Issue 9, 2025

Auto-relay catalysis for the oxidative carboxylation of alkenes into cyclic carbonates by a MOF catalyst

Abstract

In this study, we present the preparation and application of a new manganoporphyrin Hf-MOF catalyst, Hf-PCN-222(Mn) for the direct oxidative carboxylation of alkenes with CO2, leading to the effective formation of cyclic organic carbonates (COCs). In contrast to the conventional two-step process, this one-step methodology eliminates the need for the preparation, purification, and handling of epoxides. Hf-PCN-222(Mn) operates under very mild conditions, enabling the synthesis of a wide variety of COCs from alkenes (23 examples, up to 75% yield), as well as the chemoselective and size-selective carboxylation of dienes (7 examples, up to 61% yield). Additionally, we observed that Hf-PCN-222(Mn) could be recycled multiple times without significant loss of activity, providing insight into the sustainability of this approach.

Graphical abstract: Auto-relay catalysis for the oxidative carboxylation of alkenes into cyclic carbonates by a MOF catalyst

Supplementary files

Article information

Article type
Paper
Submitted
16 dec 2024
Accepted
27 jan 2025
First published
30 jan 2025
This article is Open Access
Creative Commons BY license

Green Chem., 2025,27, 2439-2448

Auto-relay catalysis for the oxidative carboxylation of alkenes into cyclic carbonates by a MOF catalyst

H. Phan, P. de la Cruz-Sánchez, M. J. Cabrera-Afonso and B. Martín-Matute, Green Chem., 2025, 27, 2439 DOI: 10.1039/D4GC06360K

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