Silicon-catalyzed depolymerization of polyethers: pushing scope, practicability and mechanistic understanding

The depolymerization of polyethers is a sustainable yet challenging opportunity for a circular economy in materials processing. While we recently identified silicon Lewis superacids as promising catalysts for this transformation, limited scope (e. g., terminal OH groups not tolerated) and strict req...

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Main Authors: Ansmann, Nils (Author) , Johann, Kerstin (Author) , Favresse, Philippe (Author) , Johann, Tobias (Author) , Fiedel, Michael (Author) , Greb, Lutz (Author)
Format: Article (Journal)
Language:English
Published: May 2024
In: ChemCatChem
Year: 2024, Volume: 16, Issue: 10, Pages: 1-6
ISSN:1867-3899
DOI:10.1002/cctc.202301615
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/cctc.202301615
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/cctc.202301615
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Author Notes:Nils Ansmann, Kerstin Johann, Philippe Favresse, Tobias Johann, Michael Fiedel, and Lutz Greb
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Summary:The depolymerization of polyethers is a sustainable yet challenging opportunity for a circular economy in materials processing. While we recently identified silicon Lewis superacids as promising catalysts for this transformation, limited scope (e. g., terminal OH groups not tolerated) and strict requirements for anhydrous conditions hampered wider applicability. In the present work, the impact of different polyether structures and reaction conditions were evaluated. By doing so, the generality for structural variations was confirmed and substantial improvements made the depolymerization feasible for large-scale applications under ambient conditions. Based on systematic experimental screenings, a refined mechanistic model of the depolymerization process is developed.
Item Description:Gesehen am 29.05.2024
Physical Description:Online Resource
ISSN:1867-3899
DOI:10.1002/cctc.202301615