Xu Yang, Mu Bo-Shuai, Tu Zhiyu, Liang Weiqiu, Li Jiahao, Sang Ziyang, Liu Zhibo
Beijing National Laboratory for Molecular Sciences, Radiochemistry and Radiation Chemistry Key Laboratory of Fundamental Science, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering, Peking University Beijing 100871 China
Peking University-Tsinghua University Center for Life Sciences, Peking University Beijing 100871 China.
Chem Sci. 2024 Dec 23;16(4):1867-1875. doi: 10.1039/d4sc05558f. eCollection 2025 Jan 22.
Oxidation is a fundamental transformation in synthesis. Developing facile and effective aerobic oxidation processes under ambient conditions is always in high demand. Benefiting from its high energy and good penetrability, ionizing radiation can readily produce various reactive species to trigger chemical reactions, offering another option for synthesis. Here, we report an ionizing radiation-induced aerobic oxidation strategy to synthesize oxygen-containing compounds. We discovered that molecular oxygen (O) could be activated by reactive particles generated from solvent radiolysis to produce solvent-derived peroxyl radicals (ROO·), which facilitated the selective oxidation of sulfides and phosphorus(iii) compounds at room temperature without catalysts. Density functional theory (DFT) calculations further revealed that multiple ROO· enable the oxidation reaction through an oxygen atom transfer process. This aerobic oxidation strategy broadens the research scope of radiation-induced chemical transformations while offering an opportunity to convert nuclear energy into chemical energy.
氧化是合成中的一种基本转化。在环境条件下开发简便有效的需氧氧化过程一直是人们的迫切需求。得益于其高能量和良好的穿透性,电离辐射能够轻易地产生各种活性物种以引发化学反应,为合成提供了另一种选择。在此,我们报道一种电离辐射诱导的需氧氧化策略来合成含氧化合物。我们发现分子氧(O)可被溶剂辐射分解产生的活性粒子激活,生成溶剂衍生的过氧自由基(ROO·),这使得在室温下无需催化剂就能促进硫化物和磷(III)化合物的选择性氧化。密度泛函理论(DFT)计算进一步表明,多个ROO·通过氧原子转移过程实现氧化反应。这种需氧氧化策略拓宽了辐射诱导化学转化的研究范围,同时为将核能转化为化学能提供了契机。