Evidence map›Paper›PMID 40551005›Full record

ArticleMacromolecular rapid communications2025

Furan-Protected 4-Maleimidomethyl Styrene for Reversible Crosslinked Polymers.

Alfred Andreas Hamm, Gregor Schnakenburg, Sigurd Höger

Abstract read
In one paragraph

Article in Macromolecular rapid communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Alfred Andreas HammKekulé-Institut für Organische Chemie und Biochemie, University of Bonn, Bonn, Germany.
Gregor SchnakenburgInstitut für Anorganische Chemie, University of Bonn, Bonn, Germany.
Sigurd HögerKekulé-Institut für Organische Chemie und Biochemie, University of Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0001-9987-0185

Funding

TRA Matter
6 · The paper itself

Abstract

Due to the growing interest in reversibly cross-linkable polymers, the synthesis of maleimide-containing polymers for Diels-Alder crosslinking is very attractive. Here we present two new synthetic approaches to such polymers, starting from an N-alkylation of furane-protected maleimide, either at the polymeric level with poly(styrene-stat-4-chloromethylstyrene) or at the level of monomeric structures with 4-chloromethylstyrene. Both strategies allow freely adjustable maleimide contents and copolymerization with various comonomers. The monomer used for the second route has not yet been described in this form and is therefore examined in more detail, particularly with regard to its copolymerization behavior. We also present the reversibility of the cross-linking reaction and the possibility of integrating further functional groups into the polymer.

Indexed as

Cross-Linking ReagentsFuransMaleimidesPolymersPolystyrenesMolecular StructurePolymerizationCross-Linking ReagentsfuranFuransmaleimideMaleimidesPolymersPolystyrenesDiels‐Alder reactionmaleimidomethyl styreneself‐healingthermoreversible crosslinking

Identifiers

PMID40551005
PMCPMC12687677

What OpenQuestion holds

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Registered trials

None linked

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.