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dc.creatorLEMUS-SANTANA, ANA ADELA-
dc.creatorRODRIGUEZ-HERNANDEZ, JOELIS-
dc.creatorDEL CASTILLO, LUIS FELIPE-
dc.creatorBASTERRECHEA, MARIO-
dc.creatorREGUERA, EDILSO-
dc.date2012-03-18T03:32:22Z-
dc.date2012-03-18T03:32:22Z-
dc.date2009-01-08-
dc.date.accessioned2013-01-16T09:11:48Z-
dc.date.available2013-01-16T09:11:48Z-
dc.date.issued2013-01-16-
dc.identifierJ SOLID STATE CHEM 182 (2009) 757-766-
dc.identifier0022-4596-
dc.identifierhttp://hdl.handle.net/123456789/182-
dc.identifier.urihttp://www.repositoriodigital.ipn.mx/handle/123456789/10699-
dc.descriptionThe materials under study, T[Ni(CN)4]·2pyz with T = Mn, Zn, Cd, were prepared by separation of T[Ni(CN)4] layers in citrate aqueous solution to allow the intercalation of the pyrazine molecules. The obtained solids were characterized from chemical analyses, X-ray diffraction, infrared,Raman, thermogravimetry, UV–Vis,magnetic and adsorption data.Their crystal structure was solved from ab initio using direct methods and then refined by the Rietveld method. A unique coordination for pyrazine to metal centers at neighboring layers was observed. The pyrazine molecule is found forming a bridge between Ni and T atoms, quite different from the proposed structures for T = Fe, Ni where it remains coordinated to two T atoms to form a vertical pillar between neighboring layers. The coordination of pyrazine to both Ni and T atoms minimizes the material free volume and leads to form a hydrophobic framework. On heating the solids remain stable up to140 ºC. No CO2 and H2 adsorption was observed in the small free spaces of their frameworks.-
dc.languageen-
dc.publisherELSEVIER-
dc.subjectLayered compounds-
dc.subjectPillared solids-
dc.titleUnique coordination of pyrazine in T[Ni(CN)4]· 2pyzwith T = Mn, Zn,Cd-
dc.typeArticle-
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