Lasky Matthew R, Liu En-Chih, Remy Matthew S, Sanford Melanie S
Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 48109, United States.
Corporate R&D, Dow, 1776 Building, Midland, Michigan 48667, United States.
J Am Chem Soc. 2024 May 29;146(21):14799-14806. doi: 10.1021/jacs.4c02991. Epub 2024 May 17.
This report describes the development of a visible-light photocatalytic system for C(sp)-H amination that leverages -generated photocatalysts. We demonstrate that the combination of acridine derivatives and Lewis acids forms potent photooxidants that promote the C-H amination of electronically diverse arenes upon irradiation with visible-light (440 nm). A first-generation photocatalyst composed of Sc(OTf) and acridine effects the C-H amination of substrates with oxidation potentials ≤ +2.5 V vs SCE with pyrazole, triazole, and pyridine nucleophiles. Furthermore, the simplicity and modularity of this system enable variation of both Lewis acid and acridine to tune reactivity. This enabled the rapid identification of two second-generation photocatalysts (derived from (i) Al(OTf) and acridine or (ii) Sc(OTf) and a pyridinium-substituted acridine) that catalyze a particularly challenging transformation: C(sp)-H amination with benzene as the limiting reagent.
本报告描述了一种利用原位生成的光催化剂实现C(sp)-H胺化的可见光光催化体系的开发。我们证明,吖啶衍生物与路易斯酸的组合形成了强效光氧化剂,在用可见光(440 nm)照射时能促进电子性质各异的芳烃的C-H胺化反应。由Sc(OTf)₃和吖啶组成的第一代光催化剂可实现底物与吡唑、三唑和吡啶亲核试剂的C-H胺化反应,这些底物的氧化电位相对于饱和甘汞电极(SCE)≤ +2.5 V。此外,该体系的简单性和模块化使得路易斯酸和吖啶都能发生变化以调节反应活性。这使得能够快速鉴定出两种第二代光催化剂(分别衍生自(i)Al(OTf)₃和吖啶或(ii)Sc(OTf)₃和吡啶取代的吖啶),它们能催化一种特别具有挑战性的转化反应:以苯作为限量试剂的C(sp)-H胺化反应。