Relay catalysis of hydrocarbon oxidation using O2 in the confining domain of 3D metalloporphyrin-based metal-organic frameworks with bimetallic catalytic centers. (12th October 2022)

• Record Type: Journal Article
• Authors: Shen, Hai-Min; Guo, A-Bing; Zhang, Yu; Liu, Qiu-Ping; Qin, Jia-Wei; She, Yuan-Bin
• Is Part Of: Chemical engineering science. Volume 260(2022)
• Publication Date: 2022-10-12
• Subjects: Partial oxidation -- Hydrocarbon -- Relay catalysis -- MOFs -- Metalloporphyrins; Chemical engineering -- Periodicals; Génie chimique -- Périodiques; Chemical engineering; Periodicals; Electronic journals; 660
• DOI: 10.1016/j.ces.2022.117825
• Languages: English
• ISSNs: 0009-2509

Abstract

Graphical abstract: Conversion and selectivity to partial oxidation products in oxidation of hydrocarbons with O2 were increased simultaneously through relay catalysis in confining domains of PCN-224(Co&Ni) possessing bimetallic catalytic centers. Highlights: A novel and effective relay catalysis mode in confining domains was presented. Relay catalysis in confining domains favored selective CH bonds oxidation with O2 . Disordered free radical diffusion was suppressed by confining catalytic domains. Oxidation intermediate R-OOH was used as additional oxidant to oxidize substrate. Simultaneously increased conversion and selectivity in CH bonds oxidation with O2 . Abstract: To realize efficient and selective oxidation of hydrocarbons with O2, 3D MOFs possessing bimetallic centers were prepared to construct confining domains and relay catalysis sites. Applied to oxidation of hydrocarbons, optimum performance was observed in PCN-224(Co&Ni) as catalyst. Both of conversion and selectivity towards partial oxidation products were enhanced. In the significant cyclohexane oxidation, conversion increased from 5.89% to 7.26% with selectivity rose from 81.5% to 85.2%. Superior performance of PCN-224(Co&Ni) was attributed to suppressed free radical diffusion in confining domains of PCN-224(Co&Ni), enhanced oxidation of C-H bonds with oxidation intermediate R-OOH in relay catalysis, and decreased contact between partial oxidation products and catalytic centers. The relay catalysis mode and catalytic mechanism were also studied. The relay catalysis in confining domains herein provided a novel and effective strategy for selective and efficient oxidative functionalization of hydrocarbons, but also an intelligent and valuable idea for other chemical transformations involved free radicals.