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Demonstrates the catalytic activity of selenoxanthylium salts in organic reactions, highlighting their potential for low-energy technology.
The design of low energy organic photoredox catalysts relies predominantly on π-extended frameworks. Incorporation of selenium into the xanthylium core shifts absorption toward the red region relative to lighter chalcogens (O and S), enabling catalysis with 650 nm light-sources. Selenoxanthylium salts are low-energy-absorbing organic photocatalysts with defined excited-state topology, distinguishing locally excited and charge-transfer states. Incorporation of a heavier chalcogen constitutes a design principle complementary to extended π-frameworks commonly used in organic photocatalysts. Under red-light irradiation, the catalysts engage in reductive quenching and operate on up to 5.0 mmol scale. Catalytic activity is demonstrated across multiple transformations, including [4 + 2] and [2 + 2] cycloadditions, C–H aminations, boronic acid oxidations, aza-Henry reactions, and trifluoromethylations.
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