Evidence map›Paper›PMID 42686834›Full record

ArticleNature chemistry2026

Lower-temperature bulk depolymerization of commercial polymethacrylates.

Richard Whitfield, Victoria Lohmann, Mikhail Agrachev, Hongsik Kim, Hyun Suk Wang, Nethmi De Alwis Watuthanthrige, Nghia P Truong, Tae-Lim Choi, Gunnar Jeschke, Athina Anastasaki

Abstract read
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In one paragraph

Article in Nature chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Richard WhitfieldLaboratory of Sustainable Polymers, Department of Materials, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0003-4787-2060
Victoria LohmannLaboratory of Sustainable Polymers, Department of Materials, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-5516-7439
Mikhail AgrachevInstitute for Molecular Physical Science, Department of Chemistry and Applied Biosciences, ETH Zurich, Zurich, Switzerland.
Hongsik KimLaboratory of Polymer Chemistry, Department of Materials, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-9469-6699
Hyun Suk WangLaboratory of Sustainable Polymers, Department of Materials, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-2515-3906
Nethmi De Alwis WatuthanthrigeLaboratory of Sustainable Polymers, Department of Materials, ETH Zurich, Zurich, Switzerland.
Nghia P TruongLaboratory of Sustainable Polymers, Department of Materials, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-9900-2644
Tae-Lim ChoiLaboratory of Polymer Chemistry, Department of Materials, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-9521-6450
Gunnar JeschkeInstitute for Molecular Physical Science, Department of Chemistry and Applied Biosciences, ETH Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-6853-8585
Athina AnastasakiLaboratory of Sustainable Polymers, Department of Materials, ETH Zurich, Zurich, Switzerland. athina.anastasaki@mat.ethz.ch.ORCID http://orcid.org/0000-0002-6615-1026

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 949219
6 · The paper itself

Abstract

Chemical recycling back to monomer represents an attractive methodology to tackle plastic waste. However, current reports focus on either thermally unstable 'designer' polymers or highly diluted solution depolymerizations. Here we report a simple, yet efficient, bulk main-chain scission pathway, whereby the presence of N-hydroxyphthalimides triggers a hydrogen-atom-transfer reaction on the polymer backbone, followed by the rapid and near-quantitative depolymerization of polymethacrylates. Notably, this strategy can be directly applied to crude commercial polymers, does not rely on preinstalled end-groups or sacrificial co-monomers, operates at relatively low temperatures in the absence of light irradiation and precludes the use of a solvent, therefore enabling direct isolation of pristine monomers in high yields (∼90%). The methodology is compatible with polymethacrylates synthesized by either anionic, free radical or controlled radical polymerization and can also be applied to ultrahigh-molecular-weight materials (>10

Identifiers

PMID42686834

What OpenQuestion holds

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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.