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http://dx.doi.org/10.18419/opus-14205
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DC Element | Wert | Sprache |
---|---|---|
dc.contributor.author | Beurer, Ann‐Katrin | - |
dc.contributor.author | Kirchhof, Manuel | - |
dc.contributor.author | Bruckner, Johanna R. | - |
dc.contributor.author | Frey, Wolfgang | - |
dc.contributor.author | Baro, Angelika | - |
dc.contributor.author | Dyballa, Michael | - |
dc.contributor.author | Giesselmann, Frank | - |
dc.contributor.author | Laschat, Sabine | - |
dc.contributor.author | Traa, Yvonne | - |
dc.date.accessioned | 2024-04-12T09:32:16Z | - |
dc.date.available | 2024-04-12T09:32:16Z | - |
dc.date.issued | 2021 | de |
dc.identifier.issn | 1867-3899 | - |
dc.identifier.issn | 1867-3880 | - |
dc.identifier.other | 188611644X | - |
dc.identifier.uri | http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-142245 | de |
dc.identifier.uri | http://elib.uni-stuttgart.de/handle/11682/14224 | - |
dc.identifier.uri | http://dx.doi.org/10.18419/opus-14205 | - |
dc.description.abstract | Selectively functionalized mesoporous silica may considerably advance heterogeneous catalysis through the controlled immobilization of highly selective complex catalysts inside the mesopores. However, spatially controlled functionalization and the precise analytical verification are still a challenge. In this publication, we report a method, which ensures a selective functionalization of the mesopore surface with a clickable linker and thus makes it possible to study confinement effects during catalyzed reactions. First, we passivate the silanol groups on the particle surface and in the pore entrances of the mesoporous silica material SBA‐15 with 1,1,1‐trimethyl‐N‐(trimethylsilyl)silanamine. Then we remove the template by solvent extraction and functionalize the pore walls with 3‐azidopropyltriethoxysilane before we click the catalyst. In initial experiments of asymmetric Rh‐catalyzed 1,2‐addition, we investigate the performance of a catalyst clicked selectively in the mesopores and compare it to the dissolved catalyst as well as to the catalyst immobilized exclusively on the external surface of SBA‐15. | en |
dc.description.sponsorship | Deutsche Forschungsgemeinschaft | de |
dc.description.sponsorship | Projekt DEAL | de |
dc.language.iso | en | de |
dc.relation.uri | doi:10.1002/cctc.202100229 | de |
dc.rights | info:eu-repo/semantics/openAccess | de |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | de |
dc.subject.ddc | 540 | de |
dc.title | Efficient and spatially controlled functionalization of SBA‐15 and initial results in asymmetric Rh‐catalyzed 1,2‐additions under confinement | en |
dc.type | article | de |
dc.date.updated | 2023-11-14T04:26:07Z | - |
ubs.fakultaet | Chemie | de |
ubs.institut | Institut für Organische Chemie | de |
ubs.institut | Institut für Physikalische Chemie | de |
ubs.institut | Institut für Technische Chemie | de |
ubs.publikation.seiten | 2407-2419 | de |
ubs.publikation.source | ChemCatChem 13 (2021), S. 2407-2419 | de |
ubs.publikation.typ | Zeitschriftenartikel | de |
Enthalten in den Sammlungen: | 03 Fakultät Chemie |
Dateien zu dieser Ressource:
Datei | Beschreibung | Größe | Format | |
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CCTC_CCTC202100229.pdf | 4,78 MB | Adobe PDF | Öffnen/Anzeigen |
Diese Ressource wurde unter folgender Copyright-Bestimmung veröffentlicht: Lizenz von Creative Commons