Accelerated photochemical reactions at oil-water interface exploiting melting point depression

• 成果类型: Article
• 署名作者: Tian, Ya-Ming; Silva, Wagner; Gschwind, Ruth M.; Koenig, Burkhard
• 署名单位: University of Regensburg
• 刊物名称: SCIENCE
• ISSN/ISSBN: 0036-9614
• DOI: 10.1126/science.adl3092
• 发表日期: 2024-02-16
• 页码: 750-756
• 关键词: organic-reactions; chemical-shifts; spectroscopy; amination; heterocycles; orientation; alkylation; complexes; DISCOVERY; chemistry

摘要

Water can accelerate a variety of organic reactions far beyond the rates observed in classical organic solvents. However, using pure water as a solvent introduces solubility constraints that have limited the applicability of efficient photochemistry in particular. We report here the formation of aggregates between pairs of arenes, heteroarenes, enamines, or esters with different electron affinities in an aqueous medium, leading to an oil-water phase boundary through substrate melting point depression. The active hydrogen atoms in the reactants engage in hydrogen bonds with water, thereby accelerating photochemical reactions. This methodology realizes appealingly simple conditions for aqueous coupling reactions of complex solid molecules, including complex drug molecules that are poorly soluble in water.