Issue 2, 2015

Merging of the photocatalysis and copper catalysis in metal–organic frameworks for oxidative C–C bond formation

Abstract

The direct formation of new C–C bonds through photocatalytic oxidative coupling from low reactive sp3 C–H bonds using environmentally benign and cheap oxygen as oxidant is an important area in sustainable chemistry. By incorporating the photoredox catalyst [SiW11O39Ru(H2O)]5− into the pores of Cu-based metal–organic frameworks, a new approach for merging Cu-catalysis/Ru-photocatalysis within one single MOF was achieved. The direct CuII–O–W(Ru) bridges made the two metal catalyses being synergetic, enabling the application on the catalysis of the oxidative coupling C–C bond formation from acetophenones and N-phenyl-tetrahydroisoquinoline with excellent conversion and size-selectivity. The method takes advantage of visible light photoredox catalysis to generate iminium ion intermediate from N-phenyl-tetrahydroisoquinoline under mild conditions and the easy combination with Cu-catalyzed activation of nucleophiles. Control catalytic experiments using similar Cu-based sheets but with the photoredox catalytic anions embedded was also investigated for comparison.

Graphical abstract: Merging of the photocatalysis and copper catalysis in metal–organic frameworks for oxidative C–C bond formation

Supplementary files

Article information

Article type
Edge Article
Submitted
05 Aug 2014
Accepted
27 Oct 2014
First published
30 Oct 2014
This article is Open Access

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

Chem. Sci., 2015,6, 1035-1042

Author version available

Merging of the photocatalysis and copper catalysis in metal–organic frameworks for oxidative C–C bond formation

D. Shi, C. He, B. Qi, C. Chen, J. Niu and C. Duan, Chem. Sci., 2015, 6, 1035 DOI: 10.1039/C4SC02362E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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