Photocatalytic water splitting converts solar energy to storable hydrogen molecules which has the highest energy per mass. Most catalysts for photocatalytic water splitting utilize noble metals or precious metals. Organic photocatalysts are attracting more attention owing to several advantages like light weight, low cost, defined structure and tunability. In this study, the synthesis of several dibenzo[b,f][1,5]- diazocines via microwave irradiation for water splitting application is reported. Microwave irradiation facilitates fast, safe and simple synthesis in green reaction conditions. Mini library of dibenzo[b,f][1,5]diazocines were created in order to understand substituents effect on the photocatalytic activity.

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Robinson′s synthesis has long been a classic in organic chemistry due to its simplicity and impact in the industry. Various modifications have been made to improve the system. Among them, replacing acetone with more acidic chemical equivalents such as calcium dicarboxylic acid or ethyl dicarboxylic acetone improved the yield. In line with this trend, our group previously reported the synthesis of mono- and di-N-substituted tropinone derivatives from the one-pot reaction of 2,5-dimethoxy tetrahydrofuran and various amines with acetonedicarboxylic acid in the presence of HCl and water at room temperature. In this study, the synthesis with acetone instead of acetone-dicarboxylic acid was examined. Mono- and di-N-substituted nortropinones were prepared in higher yields in all cases although there were extent to which yields increased depending on the nature of substituents