Buchumschlag

Aryl- and silyl-substituted silyliumylidene ions in the hydrosilylation of CO2

Tetryliumylidene ions, stabilized by N-heterocyclic carbenes (NHCs), have emerged as promising main-group catalysts for the reduction of carbon dioxide (CO2). Herein, we report the catalytic activity of aryl- and silyl-substituted silyliumylidenes (1 - 4) in the hydrosilylation of CO2 with diphenyls...

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Hauptverfasser: Stigler, Sebastian (VerfasserIn) , Thorwart, Thaddäus (VerfasserIn) , Greb, Lutz (VerfasserIn) , Inoue, Shigeyoshi (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: November 9, 2025
In: ChemCatChem
Year: 2025, Jahrgang: 17, Heft: 23, Pages: 1-6
ISSN:1867-3899
DOI:10.1002/cctc.202501195
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/cctc.202501195
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/cctc.202501195
Volltext
Verfasserangaben:Sebastian Stigler, Thaddäus Thorwart, Lutz Greb, Shigeyoshi Inoue
Beschreibung
Zusammenfassung:Tetryliumylidene ions, stabilized by N-heterocyclic carbenes (NHCs), have emerged as promising main-group catalysts for the reduction of carbon dioxide (CO2). Herein, we report the catalytic activity of aryl- and silyl-substituted silyliumylidenes (1 - 4) in the hydrosilylation of CO2 with diphenylsilane at room temperature, using acetonitrile as solvent. With a low catalyst loading of 5 mol%, full conversion of diphenylsilane was achieved within a moderate reaction time, yielding a mixture of silylformate, bis(silyl)acetal, and silylated methanol. Mechanistic studies, supported by nuclear magnetic resonance (NMR) spectroscopy and density functional theory (DFT) calculations, suggest that the silyliumylidene ions act as precatalysts, forming sila-acylium ion intermediates that subsequently generate the catalytically active siloxy-silylene species. These findings highlight the potential of NHC-stabilized silyliumylidene ions as efficient and selective main-group catalysts for CO2 hydrosilylation.
Beschreibung:Online veröffentlicht: 9. November 2025
Gesehen am 03.02.2026
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Beschreibung:Online Resource
ISSN:1867-3899
DOI:10.1002/cctc.202501195

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