Eosin Y Catalyzed Photochemical Synthesis of Arylated Phenothiazones.

In the presence of Eosin Y (EY), the synthesis of substituted phenothiazones was carried out efficiently using various substituted 2-aminothiophenol, diazonium salts, and 1,4-napthaquinones (1,4-NQ) at room temperature (RT) (condition: green LED of 525 nm, 44 W; reaction time: 8 h, isolated yield: 68-90%). A fluorescence quenching experiment and density functional theory (DFT) calculations suggested that the triplet photoexcited state of EY (EY*; τT = 320 ± 10 ns) converts to EY+• via oxidative quenching by ArN2 + (-1.11 V vs SCE for EY* to EY+•) initially. Thiyl and aryl radicals were captured as TEMPO adducts in high-resolution mass spectroscopy (HRMS). The reaction was not inhibited by the addition of a singlet oxygen quencher such as 1,4-diazobicyclo [2.2.2] octane (DABCO), which suggests that singlet oxygen is not participated. © 2024 The Authors. Published by American Chemical Society.

Citation

Bhawana Nagar, Sarban Kumar Yadav, Naiwrit Karmodak, Basab Bijayi Dhar. Eosin Y Catalyzed Photochemical Synthesis of Arylated Phenothiazones. ACS omega. 2024 Aug 20;9(33):35458-35462

PMID: 39184487

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