Issue 11, 2024

Carboxylation reactions for the sustainable manufacture of chemicals and monomers

Abstract

Carboxylation stands out as one of the most versatile and viable routes for carbon dioxide fixation, a crucial chemical transformation essential for advancing capture technologies and fostering a sustainable industry. The carboxylic acids and derivatives produced through this process hold considerable interest for various sectors, including pharmaceuticals and polymers. Presently, most of these chemicals are derived from non-renewable resources, underscoring the imperative need to develop sustainable pathways for their synthesis. The inherent stability of the CO2 molecule, owing to its high oxidation state and linear configuration, poses significant challenges for activation. Diverse approaches, including photochemical, electrochemical, enzymatic, and thermochemical carboxylation have been explored. While noteworthy results have been achieved with these methods, substantial efforts are still required to facilitate their scalability. This review provides a comprehensive overview of each of these routes, elucidating their respective strengths and weaknesses. Emphasis is placed on thermochemical routes, given their proximity to potential industrial-scale application.

Graphical abstract: Carboxylation reactions for the sustainable manufacture of chemicals and monomers

Article information

Article type
Critical Review
Submitted
14 Aug. 2024
Accepted
29 Sept. 2024
First published
30 Sept. 2024
This article is Open Access
Creative Commons BY-NC license

RSC Sustain., 2024,2, 3167-3182

Carboxylation reactions for the sustainable manufacture of chemicals and monomers

L. Faba and S. Ordóñez, RSC Sustain., 2024, 2, 3167 DOI: 10.1039/D4SU00482E

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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