光催化
光化学
化学
键裂
催化作用
纳米晶
可见光谱
电子转移
甲醛
材料科学
纳米技术
有机化学
光电子学
作者
Qiangwen Fan,Honglei Zhang,Dawei Liu,Chunpei Yan,Haibo Zhu,Zongbo Xie,Zhanggao Le
标识
DOI:10.1021/acs.joc.3c00653
摘要
Herein, we reported a facile and readily accessible visible-light-driven photocatalytic protocol to induce oxidative cleavage of C═C bonds to corresponding carbonyls using CsPbBr3 nanocrystals as photocatalysts. This catalytic system was applicable to a wide range of terminal and internal alkenes. Detailed mechanism studies indicated that a single-electron transfer (SET) process was involved in this transformation, wherein the superoxide radical (O2•-) and photogenerated holes played crucial roles. Additionally, DFT calculations revealed that the reaction was initiated by the addition of O2•- to the terminal carbon atom of the C═C bond and completed by releasing one molecular formaldehyde by the formed [2 + 2] intermediate; the latter conversion was a rate-determining process.
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