电子转移
化学
超快激光光谱学
反应性(心理学)
光化学
激发态
机制(生物学)
敏化
反应机理
生化工程
组合化学
光谱学
催化作用
有机化学
物理
神经科学
原子物理学
医学
替代医学
病理
量子力学
工程类
生物
作者
Max Coles,Gina Quach,Jonathon E. Beves,Evan G. Moore
标识
DOI:10.1002/anie.201916359
摘要
The development of photocatalytic reactions has provided many novel opportunities to expand the scope of synthetic organic chemistry. In parallel with progress towards uncovering new reactivity, there is consensus that efforts focused on providing detailed mechanistic insight in order to uncover underlying excited-state reactions are essential to maximise formation of desired products. With this in mind, we have investigated the recently reported sensitization-initiated electron transfer (SenI-ET) reaction for the C-H arylation of activated aryl halides. Using a variety of techniques, and in particular nanosecond transient absorption spectroscopy, we are able to distinguish several characteristic signals from the excited-state species involved in the reaction, and subsequent kinetic analysis under various conditions has facilitated a detailed insight into the likely reaction mechanism.
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