Evidence map›Paper›PMID 38903211›Full record

ArticleChemical science2024

Copper-catalysed perarylation of cyclopentadiene: synthesis of hexaarylcyclopentadienes.

Yohan Gisbert, Pablo Simón Marqués, Caterina Baccini, Seifallah Abid, Nathalie Saffon-Merceron, Gwénaël Rapenne, Claire Kammerer

Abstract read
In one paragraph

Article in Chemical science, 2024. 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.

Yohan GisbertCEMES, Université de Toulouse, CNRS 29 Rue Marvig 31055 Toulouse France claire.kammerer@cemes.fr.ORCID https://orcid.org/0000-0002-6671-4538
Pablo Simón MarquésCEMES, Université de Toulouse, CNRS 29 Rue Marvig 31055 Toulouse France claire.kammerer@cemes.fr.ORCID https://orcid.org/0000-0001-7421-8473
Caterina BacciniCEMES, Université de Toulouse, CNRS 29 Rue Marvig 31055 Toulouse France claire.kammerer@cemes.fr.
Seifallah AbidCEMES, Université de Toulouse, CNRS 29 Rue Marvig 31055 Toulouse France claire.kammerer@cemes.fr.
Nathalie Saffon-MerceronUniversité de Toulouse, UPS, Institut de Chimie de Toulouse ICT UAR 2599, 118 Route de Narbonne 31062 Toulouse France.
Gwénaël RapenneCEMES, Université de Toulouse, CNRS 29 Rue Marvig 31055 Toulouse France claire.kammerer@cemes.fr.ORCID https://orcid.org/0000-0002-4993-4213
Claire KammererCEMES, Université de Toulouse, CNRS 29 Rue Marvig 31055 Toulouse France claire.kammerer@cemes.fr.ORCID https://orcid.org/0000-0002-5292-5975

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While hexaphenylsilacyclopentadiene (hexaphenylsilole) is viewed as an archetypal Aggregation-Induced Emission (AIE) luminogen, its isostructural hydrocarbon surrogate hexaphenylcyclopentadiene has strikingly never been investigated in this context, most probably due to a lack of synthetic availability. Herein, we report a straightforward synthesis of hexaphenylcyclopentadiene,

Identifiers

PMID38903211
PMCPMC11186316

What OpenQuestion holds

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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.