Issue 23, 2024

Photocatalytic oxidative cyclization of aromatic thioamides catalyzed by Cu2O rhombic dodecahedra

Abstract

Cu2O rhombic dodecahedra were used to photocatalyze thiobenzamide cyclization in tetrahydrofuran (THF) forming 3,5-diphenyl-1,2,4-thiadiazole under 390 nm light illumination. The rhombic dodecahedra outperform cubic and octahedral Cu2O crystals. They can also photocatalyze thiobenzamides bearing a wide range of substituent groups with generally high product yields in 18 h at room temperature. Electron, hole and various radical scavenging experiments were performed to support the proposed reaction mechanism. This work demonstrates again that the use of surface-controlled metal oxide crystals offers huge cost advantages over the covalent organic framework (COF) photocatalysts for some organic transformations.

Graphical abstract: Photocatalytic oxidative cyclization of aromatic thioamides catalyzed by Cu2O rhombic dodecahedra

Supplementary files

Article information

Article type
Paper
Submitted
31 des. 2023
Accepted
05 feb. 2024
First published
07 feb. 2024
This article is Open Access
Creative Commons BY-NC license

J. Mater. Chem. A, 2024,12, 13792-13799

Photocatalytic oxidative cyclization of aromatic thioamides catalyzed by Cu2O rhombic dodecahedra

G. Wang and M. H. Huang, J. Mater. Chem. A, 2024, 12, 13792 DOI: 10.1039/D3TA08126E

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