Evidence map›Paper›PMID 41168649›Full record

ArticleChemistry, an Asian journal2025

Synthesis, Photophysical Properties, and Practical Hg(II)-Sensing Applications of a Rigidified Phenolo-Merocyanine Dye.

Kévin Renault, Zuzana Pohancenikova, Maël Croizier, Vincent Gaumerd, Manhattan Lebrun, Michel Chalot, Anthony Romieu

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 2025. 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

7 authors.

Kévin RenaultInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR 6302, Univ. Bourgogne Europe, CNRS, 9, Avenue Alain Savary, Dijon, F-21000, France.ORCID https://orcid.org/0000-0003-4427-8146
Zuzana PohancenikovaInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR 6302, Univ. Bourgogne Europe, CNRS, 9, Avenue Alain Savary, Dijon, F-21000, France.
Maël CroizierInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR 6302, Univ. Bourgogne Europe, CNRS, 9, Avenue Alain Savary, Dijon, F-21000, France.
Vincent GaumerdInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR 6302, Univ. Bourgogne Europe, CNRS, 9, Avenue Alain Savary, Dijon, F-21000, France.ORCID https://orcid.org/0009-0000-0126-7864
Manhattan LebrunUniversité Marie et Louis Pasteur, CNRS, Chrono-environnement, UMR 6249, Montbéliard, F-25200, France.ORCID https://orcid.org/0000-0002-8528-3040
Michel ChalotUniversité Marie et Louis Pasteur, CNRS, Chrono-environnement, UMR 6249, Montbéliard, F-25200, France.ORCID https://orcid.org/0000-0001-8614-0917
Anthony RomieuInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR 6302, Univ. Bourgogne Europe, CNRS, 9, Avenue Alain Savary, Dijon, F-21000, France.ORCID https://orcid.org/0000-0002-2300-4499

Funding

Agence de l'Environnement et de la Maîtrise de l'EnergieAgence de l'Innovation de Défense 2022006Agence Nationale de la Recherche ANR-18-CE07-0045Agence Nationale de la Recherche ANR-20-CE22-0010CNRS, MITI 279647Secrétariat Général pour l'Investissement : "Territory of Innovation" of the Investment for the Future Program (PIA3).
6 · The paper itself

Abstract

Among the strategies available to improve photophysical properties of organic fluorophores intended for imaging and sensing, structural modifications allowing for scaffold rigidification are particularly effective for enhancing yellow emission and photostability. In order to develop novel high-performance phenolic fluorophores, we have explored the synthesis of a conformationally restrained analog of flexible Brooker's merocyanine. We had the idea of applying a rigidification approach previously devised for cyanine dyes. Thus, the implementation of an acid-catalyzed domino double cyclization process allowed the synthesis of fluorescent phenol KR306. A comprehensive photophysical study has highlighted its outstanding optical properties in neutral aq. buffered conditions (a brightness of 71,500 M

Indexed as

conformational restrictionhydroxyl group protection‐deprotectionmercuric cationmerocyanine dyereaction‐based fluorescent probethiophosphinate ester

Identifiers

PMID41168649
PMCPMC12696781

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.