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dc.contributor.authorConrad, Maurice-
dc.contributor.authorRuss, Philip L.-
dc.contributor.authorSchleid, Thomas-
dc.date.accessioned2024-04-30T13:41:35Z-
dc.date.available2024-04-30T13:41:35Z-
dc.date.issued2020de
dc.identifier.issn1521-3749-
dc.identifier.issn0044-2313-
dc.identifier.other1887883533-
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-143271de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/14327-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-14308-
dc.description.abstractColorless single crystals of Sr[ReO4]2 were obtained from halide melts at 1123 K in open corundum crucibles. X‐ray diffraction revealed that Sr[ReO4]2 crystallizes in the monoclinic space group P21/n with the lattice parameters a = 627.31(4) pm, b = 1004.56(7) pm, c = 1271.25(9) pm and β = 97.118(3)° for Z = 4. The crystal structure contains a unique Sr2+‐cation site surrounded by eight crystallographically different oxygen atoms forming distorted bicapped trigonal prisms. All corners of these [SrO8]14- polyhedra (d(Sr-O) = 259-268 pm) are shared with tetrahedral meta‐perrhenate units [ReO4]- (d(Re-O) = 166-173 pm) formed from two crystallographically different Re7+ cations surrounded by four O2- anions each, building up the three‐dimensional mosaic‐like structure of Sr[ReO4]2. Single‐crystal Raman data confirm the presence of two different kinds of symmetry‐free meta‐perrhenate units [ReO4]- and match well with results known from literature.en
dc.description.sponsorshipFederal State of Baden-Württembergde
dc.description.sponsorshipProjekt DEALde
dc.language.isoende
dc.relation.uridoi:10.1002/zaac.202000312de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/de
dc.subject.ddc540de
dc.titleSr[ReO4]2 : the first single crystals of an anhydrous alkaline‐earth metal meta‐perrhenateen
dc.typearticlede
dc.date.updated2023-11-14T05:07:22Z-
ubs.fakultaetChemiede
ubs.institutInstitut für Anorganische Chemiede
ubs.publikation.seiten1872-1875de
ubs.publikation.sourceZeitschrift für anorganische und allgemeine Chemie 646 (2020), S. 1872-1875de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:03 Fakultät Chemie

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