Issue 9, 2022

The advent and development of organophotoredox catalysis

Abstract

In the last decade, photoredox catalysis has unlocked unprecedented reactivities in synthetic organic chemistry. Seminal advancements in the field have involved the use of well-studied metal complexes as photoredox catalysts (PCs). More recently, the synthetic community, looking for more sustainable approaches, has been moving towards the use of purely organic molecules. Organic PCs are generally cheaper and less toxic, while allowing their rational modification to an increased generality. Furthermore, organic PCs have allowed reactivities that are inaccessible by using common metal complexes. Likewise, in synthetic catalysis, the field of photocatalysis is now experiencing a green evolution moving from metal catalysis to organocatalysis. In this feature article, we discuss and critically comment on the scientific reasons for this ongoing evolution in the field of photoredox catalysis, showing how and when organic PCs can efficiently replace their metal counterparts.

Graphical abstract: The advent and development of organophotoredox catalysis

Article information

Article type
Feature Article
Submitted
17 Հկտ 2021
Accepted
10 Դկտ 2021
First published
10 Դկտ 2021

Chem. Commun., 2022,58, 1263-1283

The advent and development of organophotoredox catalysis

T. Bortolato, S. Cuadros, G. Simionato and L. Dell’Amico, Chem. Commun., 2022, 58, 1263 DOI: 10.1039/D1CC05850A

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