?-Expanded pyrazinoporphyrins for photocatalysis: How many rings are required?

A series of pi-expanded pyrazinoporphyrins were successfully prepared and tested as sensitizers for photocatalytic aerobic sulfides oxidation. 2,3-Diaminoporphyrin derivative was used as a key intermediate for the preparation of porphyrins fused with naphtho-, phenanthrene-, phenanthroline-and acenaphthoquinone fragments and the structures of the obtained compounds were proved by detailed analysis of NMR. The peculiarities and limitations of the condensation of diaminoporphyrin with a set of corresponding aromatic quinones were investigated. Gradual bathochromic shift of absorption bands was observed in the series of the prepared compounds, corre-lating with the gradual expansion of the macrocycle aromatic system. The photostability of the obtained pho-tosensitizers was tested prior to their application as photocatalysts. The photocatalytic performance of the obtained pi-expanded pyrazinoporphyrins was investigated in the aerobic oxidation of thioanisole and revealed the increase of the activity with the expansion of the pi-system of the molecule. Complete conversion of the substrate and over 98% selectivity was achieved with 10-2 mol% catalyst loading, that correspond to turnover number (TON) ca. 10,000. The maximal TON = 89,000 could be reached with 10-3 mol% catalyst loading. The measurements of the singlet oxygen generation quantum yields along with the DFT analysis of perturbation of the molecular orbitals of the photosensitizers was performed. The latter analysis revealed the presence of orbitals with predominant localization either at porphyrin macrocycle or at peripheral polyaromatic part of the molecule, allowing to expect charge separation upon photoexcitation.

Automated summary

A series of pi-expanded pyrazinoporphyrins were synthesized and tested as sensitizers for the photocatalytic oxidation of sulfides. The structures of the compounds were confirmed by NMR analysis. The absorption bands of the compounds showed a gradual bathochromic shift with the expansion of the macrocycle aromatic system. The photocatalytic activity of the pi-expanded pyrazinoporphyrins increased with the expansion of the pi-system, achieving high conversion and selectivity with low catalyst loading.