Literature DB >> 34260804

How aromatic are molecular nanorings? The case of a six-porphyrin nanoring†.

Eduard Matito1, Irene Casademont2, Eloy Ramos-Cordoba2, Miquel Torrent-Sucarrat2, Raúl Guerrero-Avilés3.   

Abstract

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 synthesize. In this paper, we provide compelling evidence that this molecule is not aromatic, contrary to what was inferred from the analysis of 1H-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.
© 2021 Wiley-VCH GmbH.

Entities:  

Keywords:  aromaticity; delocalization error; magnetic properties; nanoring; quantum chemistry

Year:  2021        PMID: 34260804     DOI: 10.1002/anie.202108997

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Aromaticity and Extrusion of Benzenoids Linked to [o-COSAN]- : Clar Has the Answer.

Authors:  Jordi Poater; Clara Viñas; David Olid; Miquel Solà; Francesc Teixidor
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-29       Impact factor: 16.823

  1 in total

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