at 259 and 78 K; ab initio calculations, using density functional theory, have been carried out in order to aid in the analysis of the Raman spectrum as well as providing additional insights into the geometry and thermodynamics of the hydrogen bonds. Complementary information concerning the thermal expansion, crystal morphology and the solubility are also presented. | Versión del editor: | http://doi.org/10.1107/S2052520615006824 | URI: | http://hdl.handle.net/10261/182797 | DOI: | 10.1107/S2052520615006824 | Identificadores: | doi: 10.1107/S2052520615006824 e-issn: 2052-5206 issn: 2052-5192 |
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