Wang Yongtao, Zhou Yujia, Sun Wenjing, Wang Xinyu, Yao Jia, Li Haoran
Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou, 310058, China.
Center of Chemistry for Frontier Technologies, ZJU-NHU United R&D Center, Zhejiang University, 866 Yuhangtang Rd, Hangzhou, 310058, China.
Adv Sci (Weinh). 2024 Aug;11(29):e2402890. doi: 10.1002/advs.202402890. Epub 2024 May 29.
Copper-catalyzed C─H oxygenation has drawn considerable attention in mechanistic studies. However, a comprehensive investigation combining radical pathways with a metal-catalytic cycle is challenged by the intricate organic radicals and metallic intermediates. Herein, an online coupled EPR/UV-vis/near-IR detecting method is developed to simultaneously monitor both reactive radical species and copper complex intermediates during the reaction. Focusing on copper-catalyzed phenol oxygenation with cumene hydroperoxide, the short-lived alkylperoxyl radical (EPR signal at g = 2.0143) as well as the unexpected square planar Cu(II)-alkoxyl radical complex (near-IR signal at 833 nm) are unveiled during the reaction, in addition to the observable phenoxyl radical in EPR, quinone product in UV-vis, and Cu(II) center in EPR. With a comprehensive picture of diverse intermediates evolving over the same timeline, a novel Cu(I)/Cu(II) proposed relay-catalyzed sequential radical pathway. In this sequence, Cu(II) activates hydroperoxide through Cu(II)-OOR into the alkylperoxide radical, while the reaction between Cu(I) and hydroperoxide leads to Cu(II)(•OR)OH with high H-atom abstracting activity. These results provide a thorough understanding of the Cu(I)/Cu(II) relay catalysis for phenol oxygenation, setting the stage for mechanistic investigations into intricate radical reactions promoted by metallic complexes.
铜催化的C─H氧化反应在机理研究中引起了广泛关注。然而,将自由基途径与金属催化循环相结合的全面研究受到复杂的有机自由基和金属中间体的挑战。在此,开发了一种在线耦合的电子顺磁共振(EPR)/紫外可见光谱(UV-vis)/近红外光谱(near-IR)检测方法,以在反应过程中同时监测反应性自由基物种和铜配合物中间体。以铜催化的苯酚与氢过氧化异丙苯的氧化反应为重点,反应过程中除了在EPR中可观察到的苯氧自由基、UV-vis中的醌产物和EPR中的Cu(II)中心外,还揭示了短寿命的烷基过氧自由基(g = 2.0143处的EPR信号)以及意想不到的平面正方形Cu(II)-烷氧基自由基配合物(833 nm处的近红外信号)。通过全面了解在同一时间轴上演变的各种中间体,提出了一种新颖的Cu(I)/Cu(II)接力催化的连续自由基途径。在这个序列中,Cu(II)通过Cu(II)-OOR将氢过氧化物活化成烷基过氧自由基,而Cu(I)与氢过氧化物之间的反应产生具有高氢原子提取活性的Cu(II)(•OR)OH。这些结果为苯酚氧化反应的Cu(I)/Cu(II)接力催化提供了全面的理解,为深入研究金属配合物促进的复杂自由基反应的机理奠定了基础。