Evidence map›Paper›PMID 35064118›Full record

ArticleNature communications2022

Controlling the helicity of π-conjugated oligomers by tuning the aromatic backbone twist.

Anjan Bedi, Amit Manor Armon, Yael Diskin-Posner, Benny Bogosalvsky, Ori Gidron

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Exciton trapping with a twist.Chemical science · 2026
    Article
  3. Article
  4. Article
  5. Controlling the Helicity and Handedness of Polyaromatics with Isobenzofuranophane.Angewandte Chemie (International ed. in English) · 2025
    Article
  6. Article
  7. Article
  8. Synthesis of optically active folded cyclic dimers and trimers.Beilstein journal of organic chemistry · 2025
    Article
  9. Article
  10. Article
  11. Optical Activity and Spin Polarization: The Surface Effect.Journal of the American Chemical Society · 2023
    Article
  12. Article
  13. Light-Responsive Oligothiophenes Incorporating Photochromic Torsional Switches.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022
    Article
  14. Article
  15. 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

5 authors.

Anjan BediInstitute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Edmond J. Safra Campus, 9190401, Jerusalem, Israel.ORCID http://orcid.org/0000-0001-6418-4409
Amit Manor ArmonInstitute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Edmond J. Safra Campus, 9190401, Jerusalem, Israel.
Yael Diskin-PosnerChemical Research Support Unit, Weizmann Institute of Science, 7610001, Rehovot, Israel.ORCID http://orcid.org/0000-0002-9008-8477
Benny BogosalvskyInstitute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Edmond J. Safra Campus, 9190401, Jerusalem, Israel.ORCID http://orcid.org/0000-0001-9555-170X
Ori GidronInstitute of Chemistry and the Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Edmond J. Safra Campus, 9190401, Jerusalem, Israel. ori.gidron@mail.huji.ac.il.ORCID http://orcid.org/0000-0002-7037-0563

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 850836
6 · The paper itself

Abstract

The properties of π-conjugated oligomers and polymers are commonly controlled by side group engineering, main chain engineering, or conformational engineering. The last approach is typically limited to controlling the dihedral angle around the interring single bonds to prevent loss of π-conjugation. Here we propose a different approach to conformational engineering that involves controlling the twist of the aromatic units comprising the backbone by using a tether of varying lengths. We demonstrate this approach by synthesizing an inherently twisted building unit comprised of helically locked tethered acenes, bearing acetylene end-groups to enable backbone extension, which was applied in a series of nine helical oligomers with varying backbone length and twist. We find that the optical and electronic properties of π-conjugated systems may be determined by the additive, antagonistic, or independent effects of backbone length and twist angle. The twisted oligomers display chiral amplification, arising from the formation of secondary helical structures.

Identifiers

PMID35064118
PMCPMC8782941

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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.