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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200112/ https://www.ncbi.nlm.nih.gov/pubmed/35774179 http://dx.doi.org/10.1039/d2sc02124b |
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author | Ratzenböck, Karin Ud Din, Mir Mehraj Fischer, Susanne M. Žagar, Ema Pahovnik, David Boese, A. Daniel Rettenwander, Daniel Slugovc, Christian |
author_facet | Ratzenböck, Karin Ud Din, Mir Mehraj Fischer, Susanne M. Žagar, Ema Pahovnik, David Boese, A. Daniel Rettenwander, Daniel Slugovc, Christian |
author_sort | Ratzenböck, Karin |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9200112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-92001122022-06-29 Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water Ratzenböck, Karin Ud Din, Mir Mehraj Fischer, Susanne M. Žagar, Ema Pahovnik, David Boese, A. Daniel Rettenwander, Daniel Slugovc, Christian Chem Sci Chemistry 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. The Royal Society of Chemistry 2022-05-23 /pmc/articles/PMC9200112/ /pubmed/35774179 http://dx.doi.org/10.1039/d2sc02124b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Ratzenböck, Karin Ud Din, Mir Mehraj Fischer, Susanne M. Žagar, Ema Pahovnik, David Boese, A. Daniel Rettenwander, Daniel Slugovc, Christian Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water |
title | Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water |
title_full | Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water |
title_fullStr | Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water |
title_full_unstemmed | Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water |
title_short | Water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water |
title_sort | water as a monomer: synthesis of an aliphatic polyethersulfone from divinyl sulfone and water |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200112/ https://www.ncbi.nlm.nih.gov/pubmed/35774179 http://dx.doi.org/10.1039/d2sc02124b |
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