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dc.creatorMARTINEZ GARCIA, R.-
dc.creatorREGUERA, E.-
dc.creatorBALMASEDA, J.-
dc.date2012-03-29T02:06:09Z-
dc.date2012-03-29T02:06:09Z-
dc.date2004-03-29-
dc.date.accessioned2013-01-16T16:02:57Z-
dc.date.available2013-01-16T16:02:57Z-
dc.date.issued2013-01-16-
dc.identifierPowder Diffraction 19 (3), September 2004-
dc.identifierhttp://hdl.handle.net/123456789/1087-
dc.identifier.urihttp://www.repositoriodigital.ipn.mx/handle/123456789/11533-
dc.descriptionThe crystal structures of some nickel hexacyanoferrates ~II, III!, including mixed compositions containing Na1, K1 and Cs1, were resolved and refined from XRD powder patterns. Data from infrared, Mo¨ssbauer and adsorption techniques provided complementary structural information. The crystal structures of Ni3@Fe(CN)6#2 16H2O and NiCs2@Fe(CN)6# were refined in space group Fm3m. NiNa2@Fe(CN)6# 2H2O and NiK2@Fe(CN)6# 2H2O were found to be orthorhombic ~space group Pmn21). This structure (Pmn21) results from a distortion around the alkali ion, which appears as a monohydrated interstitial species. On ionic exchange in an aqueous solution containing Cs1, the orthorhombic distortion disappears and the cubic cell is obtained. Cs1 is a large cation and space is not available for interstitial water molecules. This orthorhombic model is also supported by the Mo¨ssbauer spectra of the ferrous analogs, FeK2@Fe(CN)6# xH2O and Fe@Pt(CN)6#. © 2004 International Centre for Diffraction Data. @DOI: 10.1154/1.1757448#-
dc.languageen-
dc.publisherInternational Centre for Diffraction-
dc.subjectnickel hexacyanoferrates ~II,III!-
dc.subjectRietveld-
dc.subjectcrystal structure-
dc.subjectferrocyanide-
dc.subjectferricyanide-
dc.titleOn the crystal structures of some nickel hexacyanoferrates II,III-
dc.typeArticle-
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