Covalent Organic Frameworks toward Diverse Photocatalytic Aerobic Oxidations

被引:28
作者
Liu, Shuyang [1 ]
Tian, Miao [1 ]
Bu, Xiubin [1 ]
Tian, Hua [3 ,4 ]
Yang, Xiaobo [1 ,2 ]
机构
[1] Shenyang Normal Univ, Coll Chem & Chem Engn, Inst Catalysis Energy & Environm, Shenyang 110034, Peoples R China
[2] Tsinghua Univ, Dept Chem, Minist Educ, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, State Key Lab Bioact Subst & Funct Nat Med, Inst Mat Med, Beijing 100050, Peoples R China
[4] Chinese Acad Med Sci & Peking Union Med Coll, Beijing Key Lab Act Subst Discovery & Druggabill, Inst Mat Med, Beijing 100050, Peoples R China
关键词
aerobic oxidation; covalent organic frameworks; visible-light-driven; small organic molecules; DEHYDROGENATIVE-COUPLING REACTION; VISIBLE-LIGHT PHOTOCATALYSTS; METAL-FREE CATALYST; SINGLET-OXYGEN; C-H; SELECTIVE OXIDATION; ELECTRON-TRANSFER; CO2; REDUCTION; PHOTOREDOX CATALYSIS; EOSIN Y;
D O I
10.1002/chem.202100398
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photoactive two-dimensional covalent organic frameworks (2D-COFs) have become promising heterogenous photocatalysts in visible-light-driven organic transformations. Herein, a visible-light-driven selective aerobic oxidation of various small organic molecules by using 2D-COFs as the photocatalyst was developed. In this protocol, due to the remarkable photocatalytic capability of hydrazone-based 2D-COF-1 on molecular oxygen activation, a wide range of amides, quinolones, heterocyclic compounds, and sulfoxides were obtained with high efficiency and excellent functional group tolerance under very mild reaction conditions. Furthermore, benefiting from the inherent advantage of heterogenous photocatalysis, prominent sustainability and easy photocatalyst recyclability, a drug molecule (modafinil) and an oxidized mustard gas simulant (2-chloroethyl ethyl sulfoxide) were selectively and easily obtained in scale-up reactions. Mechanistic investigations were conducted using radical quenching experiments and in situ ESR spectroscopy, all corroborating the proposed role of 2D-COF-1 in photocatalytic cycle.
引用
收藏
页码:7738 / 7744
页数:7
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