化学
光催化
电化学
催化作用
激进的
有机合成
光化学
离子键合
组合化学
纳米技术
氧化还原
有机化学
光催化
电极
物理化学
离子
材料科学
作者
Nicholas E. S. Tay,Dan Lehnherr,Tomislav Rovis
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2021-11-09
卷期号:122 (2): 2487-2649
被引量:292
标识
DOI:10.1021/acs.chemrev.1c00384
摘要
Redox processes are at the heart of synthetic methods that rely on either electrochemistry or photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both approaches provide access to high energy intermediates (e.g., radicals) that enable bond formations not constrained by the rules of ionic or 2 electron (e) mechanisms. Instead, they enable 1e mechanisms capable of bypassing electronic or steric limitations and protecting group requirements, thus enabling synthetic chemists to disconnect molecules in new and different ways. However, while providing access to similar intermediates, electrochemistry and photoredox catalysis differ in several physical chemistry principles. Understanding those differences can be key to designing new transformations and forging new bond disconnections. This review aims to highlight these differences and similarities between electrochemistry and photoredox catalysis by comparing their underlying physical chemistry principles and describing their impact on electrochemical and photochemical methods.
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