Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2637
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dc.contributor.authorYang, Pen_US
dc.contributor.authorLin, Zhengguoen_US
dc.contributor.authorBassil, Bassemen_US
dc.contributor.authorALfaro-Espinoza, Gen_US
dc.contributor.authorUllrich, M.Sen_US
dc.contributor.authorLi, M.Xen_US
dc.contributor.authorSilvestru, Cen_US
dc.contributor.authorKortz, Ulrichen_US
dc.date.accessioned2020-12-23T09:17:22Z-
dc.date.available2020-12-23T09:17:22Z-
dc.date.issued2016-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2637-
dc.description.abstractTwo tetra-antimony(III)-bridged, sandwich-type 18-tungsto-2-arsenates(V), [(LSb(III))4(A-α-As(V)W9O34)2](10-) (L = Ph (1), OH (2)), were prepared and fully characterized in the solid state and in solution. Both polyanions are stable in aqueous physiological medium for at least 24 h (at concentrations ≥2.5 × 10(-6) M). Despite the presence of an isostructural tetra-antimony(III) motif in 1 and 2, distinctly different antibacterial activity was observed for both polyanions. The minimum inhibitory concentrations (MIC) of 1 (7.8-62.5 μg/mL) is lower than for any other organoantimony(III)-containing polyoxometalate reported to date.en_US
dc.format.extent2 p.en_US
dc.language.isoengen_US
dc.titleTetra-antimony(III)-bridged 18-tungsto-2-arsenates(V), [(LSb(III))4(A-α-As(V)W9O34)2](10-) (L = Ph, OH): turning bioactivity on and off by ligand substitutionen_US
dc.typeJournal Articleen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume55en_US
dc.description.startpage3718en_US
dc.description.endpage3720en_US
dc.date.catalogued2017-11-17-
dc.description.statusPublisheden_US
dc.identifier.OlibID175049-
dc.relation.ispartoftextJournal of inorganic chemistryen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Chemistry
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