Evidence map›Paper›PMID 40202364›Full record

ReviewChemistry, an Asian journal2025

Planar, Twisted, or Curved Extended Tetrathiafulvalenes with Polycyclic Aromatic Hydrocarbon Cores Featuring Five-Membered Rings.

Viktor Bliksted Roug Pedersen, Mogens Brøndsted Nielsen

Abstract readReview
In one paragraph

Review in Chemistry, an Asian journal, 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

2 authors.

Viktor Bliksted Roug PedersenDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, Copenhagen Ø, DK-2100, Denmark.
Mogens Brøndsted NielsenDepartment of Chemistry, University of Copenhagen, Universitetsparken 5, Copenhagen Ø, DK-2100, Denmark.

Funding

Novo Nordisk Foundation NNF20OC0061574
6 · The paper itself

Abstract

Tetrathiafulvalene (TTF) and polycyclic aromatic hydrocarbons (PAHs) represent two distinct classes of redox-active chromophores. By merging these two classes in so-called extended tetrathiafulvalenes, new physico-chemical characteristics emerge. Here in this study, we summarize the properties of such PAH-extended TTFs for which the PAH core incorporates five-membered carbo-cyclic rings together with six-, seven-, and/or eight-membered rings. A key structural motif of these molecules is the planar 2-(1H-inden-1-ylidene)-1,3-dithiole unit. Fusing two such units directly together or via various one- or two-dimensional PAH scaffolds has during the past decade provided a large selection of planar, twisted, or curved extended TTFs. Strong associations of radical cations are in some cases obtained, corresponding to redox-controlled self-assembly in solution, and these associations have allowed for the ready generation of semi-conducting salts by electrocrystallization. Some molecules exhibit remarkable multiredox behavior and can reversibly reach high cationic states, and, in some cases, also anionic states. Several structural examples also reveal how closed-shell versus open-shell characters of the dication states can be controlled by the nature of the PAH core, particularly by the number of Clar sextets within the core.

Indexed as

AromaticityConjugationFused‐ring systemsPolycyclesSulfur heterocycles

Identifiers

PMID40202364
PMCPMC12067868

What OpenQuestion holds

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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.