ArticleNature2017
Aromatic and antiaromatic ring currents in a molecular nanoring.
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.
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Who cites it
53 citing papers in PubMed.
- Decoding Chemical Resonance in π‑Conjugated Systems.ACS physical chemistry Au · 2026Article
- Redox- and protonation-driven Baird and Clar aromaticity in asymmetric multicyclic octaphyrins.Chemical science · 2026Article
- An 18-Porphyrin Nanoring at the Size Limit for Global Aromaticity.Journal of the American Chemical Society · 2025Article
- A Review of On-Surface Synthesis and Characterization of Macrocycles.Nanomaterials (Basel, Switzerland) · 2025Review
- Strong Ferromagnetic Coupling between Co and CoThe journal of physical chemistry. A · 2025Article
- Article
- Redox-Switchable Aromaticity in a Helically Extended Indeno[2,1-Journal of the American Chemical Society · 2024Article
- SynergisticChemical science · 2024Article
- Possibility of persistent current in S-states.Scientific reports · 2024Article
- Probing the Antiaromaticity and Coordination Chemistry of Bowl-Shaped Zinc(II) Norcorrole.Inorganic chemistry · 2024Article
- Molecular Pseudorotation in Phthalocyanines as a Tool for Magnetic Field Control at the Nanoscale.Journal of the American Chemical Society · 2024Article
- DNA as a perfect quantum computer based on the quantum physics principles.Scientific reports · 2024Article
- Antiaromatic Molecules as Magnetic Couplers: A Computational Quest.The journal of physical chemistry. A · 2024Article
- Dynamic covalent synthesis.Chemical science · 2024Review
- A dodecamethoxy[6]cycloparaphenylene consisting entirely of hydroquinone ethers: unveiling in-plane aromaticity through a rotaxane structure.Nature communications · 2023Article
- Current-Density Calculations on Zn-PorphyrinThe journal of physical chemistry. A · 2023Article
- Tetra-tert-butyl-s-indacene is a Bond-Localized CAngewandte Chemie (International ed. in English) · 2023Article
- Substituent effects on paratropicity and diatropicity in π-extended hexapyrrolohexaazacoronene.Chemical science · 2023Article
- Aromaticity: Quo Vadis.Chemical science · 2023Review
- β,β-Directly Linked Porphyrin Rings: Synthesis, Photophysical Properties, and Fullerene Binding.Journal of the American Chemical Society · 2023Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
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.
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27992878What OpenQuestion holds
Registered trials
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.