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dc.creatorAVILA, M.-
dc.creatorREGUERA, L.-
dc.creatorVARGAS, C.-
dc.creatorREGUERA, E.-
dc.date2012-03-27T00:32:12Z-
dc.date2012-03-27T00:32:12Z-
dc.date2008-12-01-
dc.date.accessioned2013-01-16T11:37:26Z-
dc.date.available2013-01-16T11:37:26Z-
dc.date.issued2013-01-16-
dc.identifierJournal ofPhysicsandChemistryofSolids70(2009)477–482-
dc.identifierhttp://hdl.handle.net/123456789/498-
dc.identifier.urihttp://www.repositoriodigital.ipn.mx/handle/123456789/10986-
dc.descriptionZinc hexacyanoruthenate(II)andhexacyanoosmate(II)werepreparedandstudiedfromX-ray diffraction (XRD),infrared(IR),andthermogravimetric(TG)data.Thesecompoundswerefoundtobe isomorphouswiththeironanalogues,crystallizingwitharhombohedralunitcell(R 3c spacegroup), where thezincatomhastetrahedralcoordinationtoNendsofCNgroups.ForCs,compoundswith formulaunitZnCs2[M(CN)6] andacubicunitcell(Fm 3m) werealsoobtained.Thecrystalstructures for theeightcompositionswererefinedfromthecorrespondingX-raypowderdiffractionpatternsusing the Rietveldmethod.RelatedtothetetrahedralcoordinationfortheZnatom,therhombohedralphase has aporousframeworkwithellipsoidalcavitiesofabout12.5 9 8A˚ , communicatedbyelliptical windowsof 5A˚ . Withinthesecavitiestheexchangeablealkalimetalionsarefound.Thefillingofthe cavityvolumeiscompletedwithwatermolecules.IRspectrumsensescertainchargedelocalization from theinnermetal,throughthe p-back donationmechanism.ForOscompoundsthiseffectis particularlypronounced,relatedtoamorediffusedorbitalsforthismetal. & 2008ElsevierLtd.Allrightsreserved-
dc.languageen-
dc.publisherJournal ofPhysicsandChemistryofSolids-
dc.subjectInorganiccompounds-
dc.subjectMicroporousmaterials-
dc.subjectX-raydiffraction-
dc.subjectCrystalstructure-
dc.titleTetrahedralcoordinationforZninhexacyanometallates:Structuresof Zn3A2[M(CN)6]2 xH2O withA ¼ K, Rb,CsandM ¼ Ru,Os-
dc.typeArticle-
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