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

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(sp...

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Published inGreen chemistry : an international journal and green chemistry resource : GC Vol. 23; no. 18; pp. 6984 - 6989
Main Authors Jin, Yunhe, Zhang, Qingqing, Wang, Lifang, Wang, Xinyao, Meng, Changgong, Duan, Chunying
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 21.09.2021
Royal Society of Chemistry
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Summary: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(sp 3 )-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. A practical and green iron-catalyzed photoredox system for C-H functionalization of ethane, propane, and other light alkanes was developed.
Bibliography:H
10.1039/d1gc01563j
1
C NMR spectra of these synthesised compounds. See DOI
Electronic supplementary information (ESI) available: Mechanism investigations, synthetic procedures, characterisation data and
13
ISSN:1463-9262
1463-9270
DOI:10.1039/d1gc01563j