Evidence map›Paper›PMID 41145469›Full record

ArticleNature communications2025

The successful impossible radical ring-opening copolymerization of thionolactones and methacrylates via an auxiliary third comonomer.

Bastien Luzel, Ignatii Efimov, Mariya Edeleva, Sophia Kouider, Noémie Gil, Damien Montarnal, Catherine Lefay, Didier Gigmes, Paul H M Van Steenberge, Dagmar R D'hooge and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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

11 authors.

Bastien LuzelAix-Marseille University, CNRS, Institut de Chimie Radicalaire, UMR 7273, F-13397, Marseille, France.
Ignatii EfimovLaboratory for Chemical Technology (LCT), Ghent University, Technologiepark 125, 9052, Ghent, Belgium.ORCID http://orcid.org/0000-0002-1748-7172
Mariya EdelevaLaboratory for Chemical Technology (LCT), Ghent University, Technologiepark 125, 9052, Ghent, Belgium.
Sophia KouiderAix-Marseille University, CNRS, Institut de Chimie Radicalaire, UMR 7273, F-13397, Marseille, France.
Noémie GilAix-Marseille University, CNRS, Institut de Chimie Radicalaire, UMR 7273, F-13397, Marseille, France.
Damien MontarnalUniversity of Lyon, CPE Lyon, CNRS, Catalyse, Polymerization, Processes and Materials, UMR 5128, F-69003, Lyon, France.ORCID http://orcid.org/0000-0003-3246-3467
Catherine LefayAix-Marseille University, CNRS, Institut de Chimie Radicalaire, UMR 7273, F-13397, Marseille, France.
Didier GigmesAix-Marseille University, CNRS, Institut de Chimie Radicalaire, UMR 7273, F-13397, Marseille, France.
Paul H M Van SteenbergeAix-Marseille University, CNRS, Institut de Chimie Radicalaire, UMR 7273, F-13397, Marseille, France.ORCID http://orcid.org/0000-0001-6244-1299
Dagmar R D'hoogeLaboratory for Chemical Technology (LCT), Ghent University, Technologiepark 125, 9052, Ghent, Belgium. dagmar.dhooge@ugent.be.ORCID http://orcid.org/0000-0001-9663-9893
Yohann GuillaneufAix-Marseille University, CNRS, Institut de Chimie Radicalaire, UMR 7273, F-13397, Marseille, France. yohann.guillaneuf@univ-amu.fr.ORCID http://orcid.org/0000-0002-5390-1553

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymethacrylate derivatives are widely used in various industrial applications. The incorporation of degradable thioester bonds in polymethacrylates to achieve degradability/recyclability upon disposal is a challenge. Unfortunately, the most efficient thionolactone to insert cleavable thioester linkages does not copolymerize with methacrylates. We show that a small amount of the thionolactone can be inserted into polymethacrylates by the use of methyl acrylate or N-phenyl maleimide as an auxiliary third comonomer. We confirmed the selective degradation of the copolymer via aminolysis. The intriguing incorporation of the thionolactone via the formation of triads is demonstrated using Monte Carlo simulations and such method is also used to optimize the synthesis conditions. Copolymers of 60,000 g.mol

Identifiers

PMID41145469
PMCPMC12559751

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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.