Evidence map›Paper›PMID 39286924›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Control of Dynamic Chirality in Donor-Acceptor Fluorophores.

Max Coehlo, Lucas Frédéric, Laurélie Poulard, Nawal Ferdi, Lilian Estaque, Alaric Desmarchelier, Gilles Clavier, Jean-Pierre Dognon, Ludovic Favereau, Michel Giorgi and 2 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  5. Article
  6. Review
  7. Control of Dynamic Chirality in Donor-Acceptor Fluorophores.Angewandte Chemie (International ed. in English) · 2025
    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

12 authors.

Max CoehloUniversité Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, F-91191, France.
Lucas FrédéricUniversité Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, F-91191, France.
Laurélie PoulardUniversité Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, F-91191, France.
Nawal FerdiAix Marseille Univ, CNRS, Centrale Med, FSCM, Marseille, France.
Lilian EstaqueUniversité Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, F-91191, France.
Alaric DesmarchelierUniversité Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, F-91191, France.
Gilles ClavierUniversité Paris-Saclay, ENS Paris-Saclay, CNRS, PPSM, Gif-sur-Yvette, F-91190, France.
Jean-Pierre DognonUniversité Paris-Saclay, CEA, CNRS, NIMBE, Gif-sur-Yvette, 91191, France.
Ludovic FavereauUniversité de Rennes, CNRS ISCR-UMR 6226, Rennes, 35042, France.
Michel GiorgiAix Marseille Univ, CNRS, Centrale Med, FSCM, Marseille, France.
Jean-Valère NaubronAix Marseille Univ, CNRS, Centrale Med, FSCM, Marseille, France.
Gregory PietersUniversité Paris-Saclay, CEA, INRAE, Département Médicaments et Technologies pour la Santé (DMTS), SCBM, Gif-sur-Yvette, F-91191, France.ORCID https://orcid.org/0000-0002-3924-8287

Funding

Agence Nationale de la Recherche ANR-19-CE07-0040Ministère de l'Education nationale, de l'Enseignement supérieur et de la Recherche
6 · The paper itself

Abstract

Recently, the control of dynamic chirality has emerged as a powerful strategy to design chiral functional materials. In this context, we describe herein a molecular design in which a tethered configurationally stable binaphthyl chiral unit efficiently controls the dynamic chirality of donor-acceptor fluorophores, involving diverse indolocarbazoles as electron donors and terephthalonitrile as an electron acceptor. The high conformational discrimination in such a molecular system suggested by density functional theory calculations is experimentally probed using electronic and vibrational circular dichroism and confirmed by the crystallization of these chiral molecules in gel and their single crystal X-ray diffraction analysis. This work also highlights the positive effect of the configurationally stable chiral unit on the magnitude of the dissymmetry factors of the active dynamically chiral fluorophores, both in ground and excited states, through chiral perturbation.

Indexed as

Chiral materialsCircularly polarized luminescenceDissymmetry factorElectronic circular dichroismVibrational circular dichroism

Identifiers

PMID39286924
PMCPMC11720384

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.