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dc.contributor.authorBezrukov, Andrey
dc.contributor.authorTörnroos, Karl Wilhelm
dc.contributor.authorLe Roux, Erwan
dc.contributor.authorDietzel, Pascal D.C.
dc.date.accessioned2024-03-05T08:01:55Z
dc.date.available2024-03-05T08:01:55Z
dc.date.created2019-01-07T12:12:52Z
dc.date.issued2018
dc.identifier.issn1359-7345
dc.identifier.urihttps://hdl.handle.net/11250/3120997
dc.description.abstractTwo zirconium–organic frameworks were synthesized by exchanging the acetate ligands in [Zr12O8(OH)8(CH3COO)24] with polydentate linkers. Partial substitution of acetate groups by a phosphine based linker yielded a new porous framework with this unique dimeric Zr12 cluster unit as molecular building block. More exhaustive substitution of acetate resulted in cleavage of the Zr12 unit and formation of UiO-67.en_US
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleIncorporation of an intact dimeric Zr12 oxo cluster from a molecular precursor in a new zirconium metal-organic frameworken_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionacceptedVersionen_US
dc.rights.holderCopyright The Royal Society of Chemistry 2018en_US
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2
dc.identifier.doi10.1039/c8cc00507a
dc.identifier.cristin1651426
dc.source.journalChemical Communicationsen_US
dc.source.pagenumber2735-2738en_US
dc.identifier.citationChemical Communications. 2018, 54 (22), 2735-2738.en_US
dc.source.volume54en_US
dc.source.issue22en_US


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