Issue 40, 2025

Chiral heterogeneous photocatalysts for enantioselective synthesis: standing on the shoulders of organocatalysis

Abstract

Crafting organic molecules with control over their absolute stereochemistry is a challenging task for synthetic chemists. The present Perspective encompasses recent examples of enantioselective transformations based on chiral heterogeneous photocatalysts, including metal–organic frameworks (MOFs), covalent organic frameworks (COFs) and hybrid metal-halide perovskites (MHPs). Such materials combine a photocatalytic unit and a chiral element in a single component: the former is responsible for substrate activation, while the latter, typically a small organic molecule – i.e., an organocatalyst –, takes care of stereoinduction instead. Although synthetic applications are still limited to a handful of (benchmark) C–C and C–N bond formations and oxidation protocols, their number is expected to grow steadily in the near future. This trend is supported by cross-disciplinary knowledge transfer from the field of asymmetric organocatalysis, which is also driving the application of these materials in broader areas, such as solar-to-chemical energy conversion and chiral sensing technologies.

Graphical abstract: Chiral heterogeneous photocatalysts for enantioselective synthesis: standing on the shoulders of organocatalysis

Article information

Article type
Perspective
Submitted
11 Sep 2025
Accepted
24 Sep 2025
First published
30 Sep 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2025,16, 18496-18503

Chiral heterogeneous photocatalysts for enantioselective synthesis: standing on the shoulders of organocatalysis

C. Callegari, M. Moroni, D. Ravelli and L. Malavasi, Chem. Sci., 2025, 16, 18496 DOI: 10.1039/D5SC07001E

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