One-Pot Synthesis of Triazatriphenylene Using the Povarov Reaction

The Povarov reaction combines aromatic amines, aldehydes, and alkynes in a single step and is regarded as an annulative p-extension reaction of aromatic amines. In this study, the Povarov reaction was investigated as an efficient tool for the synthesis of aza-polycyclic aromatic hydrocarbons via multiple p-extensions. The double Povarov reaction of 1,4-diaminobenzene yielded the 4,7-phenanthroline derivative as the major product, regardless of the steric repulsion in the product. The site selectivity mainly depended on the HOMO distribution of the intermediate rather than the steric factor. Based on these insights, a 1,5,9-triazatriphenylene derivative was synthesized via a triple Povarov reaction. The structures of the synthesized compounds were unambiguously determined by single-crystal X-ray diffraction analysis. The triazatriphenylene derivative formed a smooth and stable thin film upon vacuum vapor deposition and served as a hole-blocking material in organic light-emitting diodes.

Automated summary

The Povarov reaction is an efficient tool for the synthesis of aza-polycyclic aromatic hydrocarbons, with site selectivity depending on the HOMO distribution of the intermediate. Specific molecular structures can be synthesized through the Povarov reaction, with one derivative showing good performance as a hole-blocking material in organic light-emitting diodes.