Evidence map›Paper›PMID 35774179›Full record

ArticleChemical science2022

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

Karin Ratzenböck, Mir Mehraj Ud Din, Susanne M Fischer, Ema Žagar, David Pahovnik, A Daniel Boese, Daniel Rettenwander, Christian Slugovc

Abstract read
In one paragraph

Article in Chemical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Karin RatzenböckChristian Doppler Laboratory for Organocatalysis in Polymerization Stremayrgasse 9 8010 Graz Austria slugovc@tugraz.at.ORCID https://orcid.org/0000-0002-5167-0739
Mir Mehraj Ud DinDepartment of Material Science and Engineering, NTNU Norwegian University of Science and Technology Sem Sælands vei 12 7034 Trondheim Norway.ORCID https://orcid.org/0000-0001-6501-3476
Susanne M FischerChristian Doppler Laboratory for Organocatalysis in Polymerization Stremayrgasse 9 8010 Graz Austria slugovc@tugraz.at.ORCID https://orcid.org/0000-0002-8187-1902
Ema ŽagarNational Institute of Chemistry, Department of Polymer Chemistry and Technology Hajdrihova 19 1000 Ljubljana Slovenia.ORCID https://orcid.org/0000-0002-2694-4312
David PahovnikNational Institute of Chemistry, Department of Polymer Chemistry and Technology Hajdrihova 19 1000 Ljubljana Slovenia.ORCID https://orcid.org/0000-0001-8024-8871
A Daniel BoesePhysical and Theoretical Chemistry, Institute of Chemistry, University of Graz Heinrichstrasse 28/IV 8010 Graz Austria.ORCID https://orcid.org/0000-0001-7388-778X
Daniel RettenwanderDepartment of Material Science and Engineering, NTNU Norwegian University of Science and Technology Sem Sælands vei 12 7034 Trondheim Norway.ORCID https://orcid.org/0000-0002-2074-941X
Christian SlugovcChristian Doppler Laboratory for Organocatalysis in Polymerization Stremayrgasse 9 8010 Graz Austria slugovc@tugraz.at.ORCID https://orcid.org/0000-0003-1873-5200

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

Identifiers

PMID35774179
PMCPMC9200112

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.