| Literature DB >> 34260804 |
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.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