Microwave‐assisted fabrication of a mixed‐ligand [Cu4(μ3‐OH)2]‐cluster‐based metal–organic framework with coordinatively unsaturated metal sites for carboxylation of terminal alkynes with carbon dioxide. (13th May 2021)

• Record Type: Journal Article
• Authors: Wang, Wen‐Jing; Sun, Zhong‐Hua; Chen, Sheng‐Chun; Qian, Jun‐Feng; He, Ming‐Yang; Chen, Qun
• Is Part Of: Applied organometallic chemistry. Volume 35:Number 8(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-05-13
• Subjects: alkyne carboxylation -- carbon dioxide -- copper (II)‐based MOF -- microwave synthesis; Organometallic chemistry -- Periodicals; Organometallic compounds -- Periodicals; 547.05
• DOI: 10.1002/aoc.6288
• Languages: English
• ISSNs: 0268-2605

Abstract

Abstract : The development of efficient and stable metal–organic framework (MOF) catalysts with coordinatively unsaturated metal sites for modern organic synthesis is greatly important. Herein, a robust [Cu4 (μ3 ‐OH)2 ]‐cluster‐based MOF (Cu‐MOF) with a mixed‐ligand system was successfully fabricated by a microwave‐assisted method under mild conditions. The as‐prepared Cu‐MOF catalyst possessing unsaturated Cu (II) sites exhibited excellent catalytic activity toward the direct carboxylation of 1‐ethynylbenzene with CO2, and various propiolic acid derivatives were synthesized in moderate to good yields under optimized reaction conditions. Furthermore, the catalyst remained stable and could be easily recycled for five sequential runs without incredible decrease in catalytic efficiency. Abstract : A robust [Cu4 (μ3 ‐OH)2 ]‐cluster‐based metal–organic framework (Cu‐MOF) based on tetranuclear [Cu4 (μ3 ‐OH)2 ] units was synthesized through a microwave‐assisted, facile and fast method and was applied to catalyze the direct carboxylation of terminal alkynes with CO2 . The exceptional functional group tolerance was also found combining with remarkable stability and reusability.