光催化
催化作用
量子点
可见光谱
光化学
化学
氧化磷酸化
键裂
氧化裂解
劈理(地质)
纳米技术
材料科学
有机化学
光电子学
复合材料
生物化学
断裂(地质)
作者
Jianing Li,Jingnan Zhao,Cunfei Ma,Zongyi Yu,Hongfei Zhu,Lei Yun,Qingwei Meng
出处
期刊:Chemsuschem
[Wiley]
日期:2021-09-08
卷期号:14 (22): 4985-4992
被引量:9
标识
DOI:10.1002/cssc.202101504
摘要
Abstract The oxidative cleavage of C=C bonds is an important chemical reaction, which is a popular reaction in the photocatalytic field. However, high catalyst‐loading and low turnover number (TON) are general shortcomings in reported visible‐light‐driven reactions. Herein, the direct oxidative cleavage of C=C bonds through water‐soluble CdSe quantum dots (QDs) is described under visible‐light irradiation at room temperature with high TON (up to 3.7×10 4 ). Under the same conditions, water‐soluble CdSe QDs could also oxidize sulfides to sulfoxides with 51–84 % yields and TONs up to 3.4×10 4 . The key features of this photocatalytic protocol include high TONs, wide substrates scope, low catalyst loadings, simple and mild reaction conditions, and molecular O 2 as the oxidant.
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