Cargando…
How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring
Large conjugated rings with persistent currents are novel promising structures in molecular‐scale electronics. A six‐porphyrin nanoring structure that allegedly sustained an aromatic ring current involving 78π electrons was recently synthesized. We provide here compelling evidence that this molecule...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596448/ https://www.ncbi.nlm.nih.gov/pubmed/34260804 http://dx.doi.org/10.1002/anie.202108997 |
_version_ | 1784600381596106752 |
---|---|
author | Casademont‐Reig, Irene Guerrero‐Avilés, Raúl Ramos‐Cordoba, Eloy Torrent‐Sucarrat, Miquel Matito, Eduard |
author_facet | Casademont‐Reig, Irene Guerrero‐Avilés, Raúl Ramos‐Cordoba, Eloy Torrent‐Sucarrat, Miquel Matito, Eduard |
author_sort | Casademont‐Reig, Irene |
collection | PubMed |
description | Large conjugated rings with persistent currents are novel promising structures in molecular‐scale electronics. A six‐porphyrin nanoring structure that allegedly sustained an aromatic ring current involving 78π electrons was recently synthesized. We provide here compelling evidence that this molecule is not aromatic, contrary to what was inferred from the analysis of (1)H‐NMR data and computational calculations that suffer from large delocalization errors. The main reason behind the absence of an aromatic ring current in these nanorings is the low delocalization in the transition from the porphyrins to the bridging butadiyne linkers, which disrupts the overall conjugated circuit. These results highlight the importance of choosing a suitable computational method to study large conjugated molecules and the appropriate aromaticity descriptors to identify the part of the molecule responsible for the loss of aromaticity. |
format | Online Article Text |
id | pubmed-8596448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85964482021-11-22 How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring Casademont‐Reig, Irene Guerrero‐Avilés, Raúl Ramos‐Cordoba, Eloy Torrent‐Sucarrat, Miquel Matito, Eduard Angew Chem Int Ed Engl Research Articles Large conjugated rings with persistent currents are novel promising structures in molecular‐scale electronics. A six‐porphyrin nanoring structure that allegedly sustained an aromatic ring current involving 78π electrons was recently synthesized. We provide here compelling evidence that this molecule is not aromatic, contrary to what was inferred from the analysis of (1)H‐NMR data and computational calculations that suffer from large delocalization errors. The main reason behind the absence of an aromatic ring current in these nanorings is the low delocalization in the transition from the porphyrins to the bridging butadiyne linkers, which disrupts the overall conjugated circuit. These results highlight the importance of choosing a suitable computational method to study large conjugated molecules and the appropriate aromaticity descriptors to identify the part of the molecule responsible for the loss of aromaticity. John Wiley and Sons Inc. 2021-08-12 2021-11-02 /pmc/articles/PMC8596448/ /pubmed/34260804 http://dx.doi.org/10.1002/anie.202108997 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Casademont‐Reig, Irene Guerrero‐Avilés, Raúl Ramos‐Cordoba, Eloy Torrent‐Sucarrat, Miquel Matito, Eduard How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring |
title | How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring
|
title_full | How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring
|
title_fullStr | How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring
|
title_full_unstemmed | How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring
|
title_short | How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring
|
title_sort | how aromatic are molecular nanorings? the case of a six‐porphyrin nanoring |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596448/ https://www.ncbi.nlm.nih.gov/pubmed/34260804 http://dx.doi.org/10.1002/anie.202108997 |
work_keys_str_mv | AT casademontreigirene howaromaticaremolecularnanoringsthecaseofasixporphyrinnanoring AT guerreroavilesraul howaromaticaremolecularnanoringsthecaseofasixporphyrinnanoring AT ramoscordobaeloy howaromaticaremolecularnanoringsthecaseofasixporphyrinnanoring AT torrentsucarratmiquel howaromaticaremolecularnanoringsthecaseofasixporphyrinnanoring AT matitoeduard howaromaticaremolecularnanoringsthecaseofasixporphyrinnanoring |