Issue 18, 2019

Small-molecule activation with iron porphyrins using electrons, photons and protons: some recent advances and future strategies

Abstract

Substituted tetraphenyl Fe porphyrins are versatile molecular catalysts for the activation of small molecules (such as O2, H+ or CO2), which could lead to renewable energy storage, the direct production of fuels or new catalytic relevant processes. Herein, we review the recent studies of these earth-abundant metal catalysts for the electrochemical activation of dioxygen on the one hand and for the photostimulated reduction of carbon dioxide on the other hand. These two prototype reactions illustrate how mechanistic studies are the only rational approach to gain fundamental insights into the elementary steps that drive the catalysis and for identification of the key intrinsic parameters controlling the reactivity, offering in turn the possibility to rationally tune the structure of the catalysts as well as the catalytic conditions.

Graphical abstract: Small-molecule activation with iron porphyrins using electrons, photons and protons: some recent advances and future strategies

Article information

Article type
Perspective
Submitted
10 Janv. 2019
Accepted
22 Febr. 2019
First published
22 Febr. 2019

Dalton Trans., 2019,48, 5869-5878

Small-molecule activation with iron porphyrins using electrons, photons and protons: some recent advances and future strategies

E. Anxolabéhère-Mallart, J. Bonin, C. Fave and M. Robert, Dalton Trans., 2019, 48, 5869 DOI: 10.1039/C9DT00136K

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