Evidence map›Paper›PMID 27992878›Full record

ArticleNature2017

Aromatic and antiaromatic ring currents in a molecular nanoring.

Martin D Peeks, Timothy D W Claridge, Harry L Anderson

Abstract read
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In one paragraph

Article in Nature, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

53 citing papers in PubMed.

  1. Article
  2. Article
  3. An 18-Porphyrin Nanoring at the Size Limit for Global Aromaticity.Journal of the American Chemical Society · 2025
    Article
  4. Review
  5. Strong Ferromagnetic Coupling between Co and CoThe journal of physical chemistry. A · 2025
    Article
  6. Article
  7. Redox-Switchable Aromaticity in a Helically Extended Indeno[2,1-Journal of the American Chemical Society · 2024
    Article
  8. SynergisticChemical science · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Dynamic covalent synthesis.Chemical science · 2024
    Review
  15. Article
  16. Current-Density Calculations on Zn-PorphyrinThe journal of physical chemistry. A · 2023
    Article
  17. Tetra-tert-butyl-s-indacene is a Bond-Localized CAngewandte Chemie (International ed. in English) · 2023
    Article
  18. Article
  19. Aromaticity: Quo Vadis.Chemical science · 2023
    Review
  20. 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

3 authors.

Martin D PeeksUniversity of Oxford, Department of Chemistry, Chemistry Research Laboratory, Oxford OX1 3TA, UK.
Timothy D W ClaridgeUniversity of Oxford, Department of Chemistry, Chemistry Research Laboratory, Oxford OX1 3TA, UK.
Harry L AndersonUniversity of Oxford, Department of Chemistry, Chemistry Research Laboratory, Oxford OX1 3TA, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aromatic and antiaromatic molecules-which have delocalized circuits of [4n + 2] or [4n] electrons, respectively-exhibit ring currents around their perimeters. The direction of the ring current in an aromatic molecule is such as to generate a magnetic field that opposes the external field inside the ring (a 'diatropic' current), while the ring current in an antiaromatic molecule flows in the reverse direction ('paratropic'). Similar persistent currents occur in metal or semiconductor rings, when the phase coherence of the electronic wavefunction is preserved around the ring. Persistent currents in non-molecular rings switch direction as a function of the magnetic flux passing through the ring, so that they can be changed from diatropic ('aromatic') to paratropic ('antiaromatic') simply by changing the external magnetic field. As in molecular systems, the direction of the persistent current also depends on the number of electrons. The relationship between ring currents in molecular and non-molecular rings is poorly understood, partly because they are studied in different size regimes: the largest aromatic molecules have diameters of about one nanometre, whereas persistent currents are observed in microfabricated rings with diameters of 20-1,000 nanometres. Understanding the connection between aromaticity and quantum-coherence effects in mesoscopic rings provides a motivation for investigating ring currents in molecules of an intermediate size. Here we show, using nuclear magnetic resonance spectroscopy and density functional theory, that a six-porphyrin nanoring template complex, with a diameter of 2.4 nanometres, is antiaromatic in its 4+ oxidation state (80 π electrons) and aromatic in its 6+ oxidation state (78 π electrons). The antiaromatic state has a huge paramagnetic susceptibility, despite having no unpaired electrons. This work demonstrates that a global ring current can be promoted in a macrocycle by adjusting its oxidation state to suppress the local ring currents of its components.The discovery of ring currents around a molecule with a circumference of 7.5 nanometres, at room temperature, shows that quantum coherence can persist in surprisingly large molecular frameworks.

Identifiers

PMID27992878

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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.