Recent advances in cooperative N-heterocyclic carbenes and photocatalysis

Abstract

Radical chemistry has played an important role in organic synthetic chemistry in the past decades. Additionally, the combination of N-heterocyclic carbene (NHC) catalysis and photocatalysis involving radical processes has emerged as a powerful strategy for the synthesis of useful molecules. Thus, it has received significant attention and underwent significant development in recent years. In this review, we summarized the recent advances in this rapidly growing area of research from the perspective of reaction mechanisms through NHC-bound ketyl radicals generated via single-electron oxidation with an excited-state photocatalyst, single-electron reduction with a reduced-state photocatalyst or energy transfer (EnT) with an excited-state photocatalyst, followed by the SET process. In addition, the catalytic mechanisms, design and application of these reaction modes are discussed in detail.

Graphical abstract: Recent advances in cooperative N-heterocyclic carbenes and photocatalysis

Article information

Article type
Review Article
Submitted
27 Jul 2024
Accepted
07 Sep 2024
First published
25 Sep 2024

Org. Chem. Front., 2024, Advance Article

Recent advances in cooperative N-heterocyclic carbenes and photocatalysis

K. Tian, Z. Xia, J. Wei, H. Tao and X. Dong, Org. Chem. Front., 2024, Advance Article , DOI: 10.1039/D4QO01335B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements