催化作用
活动站点
氧化剂
铜
活动中心
合理设计
产量(工程)
活性氧
惰性
吸附
化学
无机化学
材料科学
纳米技术
物理化学
有机化学
冶金
作者
Yu Xiong,Shibin Wang,Wenxing Chen,Jian Zhang,Qiheng Li,Han‐Shi Hu,Lirong Zheng,Wensheng Yan,Lin Gu,Dingsheng Wang,Yadong Li
出处
期刊:Small
[Wiley]
日期:2021-02-01
卷期号:17 (8)
被引量:52
标识
DOI:10.1002/smll.202006834
摘要
Abstract Clear recognition and rational construction of suitable active center for specific reaction is always of great significance in designing highly efficient catalysts. Herein, a dual‐active‐site copper catalyst (DAS‐Cu) containing both CuN 3 and CuN 4 sites is reported. Such catalysts show extremely high catalytic performance (yield: up to 97%) toward oxyphosphorylation of alkenes, while catalysts with single active site (CuN 3 or CuN 4 ) are chemically inert in this reaction. Combined with theoretical and experimental results, the different roles of two different Cu active sites in this reaction are further identified. CuN 3 site captures the oxygen and trigger further oxidizing process, while CuN 4 site provides moderate adsorption sites for the protection of phosphonyl radicals. This work deeply discloses the significant cooperated role with two single‐atomic sites in one catalytic active center and brings up a valuable clue for the rational design of better‐performing heterogeneous catalyst.
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