Evidence map›Paper›PMID 37592977›Full record

ArticleChemical science2023

Curved graphene nanoribbons derived from tetrahydropyrene-based polyphenylenes

Sebastian Obermann, Wenhao Zheng, Jason Melidonie, Steffen Böckmann, Silvio Osella, Nicolás Arisnabarreta, L Andrés Guerrero-León, Felix Hennersdorf, David Beljonne, Jan J Weigand and 6 more

Abstract read
In one paragraph

Article in Chemical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. A Negatively Curved Pyrene-Fused Azaacene.Angewandte Chemie (International ed. in English) · 2026
    Article
  2. Article
  3. Article
  4. Laterally π-Extended Polyhelicenes.Journal of the American Chemical Society · 2025
    Article
  5. 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

16 authors.

Sebastian ObermannCenter for Advancing Electronics Dresden (cfaed), Faculty of Chemistry and Food Chemistry, Technische Universität Dresden D-01069 Dresden Germany xinliang.feng@tu-dresden.de.ORCID https://orcid.org/0000-0002-3035-5772
Wenhao ZhengMax-Planck-Institute for Polymer Research D-55128 Mainz Germany.
Jason MelidonieCenter for Advancing Electronics Dresden (cfaed), Faculty of Chemistry and Food Chemistry, Technische Universität Dresden D-01069 Dresden Germany xinliang.feng@tu-dresden.de.
Steffen BöckmannInstitute of Physical Chemistry, Westfählische Wilhelms-Universität (WWU) Münster D-48149 Münster Germany.ORCID https://orcid.org/0000-0003-4383-7719
Silvio OsellaChemical and Biological Systems Simulation Lab, Centre of New Technologies University of Warsaw Banacha 2C Warsaw 02-097 Poland.ORCID https://orcid.org/0000-0001-8541-1914
Nicolás ArisnabarretaDepartment of Chemistry, Division of Molecular Imaging and Photonics, KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium.ORCID https://orcid.org/0000-0002-9546-1250
L Andrés Guerrero-LeónCenter for Advancing Electronics Dresden (cfaed), Faculty of Chemistry and Food Chemistry, Technische Universität Dresden D-01069 Dresden Germany xinliang.feng@tu-dresden.de.
Felix HennersdorfChair of Inorganic Molecular Chemistry, Technische Universität Dresden Dresden Germany.
David BeljonneLaboratory for Chemistry of Novel Materials, Materials Research Institute, University of Mons Mons 7000 Belgium.ORCID https://orcid.org/0000-0001-5082-9990
Jan J WeigandChair of Inorganic Molecular Chemistry, Technische Universität Dresden Dresden Germany.ORCID https://orcid.org/0000-0001-7323-7816
Mischa BonnMax-Planck-Institute for Polymer Research D-55128 Mainz Germany.ORCID https://orcid.org/0000-0001-6851-8453
Steven De FeyterDepartment of Chemistry, Division of Molecular Imaging and Photonics, KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium.ORCID https://orcid.org/0000-0002-0909-9292
Michael Ryan HansenInstitute of Physical Chemistry, Westfählische Wilhelms-Universität (WWU) Münster D-48149 Münster Germany.ORCID https://orcid.org/0000-0001-7114-8051
Hai I WangMax-Planck-Institute for Polymer Research D-55128 Mainz Germany.ORCID https://orcid.org/0000-0003-0940-3984
Ji MaCenter for Advancing Electronics Dresden (cfaed), Faculty of Chemistry and Food Chemistry, Technische Universität Dresden D-01069 Dresden Germany xinliang.feng@tu-dresden.de.ORCID https://orcid.org/0000-0003-4418-2339
Xinliang FengCenter for Advancing Electronics Dresden (cfaed), Faculty of Chemistry and Food Chemistry, Technische Universität Dresden D-01069 Dresden Germany xinliang.feng@tu-dresden.de.ORCID https://orcid.org/0000-0003-3885-2703

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise synthesis of graphene nanoribbons (GNRs) is of great interest to chemists and materials scientists because of their unique opto-electronic properties and potential applications in carbon-based nanoelectronics and spintronics. In addition to the tunable edge structure and width, introducing curvature in GNRs is a powerful structural feature for their chemi-physical property modification. Here, we report an efficient solution synthesis of the first pyrene-based GNR (PyGNR) with curved geometry

Identifiers

PMID37592977
PMCPMC10430550

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.