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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.

SUBMITTER: Shi D 

PROVIDER: S-EPMC5811127 | biostudies-other | 2015 Feb

REPOSITORIES: biostudies-other

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

Shi Dongying D   He Cheng C   Qi Bo B   Chen Cong C   Niu Jingyang J   Duan Chunying C  

Chemical science 20141030 2


The direct formation of new C-C bonds through photocatalytic oxidative coupling from low reactive sp<sup>3</sup> C-H bonds using environmentally benign and cheap oxygen as oxidant is an important area in sustainable chemistry. By incorporating the photoredox catalyst [SiW<sub>11</sub>O<sub>39</sub>Ru(H<sub>2</sub>O)]<sup>5-</sup> 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 Cu<sup>II<  ...[more]

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