Casademont-Reig Irene, Guerrero-Avilés Raúl, Ramos-Cordoba Eloy, Torrent-Sucarrat Miquel, Matito Eduard
Donostia International Physics Center (DIPC), 20018, Donostia, Euskadi, Spain.
Polimero eta Material Aurreratuak: Fisika, Kimika eta Teknologia, Kimika Fakultatea, Euskal Herriko Unibertsitatea UPV/EHU, P.K. 1072, 20080, Donostia, Euskadi, Spain.
Angew Chem Int Ed Engl. 2021 Nov 2;60(45):24080-24088. doi: 10.1002/anie.202108997. Epub 2021 Aug 12.
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 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.
具有持续电流的大共轭环是分子尺度电子学中新型的有前景的结构。最近合成了一种据称维持着涉及78个π电子的芳香环电流的六卟啉纳米环结构。我们在此提供了令人信服的证据,表明该分子并非芳香性的,这与从存在较大离域误差的¹H-NMR数据和计算计算分析中推断的结果相反。这些纳米环中不存在芳香环电流的主要原因是从卟啉到桥连丁二炔连接体的转变中离域程度低,这破坏了整体共轭电路。这些结果突出了选择合适的计算方法来研究大共轭分子以及选择合适的芳香性描述符来识别导致芳香性丧失的分子部分的重要性。