Nitrogen-rich covalent organic polymers and potassium iodide for efficient chemical fixation of CO2 into epoxides under mild conditions. Issue 11 (18th May 2021)

• Record Type: Journal Article
• Authors: Hao, Yongjing; Yan, Xiuli; Zhu, Zheng; Chang, Tao; Meng, Xiaocai; Fu, Xiying; Panchal, Balaji; Kang, Lianwei; Qin, Shenjun
• Is Part Of: Sustainable energy & fuels. Volume 5:Issue 11(2021)
• Page Start: 2943
• Page End: 2951
• Publication Date: 2021-05-18
• Subjects: Renewable energy sources -- Periodicals; Fuel cells -- Periodicals; Electric batteries -- Periodicals; Electrochemistry -- Periodicals; 660.297
• DOI: 10.1039/d1se00251a
• Languages: English
• ISSNs: 2398-4902

Abstract

Abstract : The synergistic interaction of KI and NUPs plays an important role in the fixation reaction of CO2 and epoxides. Abstract : Resource utilization of carbon dioxide (CO2 ) to add value to the chemicals used in the preparation of cyclic carbonates has gained significant interest in sustainable chemistry and environmental preservation. Herein, new nitrogen-rich urea covalent organic polymers (NUP-1, NUP-2, NUP-3 ) with multiple urea groups simultaneously acting as acidic nodes were designed and synthesized in a simple method. These synthesized NUPs were characterized using FT-IR spectroscopy, 13 C CP MAS NMR, SEM, PXRD, TGA, XPS spectroscopy, CO2 adsorption and nitrogen adsorption–desorption. The novel NUP-3 catalyst was particularly effective in the cycloaddition reactions having obtained a 93% yield of cyclic carbonate after 24 h at 90 °C with 0.1 MPa of pressure, using 1.0 mol% of KI and 70 mg of NUP-3 . The results showed that the functionalized NUP-3 used as a catalyst for the cycloaddition reaction of CO2 and epoxide with an alkali-metal salt, exhibited good activity under mild conditions. In addition, a mechanistic insight into the effects of urea groups on the activation of both epoxide and CO2 was gained using DFT calculations.