Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water

Using water as a monomer in polymerization reactions presents a unique and exquisite strategy towards more sustainable chemistry. Herein, the feasibility thereof is demonstrated by the introduction of the oxa-Michael polyaddition of water and divinyl sulfone. Upon nucleophilic or base catalysis, the...

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Published inChemical science (Cambridge) Vol. 13; no. 23; pp. 692 - 6928
Main Authors Ratzenböck, Karin, Ud Din, Mir Mehraj, Fischer, Susanne M, agar, Ema, Pahovnik, David, Boese, A. Daniel, Rettenwander, Daniel, Slugovc, Christian
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 15.06.2022
The Royal Society of Chemistry
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Summary:Using water as a monomer in polymerization reactions presents a unique and exquisite strategy towards more sustainable chemistry. Herein, the feasibility thereof is demonstrated by the introduction of the oxa-Michael polyaddition of water and divinyl sulfone. Upon nucleophilic or base catalysis, the corresponding aliphatic polyethersulfone is obtained in an interfacial polymerization at room temperature in high yield (>97%) within an hour. The polyethersulfone is characterized by relatively high molar mass averages and a dispersity around 2.5. The polymer was tested as a solid polymer electrolyte with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as the salt. Free-standing amorphous membranes were prepared by a melt process in a solvent-free manner. The polymer electrolyte containing 15 wt% LiTFSI featured an oxidative stability of up to 5.5 V vs. Li/Li + at 45 °C and a conductivity of 1.45 × 10 −8 S cm −1 at room temperature. This study describes the first example of the polymerization of water as one of two monomers. The obtained polymer allows for a solvent-free preparation of polymer electrolyte membranes exhibiting a high oxidative stability.
Bibliography:https://doi.org/10.1039/d2sc02124b
Electronic supplementary information (ESI) available. See
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ISSN:2041-6520
2041-6539
DOI:10.1039/d2sc02124b