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光氧化还原催化可收集多个光子或电化学能量。

Photoredox catalysis harvesting multiple photon or electrochemical energies.

作者信息

Lepori Mattia, Schmid Simon, Barham Joshua P

机构信息

Fakultät für Chemie und Pharmazie, Universität Regensburg, Universitatsstraße 31, 93040 Regensburg, Germany.

出版信息

Beilstein J Org Chem. 2023 Jul 28;19:1055-1145. doi: 10.3762/bjoc.19.81. eCollection 2023.

DOI:10.3762/bjoc.19.81
PMID:37533877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10390843/
Abstract

Photoredox catalysis (PRC) is a cutting-edge frontier for single electron-transfer (SET) reactions, enabling the generation of reactive intermediates for both oxidative and reductive processes via photon activation of a catalyst. Although this represents a significant step towards chemoselective and, more generally, sustainable chemistry, its efficacy is limited by the energy of visible light photons. Nowadays, excellent alternative conditions are available to overcome these limitations, harvesting two different but correlated concepts: the use of multi-photon processes such as consecutive photoinduced electron transfer (conPET) and the combination of photo- and electrochemistry in synthetic photoelectrochemistry (PEC). Herein, we review the most recent contributions to these fields in both oxidative and reductive activations of organic functional groups. New opportunities for organic chemists are captured, such as selective reactions employing super-oxidants and super-reductants to engage unactivated chemical feedstocks, and scalability up to gram scales in continuous flow. This review provides comparisons between the two techniques (multi-photon photoredox catalysis and PEC) to help the reader to fully understand their similarities, differences and potential applications and to therefore choose which method is the most appropriate for a given reaction, scale and purpose of a project.

摘要

光氧化还原催化(PRC)是单电子转移(SET)反应的前沿领域,通过催化剂的光子活化,能够为氧化和还原过程生成反应中间体。尽管这代表了朝着化学选择性以及更广泛的可持续化学迈出的重要一步,但其功效受到可见光光子能量的限制。如今,有出色的替代条件可克服这些限制,融合了两个不同但相关的概念:使用多光子过程,如连续光致电子转移(conPET),以及在合成光电化学(PEC)中将光化学与电化学相结合。在此,我们综述了这些领域在有机官能团氧化和还原活化方面的最新贡献。捕捉到了有机化学家的新机遇,例如采用超氧化剂和超还原剂进行选择性反应以处理未活化的化学原料,以及在连续流中扩大至克级规模。本综述对这两种技术(多光子光氧化还原催化和PEC)进行了比较,以帮助读者充分理解它们的异同及潜在应用,从而选择最适合特定反应、规模和项目目的的方法。

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