Abstract

Aromaticity can be defined by the ability of a molecule to sustain a ring current when placed in a magnetic field. Hückel’s rule states that molecular rings with [4n+2] π-electrons are aromatic, with an induced magnetisation that opposes the external field inside the ring, whereas those with 4n π-electrons are antiaromatic, with the opposite magnetisation. This rule reliably predicts the behaviour of small molecules, typically with fewer than 22 π-electrons (n = 5). It is not clear whether aromaticity has a size limit, or whether Hückel’s rule extends to much larger macrocycles. Here, we present evidence for global aromaticity in porphyrin nanorings with circuits of up to 162 π-electrons (n = 40); aromaticity is controlled by changing the constitution, oxidation state and conformation. Whenever a ring current is observed, its direction is correctly predicted by Hückel’s rule. The largest ring currents occur when the porphyrins units have fractional oxidation states.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call