Cyclic water hexamers and decamers in a porous lanthanide-organic framework: Correlation between some physical properties and crystal structure

dc.contributor.authorMichaelides, A.en
dc.contributor.authorSkoulika, S.en
dc.contributor.authorBakalbassis, E. G.en
dc.contributor.authorMrozinski, J.en
dc.date.accessioned2015-11-24T16:55:11Z
dc.date.available2015-11-24T16:55:11Z
dc.identifier.issn1528-7483-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/10270
dc.rightsDefault Licence-
dc.subjectsecondary building unitsen
dc.subjectcoordination polymersen
dc.subjectmagnetic-propertiesen
dc.subjectchemistryen
dc.subjectclustersen
dc.subjectcomplexen
dc.subjectsolidsen
dc.subjectcontractionen
dc.subjectnetworken
dc.subjecthydrateen
dc.titleCyclic water hexamers and decamers in a porous lanthanide-organic framework: Correlation between some physical properties and crystal structureen
heal.abstractErbium. fumarate [Er-2(fum)(3)(H2O)(4)].8H(2)O, 1, (fum = fumarate dianion) crystallizes at room temperature in a silica gel column. The structure is three-dimensional and consists of layers of erbium fumarate pillared by fumarate dianions acting in the bis-chelating mode. The layers contain arrays of erbium cations bridged by fumarate dianions acting in the bis-bidentate bridging mode. The relatively large channels formed in the direction of the a and c axes are filled by water molecules that form a hydrogen bonded layer, comprising cyclic hexamers with both boat and chair conformations and cyclic decamers with boat-chair-boat conformation. The water molecules are reversibly removed at 90 degreesC. The evacuated metal-organic framework, 2, is stable up to 400 degreesC. Both compounds 1 and 2 exhibit weak antiferromagnetic interactions.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1021/Cg034025w-
heal.identifier.secondary<Go to ISI>://000183960200008-
heal.identifier.secondaryhttp://pubs.acs.org/doi/abs/10.1021/cg034025w-
heal.journalNameCrystal Growth & Designen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2003-
heal.publisherAmerican Chemical Societyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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