Evidence map›Paper›PMID 40203208›Full record

ArticleChemphyschem : a European journal of chemical physics and physical chemistry2025

Bromo-Heptahelicene-Bis-Thiadiazole: Photophysics, Chiroptics, and Excited-State Dynamics.

Debsouri Kundu, Rituparno Chowdhury, Natalia Del Rio, Marie Cordier, Nicolas Vanthuyne, Richard H Friend, Monika Srebro-Hooper, Jeanne Crassous

Abstract read
In one paragraph

Article in Chemphyschem : a European journal of chemical physics and physical chemistry, 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. Review
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

8 authors.

Debsouri KunduInstitut des Sciences Chimiques de Rennes, Univ Rennes, UMR CNRS 6226, Campus de Beaulieu, 35042, Rennes Cedex, France.
Rituparno ChowdhuryThe Cavendish Laboratory, University of Cambridge, J. J. Thomson Avenue, Cambridge, CB3 0HE, UK.ORCID https://orcid.org/0000-0003-3063-4576
Natalia Del RioInstitut des Sciences Chimiques de Rennes, Univ Rennes, UMR CNRS 6226, Campus de Beaulieu, 35042, Rennes Cedex, France.ORCID https://orcid.org/0000-0001-9179-881X
Marie CordierInstitut des Sciences Chimiques de Rennes, Univ Rennes, UMR CNRS 6226, Campus de Beaulieu, 35042, Rennes Cedex, France.
Nicolas VanthuyneAix Marseille Univ, CNRS, Centrale Med, FSCM, 13397, Marseille, France.ORCID https://orcid.org/0000-0003-2598-7940
Richard H FriendThe Cavendish Laboratory, University of Cambridge, J. J. Thomson Avenue, Cambridge, CB3 0HE, UK.ORCID https://orcid.org/0000-0001-6565-6308
Monika Srebro-HooperFaculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387, Krakow, Poland.ORCID https://orcid.org/0000-0003-4211-325X
Jeanne CrassousInstitut des Sciences Chimiques de Rennes, Univ Rennes, UMR CNRS 6226, Campus de Beaulieu, 35042, Rennes Cedex, France.ORCID https://orcid.org/0000-0002-4037-6067

Funding

Ecole Universitaire de Recherche de Chimie (EUR LUMOMAT); Rennes MétropoleEuropean Commission Research Executive Agency 859752 - HEL4CHIROLED - H2020-MSCA-ITN-2019Polish High-Performance Computing Infrastructure PLGrid PLG/2023/016362
6 · The paper itself

Abstract

The synthesis of a [7]helicene bromide derivative with two fused 2,1,3-thiadiazole heterocycles (TD[7]Br) and a comprehensive study of its photophysical and chiroptical characteristics are presented along with a comparison with 9-bromo-carbo[7]helicene ([7]Br) and 2,15-dibromo-carbo[6]helicene ([6]Br). The integration of a bromine heavy atom onto the helicene backbone facilitates efficient singlet-to-triplet conversion allowing to investigate the resulting fluorescence and phosphorescence properties. The steady-state chiroptical features of the systems are demonstrated through electronic circular dichroism and circularly polarized luminescence. Interestingly, a fluorescence quantum yield of 14% is obtained, a 17-fold increase compared to the corresponding bromo-heptacarbohelicene, and phosphorescence dissymmetry factors reach ±1.2 × 10

Indexed as

chiropticsheavy‐atom effectsheptahelicenesphotophysicstime‐dependent density functional theory calculations

Identifiers

PMID40203208
PMCPMC12321275

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.