Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-9720
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dc.contributor.authorRepp, Stefan-
dc.contributor.authorRemmers, Moritz-
dc.contributor.authorRein, Alexandra Stefanie Jessica-
dc.contributor.authorSorsche, Dieter-
dc.contributor.authorGao, Dandan-
dc.contributor.authorAnjass, Montaha-
dc.contributor.authorMondeshki, Mihail-
dc.contributor.authorCarrella, Luca M.-
dc.contributor.authorRentschler, Eva-
dc.contributor.authorStreb, Carsten-
dc.date.accessioned2023-11-29T14:39:42Z-
dc.date.available2023-11-29T14:39:42Z-
dc.date.issued2023-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/9738-
dc.description.abstractThe introduction of metal sites into molecular metal oxides, so-called polyoxometalates, is key for tuning their structure and reactivity. The complex mechanisms which govern metal-functionalization of polyoxometalates are still poorly understood. Here, we report a coupled set of light-dependent and light-independent reaction equilibria controlling the mono- and di-metal-functionalization of a prototype molecular vanadium oxide cluster. Comprehensive mechanistic analyses show that coordination of a Mg2+ ion to the species {(NMe2H2)2[VV12O32Cl]}3- results in formation of the mono-functionalized {(NMe2H2)[(MgCl)VV12O32Cl]}3- with simultaneous release of a NMe2H2+ placeholder cation. Irradiation of this species with visible light results in one-electron reduction of the vanadate, exchange of the second NMe2H2+ with Mg2+, and formation/crystallization of the di-metal-functionalized [(MgCl)2VIVVV11O32Cl]4-. Mechanistic studies show how stimuli such as light or competing cations affect the coupled equilibria. Transfer of this synthetic concept to other metal cations is also demonstrated, highlighting the versatility of the approach.en_GB
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleCoupled reaction equilibria enable the light-driven formation of metal-functionalized molecular vanadium oxidesen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-9720-
jgu.type.contenttypeScientific articlede
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleNature Communicationsde
jgu.journal.volume14de
jgu.pages.alternative5563de
jgu.publisher.year2023-
jgu.publisher.nameSpringer Naturede
jgu.publisher.placeLondonde
jgu.publisher.issn2041-1723de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1038/s41467-023-41257-yde
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.subject.dfgNaturwissenschaftende
Appears in collections:DFG-491381577-G

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