Evidence map›Paper›PMID 34014601›Full record

ArticleAngewandte Chemie (International ed. in English)2021

A Family of Superhelicenes: Easily Tunable, Chiral Nanographenes by Merging Helicity with Planar π Systems.

David Reger, Philipp Haines, Konstantin Y Amsharov, Julia A Schmidt, Tobias Ullrich, Simon Bönisch, Frank Hampel, Andreas Görling, Jenny Nelson, Kim E Jelfs and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.7field-weighted citation impact, top 2% of its field
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

23 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
  2. Article
  3. A Chiral Saddle-Shaped Nanographene With Two Heptagon-Embedded [4]Helicenes.Angewandte Chemie (International ed. in English) · 2026
    Article
  4. Article
  5. Article
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  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Construction of hexabenzocoronene-based chiral nanographenes.Beilstein journal of organic chemistry · 2023
    Review
  16. Article
  17. Chemo- and Regioselective Multiple C(spAngewandte Chemie (International ed. in English) · 2022
    Article
  18. Article
  19. Article
  20. 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

12 authors at 3 institutions in 2 countries.

David RegerDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Nikolaus-Fiebiger-Straße 10, 91058, Erlangen, Germany.ORCID http://orcid.org/0000-0002-9407-3408
Philipp HainesDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Egerlandstraße 3, 91058, Erlangen, Germany.
Konstantin Y AmsharovInstitute for Organic Chemistry, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 2, 06120, Halle, Germany.ORCID http://orcid.org/0000-0002-2854-8081
Julia A SchmidtDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, White City Campus, Wood Lane, London, W12 0BZ, UK.ORCID http://orcid.org/0000-0002-5934-3257
Tobias UllrichDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Egerlandstraße 3, 91058, Erlangen, Germany.
Simon BönischDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Egerlandstraße 3, 91058, Erlangen, Germany.ORCID http://orcid.org/0000-0002-0269-6828
Frank HampelDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Nikolaus-Fiebiger-Straße 10, 91058, Erlangen, Germany.ORCID http://orcid.org/0000-0001-9768-782X
Andreas GörlingDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Egerlandstraße 3, 91058, Erlangen, Germany.ORCID http://orcid.org/0000-0002-1831-3318
Jenny NelsonDepartment of Physics, Imperial College London, South Kensington Campus, London, SW7 2AZ, UK.ORCID http://orcid.org/0000-0003-1048-1330
Kim E JelfsDepartment of Chemistry, Molecular Sciences Research Hub, Imperial College London, White City Campus, Wood Lane, London, W12 0BZ, UK.ORCID http://orcid.org/0000-0001-7683-7630
Dirk M GuldiDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Egerlandstraße 3, 91058, Erlangen, Germany.ORCID http://orcid.org/0000-0002-3960-1765
Norbert JuxDepartment of Chemistry and Pharmacy & Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-University Erlangen-Nuremberg, Nikolaus-Fiebiger-Straße 10, 91058, Erlangen, Germany.ORCID http://orcid.org/0000-0002-5673-8181
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEImperial College London · GBMartin Luther University Halle-Wittenberg · DE

Funding

Deutsche Forschungsgemeinschaft 182849149Graduate School of Molecular Science, Friedrich-Alexander-Universität Erlangen-Nürnberg
6 · The paper itself

Abstract

We designed a straightforward synthetic route towards a full-fledged family of π-extended helicenes: superhelicenes. They have two hexa-peri-hexabenzocoronenes (HBCs) in common that are connected via a central five-membered ring. By means of structurally altering this 5-membered ring, we realized a versatile library of molecular building blocks. Not only the superhelicene structure, but also their features are tuned with ease. In-depth physico-chemical characterizations served as a proof of concept thereof. The superhelicene enantiomers were separated, their circular dichroism was measured in preliminary studies and concluded with an enantiomeric assignment. Our work was rounded-off by crystal structure analyses. Mixed stacks of M- and P-isomers led to twisted molecular wires. Using such stacks, charge-carrier mobilities were calculated, giving reason to expect outstanding hole transporting properties.

Indexed as

circular dichroismhelicenesluminescencenanographenepolycyclic aromatic hydrocarbons

Identifiers

PMID34014601
PMCPMC8456895
OpenAlexW3160727641

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.