Synthesis of triple stranded porphyrin nanobelts

Molecular nanobelts are fascinating analogs of carbon nanotubes. Their rigid geometries and strongly coupled π-electrons have the potential to generate a wave function resembling that of a quantum ring. Here, we report the synthesis of triple stranded nanobelts consisting of 8 to 12 edge-fused porphyrin units with diameters of 21 to 32 angstroms. We synthesized these nanobelts by nickel-mediated coupling of <i>meso</i>-bromoporphyrins to form singly linked nanorings, followed by oxidation with gold(III) chloride. Experimental <sup>1</sup>H nuclear magnetic resonance spectra, supported by computational simulations, revealed that belts containing odd numbers of porphyrins, with circuits of 90 or 110 π-electrons, display global aromatic ring currents, whereas even-numbered belts, with 80, 100, or 120 π-electrons, are globally antiaromatic.

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Publication Details

Journal
Science
Published
2025-10-16
DOI
https://doi.org/10.1126/science.adz8900
Citations
6
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
3.11
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article

Synthesis of triple stranded porphyrin nanobelts

Wojciech Stawski, Arnau Rodríguez-Rubio, Janko Hergenhahn, Henrik Gotfredsen et al.
6 citations
Science
Porphyrin and Phthalocyanine Chemistry
3.11
article

Synthesis of triple stranded porphyrin nanobelts

Wojciech Stawski, Arnau Rodríguez-Rubio, Janko Hergenhahn, Henrik Gotfredsen, Matthew Edmondson, Joshua L. Field, James N. O’Shea, Harry L. Anderson, Alex Saywell, Igor Rončević, He Zhu, Prakhar Gupta, Ka Man Cheung, Joseph Straw, Lene Gödde
article en
6 citations

Abstract

Molecular nanobelts are fascinating analogs of carbon nanotubes. Their rigid geometries and strongly coupled π-electrons have the potential to generate a wave function resembling that of a quantum ring. Here, we report the synthesis of triple stranded nanobelts consisting of 8 to 12 edge-fused porphyrin units with diameters of 21 to 32 angstroms. We synthesized these nanobelts by nickel-mediated coupling of <i>meso</i>-bromoporphyrins to form singly linked nanorings, followed by oxidation with gold(III) chloride. Experimental <sup>1</sup>H nuclear magnetic resonance spectra, supported by computational simulations, revealed that belts containing odd numbers of porphyrins, with circuits of 90 or 110 π-electrons, display global aromatic ring currents, whereas even-numbered belts, with 80, 100, or 120 π-electrons, are globally antiaromatic.

ScienceVol. 390(6770)
University of Nottingham (GB), Universität Ulm (DE), University of Manchester (GB), University of Oxford (GB)
Openalex Percentile: Top 8%
Porphyrin and Phthalocyanine Chemistry
3.11
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Synthesis of triple stranded porphyrin nanobelts — Wojciech Stawski, Arnau Rodríguez-Rubio, et al. · Science (2025) | TGRS Research Map | TGRS