Abstract
What is the size limit for global aromaticity? How large can a macrocyclic π-system be and still exhibit an aromatic ring current around its circumference? We address this question by investigating a π-conjugated butadiyne-linked 18-porphyrin nanoring (diameter 8 nm). This nanoring was synthesized by two different strategies: classical template-directed synthesis, using a radial template with 18 pyridyl binding sites, and Vernier templating, using a small hexapyridyl template. Both strategies are effective when the porphyrins have octyloxy sidechains but classical templating is more effective than Vernier templating when the porphyrins have bulky trihexylsilyl substituents. The size and shape of the nanoring was confirmed by scanning tunnelling microscopy (STM). Nucleus-independent chemical shift (NICS) calculations using the BLYP35 functional predicted that the 18 porphyrin nanoring would show global aromaticity in the 10+ and 14+ oxidation states and antiaromaticity in the 12+ and 16+ oxidation state. There is also experimental evidence for weak global ring currents in this nanoring: 19F NMR oxidation titrations on the nanoring bound to a fluorinated template revealed shoulder signals indicating weak global aromatic and antiaromatic ring currents in the 10+ and 12+ oxidation states, which have Hückel circuits of 242 and 240 π-electrons, respectively. The ring currents in this 18-porphyrin ring are weaker than those in the homologous 12-porphyrin ring by at least a factor of two.
Supplementary materials
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Supporting Information
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Synthetic procedures and characterization data
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