Abstract

AbstractRings of porphyrins mimic natural light‐harvesting chlorophyll arrays and offer insights into electronic delocalization, providing a motivation for creating larger nanorings with closely spaced porphyrin units. Here, we demonstrate the first synthesis of a macrocycle consisting entirely of 5,15‐linked porphyrins. This porphyrin octadecamer was constructed using a covalent six‐armed template, made by cobalt‐catalyzed cyclotrimerization of an H‐shaped tolan with porphyrin trimer ends. The porphyrins around the circumference of the nanoring were linked together by intramolecular oxidative meso‐meso coupling and partial β‐β fusion, to give a nanoring consisting of six edge‐fused zinc(II) porphyrin dimer units and six un‐fused nickel(II) porphyrins. STM imaging on a gold surface confirms the size and shape of the spoked 18‐porphyrin nanoring (calculated diameter: 4.7 nm).

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