Visible-Light Photocatalysis: Does It Make a Difference in Organic Synthesis?

被引:1615
|
作者
Marzo, Leyre [1 ]
Pagire, Santosh K. [1 ]
Reiser, Oliver [1 ]
Koenig, Burkhard [1 ]
机构
[1] Univ Regensburg, Inst Organ Chem, Univ Str 31, D-93053 Regensburg, Germany
关键词
cross-coupling; cycloadditions; photocatalysis; radical reactions; visible light; CROSS-COUPLING REACTIONS; PALLADIUM-CATALYZED ARYLATION; TRANSFER RADICAL-ADDITION; C-H ARYLATION; SINGLE-ELECTRON TRANSMETALATION; ANTI-MARKOVNIKOV HYDROAMINATION; ENANTIOSELECTIVE ALPHA-ALKYLATION; SELECTIVE AROMATIC CHLORINATION; TRANSFER CYCLIZATION REACTIONS; TRANSITION-METAL CATALYSIS;
D O I
10.1002/anie.201709766
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Visible-light photocatalysis has evolved over the last decade into a widely used method in organic synthesis. Photocatalytic variants have been reported for many important transformations, such as cross-coupling reactions, -amino functionalizations, cycloadditions, ATRA reactions, or fluorinations. To help chemists select photocatalytic methods for their synthesis, we compare in this Review classical and photocatalytic procedures for selected classes of reactions and highlight their advantages and limitations. In many cases, the photocatalytic reactions proceed under milder reaction conditions, typically at room temperature, and stoichiometric reagents are replaced by simple oxidants or reductants, such as air, oxygen, or amines. Does visible-light photocatalysis make a difference in organic synthesis? The prospect of shuttling electrons back and forth to substrates and intermediates or to selectively transfer energy through a visible-light-absorbing photocatalyst holds the promise to improve current procedures in radical chemistry and to open up new avenues by accessing reactive species hitherto unknown, especially by merging photocatalysis with organo- or metal catalysis.
引用
收藏
页码:10034 / 10072
页数:39
相关论文
共 50 条
  • [21] Pyrene-based porous organic framework for efficient heterogeneous visible-light photocatalysis
    Lu, Jingzhi
    Zhang, Jian
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [22] Band engineering of ZnS by codoping for visible-light photocatalysis
    Wan, Hui
    Xu, Liang
    Huang, Wei-Qing
    Huang, Gui-Fang
    He, Chao-Ni
    Zhou, Jia-Hui
    Peng, P.
    APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 2014, 116 (02): : 741 - 750
  • [23] Bioorthogonal Synthetic Chemistry Enabled by Visible-Light Photocatalysis
    Mato, Mauro
    Fernandez-Gonzalez, Xulian
    DAvino, Cinzia
    Tomas-Gamasa, Maria
    Mascarenas, Jose L.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2024, 63 (47)
  • [24] Visible-light photocatalysis of ZnO deposited on nanoporous Au
    Masataka Hakamada
    Motohiro Yuasa
    Takashi Yoshida
    Fumi Hirashima
    Mamoru Mabuchi
    Applied Physics A, 2014, 114 : 1061 - 1066
  • [25] Hydrodifluoromethylation of unactivated alkenes enabled by Visible-Light Photocatalysis
    Jha, Avishek Kumar
    Kumar, Vivek
    Perumandla, Sanjay Kumar
    Yatham, Veera Reddy
    CHEMPHOTOCHEM, 2024, 8 (06)
  • [26] Visible-light photocatalysis in doped titanium oxides.
    Asahi, R
    Morikawa, T
    Taga, Y
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2001, 222 : U633 - U633
  • [27] Integrating TEMPO and Its Analogues with Visible-Light Photocatalysis
    Lang, Xianjun
    Zhao, Jincai
    CHEMISTRY-AN ASIAN JOURNAL, 2018, 13 (06) : 599 - 613
  • [28] Visible-light photocatalysis of ZnO deposited on nanoporous Au
    Hakamada, Masataka
    Yuasa, Motohiro
    Yoshida, Takashi
    Hirashima, Fumi
    Mabuchi, Mamoru
    APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 2014, 114 (04): : 1061 - 1066
  • [29] A Dual Plasmonic Photoelectrode System for Visible-Light Photocatalysis
    Nishi, Hiroyasu
    Miyake, Koji
    Kao, Kun-Che
    Tatsuma, Tetsu
    CHEMNANOMAT, 2020, 6 (04) : 529 - 532
  • [30] Increasing visible-light absorption for photocatalysis with black BiOCl
    Ye, Liqun
    Deng, Kejian
    Xu, Feng
    Tian, Lihong
    Peng, Tianyou
    Zan, Ling
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2012, 14 (01) : 82 - 85