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hal.structure.identifierDepartamento de Mineralogía-Petrología, Facultad de Ciencia y Tecnologia
dc.contributor.authorLARRAÑAGA, A.
hal.structure.identifierDepartamento de Química Inorgánica, Facultad de Ciencia y Tecnologia
dc.contributor.authorMESA, José L.
hal.structure.identifierDepartamento de Mineralogía-Petrología, Facultad de Ciencia y Tecnologia
dc.contributor.authorPIZARRO, José L.
hal.structure.identifierDepartamento de Química Inorgánica, Facultad de Ciencia y Tecnologia
dc.contributor.authorPEÑA, A.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorOLAZCUAGA, Roger
hal.structure.identifierDepartamento de Mineralogía-Petrología, Facultad de Ciencia y Tecnologia
dc.contributor.authorARRIORTUA, María I.
hal.structure.identifierDepartamento de Química Inorgánica, Facultad de Ciencia y Tecnologia
dc.contributor.authorROJO, Teófilo
dc.date.issued2005
dc.identifier.issn0022-4596
dc.description.abstractEnTwo new manganese(II) selenite polymorphs with formula Mn(SeO3)·H2O have been synthesized by slow evaporation from an aqueous solution. The crystal structure of both compounds (1) and (2) have been solved from X-ray diffraction data. The structure of (1) was determined from single-crystal X-ray diffraction techniques. The compound crystallizes in the Ama2 space group, with a=5.817(1), b=13.449(3), c=4.8765(9) A and Z=4. The structure of (2) has been solved from X-ray powder diffraction data. This phase crystallizes in the P21/n space group with unit-cell parameters of a=4.921(3), b=13.121(7), c=5.816(1) A, β=90.03(2) and Z=4. Both polymorphs exhibit a layered structure formed by isolated sheets of MnO6 octahedra and (SeO3)2− trigonal pyramids in the (010) plane. These layers, which contain one manganese and selenium atom crystallographically independent, are formed by octahedra linked between them through the selenite oxoanions. The difference of both compounds consists in the stacking of the layers along the b-axis. The IR spectra show the characteristic bands of the selenite anion. Studies of luminescence performed at 6 K and diffuse reflectance spectroscopy have been carried out for both phases. The Dq and Racah (B and C) parameters, from luminescence and diffuse reflectance spectroscopy, are Dq=705, B=750, C=3325 cm-1 for (1) and Dq=720, B=745, C=3350 cm-1 for (2). The ESR spectra of both compounds are isotropic with g-values of 1.99(1). Magnetic measurements indicate the presence of antiferromagnetic couplings in both phases. The J-exchange parameters have been estimated by fitting the experimental magnetic data to a model for square-planar lattice. The values obtained are J/k=-0.83, −0.91 K and J′/k=-0.97, −1.20 K, for polymorphs (1) and (2), respectively.
dc.language.isoen
dc.publisherElsevier
dc.subject.enX-ray diffraction
dc.subject.enSingle-crystal and powder
dc.subject.enIR
dc.subject.enVisible–UV
dc.subject.enLuminiscence
dc.subject.enESR
dc.subject.enMagnetic susceptibility
dc.title.enSynthesis and structural, spectroscopic and magnetic studies of two new polymorphs of Mn(SeO3)·H2O
dc.typeArticle de revue
dc.identifier.doi10.1016/j.jssc.2005.09.034
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Solid State Chemistry
bordeaux.pagep. 3686-3697
bordeaux.volumevo. 178, n° 12
bordeaux.peerReviewedoui
hal.identifierhal-00023489
hal.version1
hal.popularnon
hal.audienceNon spécifiée
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00023489v1
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