Catalysis Conversion of Carbon Dioxide and Epoxides by Tetrahydroxydiboron To Prepare Cyclic Carbonates.
Yuhui LuoFei ChenHao ZhangJi-Chang LiuNing LiuPublished in: The Journal of organic chemistry (2023)
A binary catalytic system comprising tetrahydroxydiboron and tetrabutylammonium iodide (TBAI) was used to catalyze the cycloaddition of carbon dioxide (CO 2 ) with epoxides. The tetrahydroxydiboron catalyst (9 mol %), in combination with the use of TBAI (13.5 mol %) as a nucleophile, is capable of catalyzing the cycloaddition of CO 2 with various terminal epoxides under room temperature and a CO 2 balloon. In addition, a range of internal epoxides, including sterically hindered bicyclic epoxides and vegetable oil-based epoxides, were suitable for the catalytic system, affording a series of cyclic carbonates in moderate to high yields. The tetrahydroxydiboron/TBAI cooperative catalytic mechanism was elucidated using Fourier transform infrared spectroscopy, nuclear magnetic resonance, and electrospray ionization-high-resolution mass spectrometry. Results reveal that the tetrahydroxydiboron catalyst exhibits dual effects, activating both CO 2 and epoxides; initially, it underwent the insertion of CO 2 to form a boron-CO 2 adduct and subsequently activated the epoxides through interaction of the B-O bond.
Keyphrases
- carbon dioxide
- room temperature
- magnetic resonance
- ionic liquid
- high resolution mass spectrometry
- magnetic resonance imaging
- liquid chromatography
- gene expression
- dna methylation
- signaling pathway
- highly efficient
- high intensity
- fatty acid
- mass spectrometry
- metal organic framework
- high resolution
- ms ms
- gas chromatography
- ultra high performance liquid chromatography