Advances of photocatalytic carboxylation of C(sp3)-H bond with CO2: A sustainable strategy for CO2 fixation

Abstract

Carbon dioxide (CO2) is well recognized as a sustainable C1 synthon for producing a variety of carboxylic acid derivatives, including important natural and synthetic amino acids. Despite its sustainability, the CO2 molecule's high thermodynamic stability and kinetic inertness pose significant challenges to its broader application in organic synthesis. In recent years, the inertness and high stability of the CO2 molecule have been successfully overcome through various stoichiometric and catalytic methods. Among these, visible-light-induced photoredox catalysis has emerged as a popular and effective approach, offering a greener and more sustainable solution. Various carboxylation reactions involving C(sp3)-H, C(sp2)-H, C(sp)-H, Ar-X have been successfully developed by using a suitable photocatalyst under visible light excitation. In this mini review, we explore recent progress in carboxylation reactions through the functionalization of C(sp3)–H bonds specifically in various organic molecules using molecular CO2 using photocatalysis including organo-photocatalysts, homogeneous photocatalysts and heterogeneous photocatalysts.

Article information

Article type
Critical Review
Submitted
03 Oct 2024
Accepted
13 Dec 2024
First published
14 Dec 2024

Green Chem., 2024, Accepted Manuscript

Advances of photocatalytic carboxylation of C(sp3)-H bond with CO2: A sustainable strategy for CO2 fixation

A. Das and A. J. David, Green Chem., 2024, Accepted Manuscript , DOI: 10.1039/D4GC04956J

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