Evidence map›Paper›PMID 39172896›Full record

ArticleChemSusChem2024

Azolium-Porphyrin Electrosynthesis.

Fatima Akhssas, Rongning Lin, Michal Trojan, Ludivine Poyac, Nesrine Amiri, Thibault Ertel, Sophie Fournier, Emmanuel Lerayer, Hélène Cattey, Sébastien Clément and 2 more

Abstract read
In one paragraph

Article in ChemSusChem, 2024. 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

12 authors.

Fatima AkhssasInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.
Rongning LinInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.
Michal TrojanInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.ORCID https://orcid.org/0000-0002-3894-1354
Ludivine PoyacICGM, Univ. Montpellier, CNRS, ENSCM, 34293, Montpellier, France.
Nesrine AmiriInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.ORCID https://orcid.org/0000-0003-2102-2738
Thibault ErtelInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.
Sophie FournierInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.
Emmanuel LerayerInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.
Hélène CatteyInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.
Sébastien ClémentICGM, Univ. Montpellier, CNRS, ENSCM, 34293, Montpellier, France.ORCID https://orcid.org/0000-0002-8473-8197
Sébastien RicheterICGM, Univ. Montpellier, CNRS, ENSCM, 34293, Montpellier, France.ORCID https://orcid.org/0000-0001-5284-0931
Charles H DevillersInstitut de Chimie Moléculaire de l'Université de Bourgogne UMR6302, CNRS, Univ. Bourgogne, 9 avenue Alain Savary, 21000, Dijon, France.ORCID https://orcid.org/0000-0001-9078-7035

Funding

Agence Nationale de la Recherche 15-CE29-0018-01Agence Nationale de la Recherche 15-IDEX-03Agence Nationale de la Recherche 17-EURE-0002Agence Nationale de la Recherche 19-CE07-0009-01Agence Nationale de la Recherche 19-CE7-0009-02Agence Nationale de la Recherche 23-CE07-0020-01Agence Nationale de la Recherche 23-CE07-0020-02
6 · The paper itself

Abstract

Electrochemical oxidation of Zn(II) 2,7,12,17-tetra-tert-butylporphyrin in the presence of a series of azole derivatives (1-methylimidazole, 1-vinyl-1H-imidazole, 2-(1H-imidazol-1-yl)pyridine, 1-methylbenzimidazole, 1-methyl-1H-1,2,4-triazole, and benzothiazole) affords the corresponding meso-substituted azolium-porphyrins in very mild conditions and good yields. It was found that these nucleophiles were strongly ligated to the zinc(II) azolium-porphyrin complexes. Thus a demetalation/remetalation procedure was performed to recover the non-azole-coordinated zinc(II) complexes. X-ray crystallographic structures of three azolium-porphyrins were solved. Cyclic voltammetry analyses provided insight into the electron-withdrawing effect of the azolium substituents.

Indexed as

Anodic nucleophilic substitutionAzole nucleophilesAzoliumElectrochemistryElectrosynthesisPorphyrinoids

Identifiers

PMID39172896
PMCPMC11660742

What OpenQuestion holds

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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.