School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
School of Chemistry, University of New South Wales, Sydney, NSW, 2052, Australia.
Angew Chem Int Ed Engl. 2020 Jun 8;59(24):9522-9526. doi: 10.1002/anie.201916359. Epub 2020 Apr 7.
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.
光催化反应的发展为拓展合成有机化学的范围提供了许多新的机会。在揭示新反应性的同时,人们普遍认为,努力提供详细的机理见解以揭示潜在的激发态反应对于最大限度地形成所需产物是至关重要的。考虑到这一点,我们研究了最近报道的敏化引发的电子转移(SenI-ET)反应,用于活化芳基卤化物的 C-H 芳基化。使用各种技术,特别是纳秒瞬态吸收光谱,我们能够从反应中涉及的激发态物种中区分出几种特征信号,并且在各种条件下进行的后续动力学分析有助于深入了解可能的反应机理。