Evidence map›Paper›PMID 38355475›Full record

ArticleJournal of the American Chemical Society2024

A Chirally Locked Bis-perylene Diimide Macrocycle: Consequences for Chiral Self-Assembly and Circularly Polarized Luminescence.

Samuel E Penty, Georgia R F Orton, Dominic J Black, Robert Pal, Martijn A Zwijnenburg, Timothy A Barendt

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. A Bis-Perylene Diimide Macrocycle Chiroptical Switch.Angewandte Chemie (International ed. in English) · 2025
    Article
  13. Twisted Nanographenes with Robust Conformational Stability.Nanomaterials (Basel, Switzerland) · 2024
    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

6 authors.

Samuel E PentySchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K.ORCID 0000-0003-4554-0855
Georgia R F OrtonSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K.ORCID 0000-0002-7566-0092
Dominic J BlackDepartment of Chemistry, University of Durham, South Road, Durham DH1 3LE, U.K.
Robert PalDepartment of Chemistry, University of Durham, South Road, Durham DH1 3LE, U.K.ORCID 0000-0002-0641-4218
Martijn A ZwijnenburgDepartment of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, U.K.ORCID 0000-0001-5291-2130
Timothy A BarendtSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K.ORCID 0000-0002-9806-4381

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrocycles containing chiral organic dyes are highly valuable for the development of supramolecular circularly polarized luminescent (CPL) materials, where a preorganized chiral framework is conducive to directing π-π self-assembly and delivering a strong and persistent CPL signal. Here, perylene diimides (PDIs) are an excellent choice for the organic dye component because, alongside their tunable photophysical and self-assembly properties, functionalization of the PDI's core yields a twisted, chiral π-system, capable of CPL. However, configurationally stable PDI-based macrocycles are rare, and those that are also capable of π-π self-assembly beyond dimers are unprecedented, both of which are advantageous for robust self-assembled chiroptical materials. In this work, we report the first bay-connected bis-PDI macrocycle that is configurationally stable (Δ

Identifiers

PMID38355475
PMCPMC10910538

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Registered trials

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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.