Polyoxometalate aerogels formed by organofunctionalized Anderson polyoxometalates as low molecular weight gelators

dc.contributor.authorSachdeva, Garima
dc.contributor.authorMaloul, Salam
dc.contributor.authorZolg, Julia
dc.contributor.authorMüller, Riccarda
dc.contributor.authorMondeshki, Mihail
dc.contributor.authorEbrahimi, Elnaz
dc.contributor.authorAbid, Dhouha
dc.contributor.authorChala, Soressa Abera
dc.contributor.authorNeumann, Christof
dc.contributor.authorTurchanin, Andrey
dc.contributor.authorBiskupek, Johannes
dc.contributor.authorKaiser, Ute
dc.contributor.authorLeopold, Kerstin
dc.contributor.authorStreb, Carsten
dc.date.accessioned2025-12-02T14:38:02Z
dc.date.issued2025
dc.description.abstractPolyoxometalate-based aerogels, built through supramolecular interactions and metal coordination, have the potential to expand the field of smart materials. Here, the first example of the conversion of an Anderson-polyoxometalate-based organogel into a catalytically active aerogel is reported. The polyoxometalate organogel is formed by the reaction of ZnCl2 with the TRIS-functionalized Anderson polyoxometalate (nBu4N)3[MnMo6O18{(OCH2)3CNH2}2]. Conversion of the organogel into the aerogel is achieved by a scalable freeze-drying procedure. A range of experimental methods are employed to follow the conversion of the POM into the organogel and aerogel, and insights into the role of the polyoxometalate, the metal salt, and the solvent are reported. The catalytic activity of the aerogel for selective alcohol oxidations (model compounds: benzyl alcohol, furfuryl alcohol, octanol) is reported together with initial recyclability studies. A conversion yield of 30% for benzaldehyde is achieved using aerogel as a catalyst. The study opens the door to (multi-)functional polyoxometalate-based aerogels for sorption, separation, catalysis, and energy technologies.en_GB
dc.identifier.doihttps://doi.org/10.25358/openscience-13775
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/13796
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titlePolyoxometalate aerogels formed by organofunctionalized Anderson polyoxometalates as low molecular weight gelatorsen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.netprice2080,00
jgu.apc.price2225,60
jgu.apc.taxrate7
jgu.apc.transformationcontractWiley (DEAL)
jgu.dfg.year2025
jgu.identifier.uuida43f21d1-eece-4cf0-883e-64766c8ccc1f
jgu.journal.issue22
jgu.journal.titleAdvanced materials interfaces
jgu.journal.volume12
jgu.nationalcurrency.eur2080,00
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativee00597
jgu.publisher.doi10.1002/admi.202500597
jgu.publisher.eissn2196-7350
jgu.publisher.nameWiley-VCH
jgu.publisher.placeWeinheim
jgu.publisher.year2025
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode540
jgu.subject.dfgNaturwissenschaftende_DE
jgu.type.contenttypeScientific articleen_GB
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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