Issue 18, 2021

Convenient C(sp3)–H bond functionalisation of light alkanes and other compounds by iron photocatalysis

Abstract

Light alkanes are natural organic carbon sources and widely distributed in nature. Transforming them into value-added fine chemicals affords attractively economic and ecological benefits as well as enormous chemical challenges. Herein, we report a practical iron-catalysed photoredox system for C(sp3)–H transformation of ethane, propane, and other light alkanes to C–N and C–C bonds under ambient temperature. The present method with abundant and inexpensive iron salts as photocatalysts exhibits high catalytic efficiency (turnover number up to 8000), mild conditions, and the convenience of being purified and scaled up without chromatography. A photo-induced ligand-to-metal charge transfer between Fe(III) and Cl generates a highly active chlorine radical that sequentially acts as hydrogen atom transfer catalyst. Therefore, the sustainable, convenient, and environmentally friendly system will find wide applications in high-value-added transformation of natural alkanes with novel inspiration not only for organic synthesis, but also for designing catalytically active organic/inorganic materials.

Graphical abstract: Convenient C(sp3)–H bond functionalisation of light alkanes and other compounds by iron photocatalysis

Supplementary files

Article information

Article type
Paper
Submitted
05 5 2021
Accepted
08 7 2021
First published
09 7 2021

Green Chem., 2021,23, 6984-6989

Convenient C(sp3)–H bond functionalisation of light alkanes and other compounds by iron photocatalysis

Y. Jin, Q. Zhang, L. Wang, X. Wang, C. Meng and C. Duan, Green Chem., 2021, 23, 6984 DOI: 10.1039/D1GC01563J

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