Evidence map›Paper›PMID 40121190›Full record

ArticleNature communications2025

Enantiopure synthesis of [5]helicene based molecular lemniscates and their use in chiroptical materials.

Leah E M White, Tiberiu-M Gianga, Fabienne Pradaux-Caggiano, Chiara Faverio, Andrea Taddeucci, Henry S Rzepa, Christian Jonhannesen, Lauren E Hatcher, Giuliano Siligardi, David R Carbery and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Leah E M WhiteDepartment of Chemistry, University of Bath, Bath, UK.
Tiberiu-M GiangaB23 Beamline, Diamond Light Source Ltd., Didcot, UK.ORCID http://orcid.org/0000-0002-6081-874X
Fabienne Pradaux-CaggianoDepartment of Chemistry, University of Bath, Bath, UK.
Chiara FaverioDepartment of Chemistry, University of Bath, Bath, UK.ORCID http://orcid.org/0000-0002-3260-3944
Andrea TaddeucciB23 Beamline, Diamond Light Source Ltd., Didcot, UK.ORCID http://orcid.org/0009-0003-4467-7283
Henry S RzepaDepartment of Chemistry, Imperial College London MSRH, London, UK.
Christian JonhannesenDepartment of Chemistry, University of Antwerp, Antwerp, Belgium.ORCID http://orcid.org/0000-0003-2613-9476
Lauren E HatcherSchool of Chemistry, Cardiff University, Cardiff, UK.
Giuliano SiligardiB23 Beamline, Diamond Light Source Ltd., Didcot, UK.ORCID http://orcid.org/0000-0002-4667-6423
David R CarberyDepartment of Chemistry, University of Bath, Bath, UK.
G Dan PantoșDepartment of Chemistry, University of Bath, Bath, UK. g.d.pantos@bath.ac.uk.ORCID http://orcid.org/0000-0003-2200-550X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to synthesise lemniscular molecules to allow for the study and application of their chiroptical properties is a notable technical challenge. Herein, we report the design and synthesis of enantiomers of a [5]helicenoid derived molecular lemniscate, in which two homochiral helicenes are linked via the formation of two azine motifs. We demonstrate that these molecules, and their helicenoid constituents, are also excellent chiral dopants that induce dissymmetry in the ground and excited states of the achiral emissive polymer F8BT, leading to high CPL activity. The ability to control the handedness of the helicenoid dopants via enantiopure synthesis affords control of the sign of CP emission. This manipulation of circularly polarised light is of great interest for optoelectronic technologies.

Identifiers

PMID40121190
PMCPMC11929746

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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.