Synthesis of Heptagon-Containing Polyarenes by Catalytic C-H Activation

Nanocarbons incorporating non-hexagonal aromatic rings - such as five-, seven-, and eight-membered rings - have various intriguing physical properties such as curved structures, unique one-dimensional packing, and promising magnetic, optical, and conductivity properties. Herein, we report an efficient synthetic approach to polycyclic aromatics containing seven-membered rings via a palladium-catalyzed intramolecular Ar-H/Ar-Br coupling. In addition to all-hydrocarbon scaffolds, heteroatom-embedded heptagon-containing polyarenes can be efficiently constructed with this method. Rhodium- and palladium-catalyzed sequential six- and seven-membered ring formations also afford complex heptagon-containing molecular nanocarbons from readily available arylacetylenes and biphenyl boronic acids. Detailed mechanistic analysis by DFT calculations showed the feasibility of seven-membered ring formation by a concerted metalation-deprotonation mechanism. This reaction can serve as a template for the synthesis of a wide range of seven-membered ring-containing molecular nanocarbons. Herein, we report an efficient synthetic method, involving a Pd-catalyzed intramolecular coupling, for polycyclic aromatic compounds containing seven-membered rings. A variety of heptagon-containing molecular nanocarbons were synthesized. In addition, a one-pot synthetic method comprising Rh-catalyzed annulation and Pd-catalyzed cyclization was developed. Furthermore, it was possible to construct two seven-membered rings simultaneously.image