Host (CdS)-guest (single-atomic Au) electron transfer mechanism for blue-LED-induced atom transfer radical addition of alkenes

被引:9
作者
Hao, Xiao-Li [1 ,2 ]
Chu, Xiao-Shan [2 ]
Luo, Ke-Ling [3 ]
Li, Wei [2 ]
机构
[1] Shaanxi Univ Technol, Sch Mat Sci & Engn, Natl & Local Joint Engn Lab Slag Comprehens Utiliz, Hanzhong 723000, Shaanxi, Peoples R China
[2] Shaanxi Univ Sci & Technol, Coll Chem & Chem Engn, Shaanxi Key Lab Chem Addit Ind, Xi'an 710021, Shaanxi, Peoples R China
[3] Shaanxi Univ Sci & Technol, Sch Arts & Sci, Xi'an 710021, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Single atomic gold; Atom transfer radical addition; Visible-light; Cadmium sulfide; Photocatalysis; CATALYST;
D O I
10.1016/j.jcat.2022.05.016
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Atom transfer radical addition (ATRA) is commonly applied to introduce perfluoroalkyl groups into organic molecules, but it often suffers from harsh reaction condition, poor yield and expensive catalyst usage for practical application. Light-induced ATRA reaction is of great significance due to its merits of mild reaction condition and easy operation, but it is generally difficult to achieve high yield because of the lack of ideal photosensitizers. Herein, an Au single-atom sites (SASs) decorated hexagonal cadmium sulfide (CdS) nanocatalyst (Cat(CdS-Au)) was synthesized to catalyze ATRA reaction under mild blue-LED-induction. As a result, the synergetic effect of CdS-Au interaction enhanced the optical properties and pro-moted the host (CdS)-guest (Au) electron transfer, leading to high ATRA yields (88-98%) and excellent selectivity even choosing different alkene substrates, which is remarkably superior over existing reaction systems (60-90% yields) ever reported in literatures. The present work sheds light on realizing high ATRA reaction yield via a green and high-efficient synthetic strategy. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:226 / 234
页数:9
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