TY - JOUR
T1 - Regulating the N-functional hydrogen bond donors over magnetic nanoparticles supported imidazole tribromide zinc ionic liquid for CO2 cycloaddition
AU - Chen, Jing
AU - Wu, Qin
AU - Shi, Daxin
AU - Chen, Kangcheng
AU - Zhang, Yaoyuan
AU - Liu, Helei
AU - Li, Hui
AU - Xu, Xiyan
AU - Li, Hansheng
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2025/1/5
Y1 - 2025/1/5
N2 - The design of catalysts for the mile production of cyclic carbonates by CO2 cycloaddition is of value. Magnetic polymer nanoparticles-supported imidazole tribromide zinc ionic liquid catalysts, incorporating N-functional hydrogen bond donors (HBD), was successfully accomplished. The correlation between the N-functional HBD and catalytic activity was thoroughly investigated through experimental studies and DFT calculations. The catalyst featuring a secondary amine group (NHM) demonstrated remarkable catalytic performance in CO2 cycloaddition reactions. Under optimized conditions, including 0.12 mol% catalyst dose, 100 °C, and nPO:nCO2 = 1:1.2 for 3 h, a complete conversion was achieved. The exceptional performance of the catalyst was attributed to the multicenter synergistic effect, arising from the appropriate electronegativity, minimal spatial site resistance, a balanced distance between the NHM and imidazolium ion, and the presence of multiple active centers (NHM, Zn2+, and Br−). The integration of a magnetic component enabled swift separation and exceptional recovery stability over 8 consecutive cycles.
AB - The design of catalysts for the mile production of cyclic carbonates by CO2 cycloaddition is of value. Magnetic polymer nanoparticles-supported imidazole tribromide zinc ionic liquid catalysts, incorporating N-functional hydrogen bond donors (HBD), was successfully accomplished. The correlation between the N-functional HBD and catalytic activity was thoroughly investigated through experimental studies and DFT calculations. The catalyst featuring a secondary amine group (NHM) demonstrated remarkable catalytic performance in CO2 cycloaddition reactions. Under optimized conditions, including 0.12 mol% catalyst dose, 100 °C, and nPO:nCO2 = 1:1.2 for 3 h, a complete conversion was achieved. The exceptional performance of the catalyst was attributed to the multicenter synergistic effect, arising from the appropriate electronegativity, minimal spatial site resistance, a balanced distance between the NHM and imidazolium ion, and the presence of multiple active centers (NHM, Zn2+, and Br−). The integration of a magnetic component enabled swift separation and exceptional recovery stability over 8 consecutive cycles.
KW - CO cycloaddition
KW - Density functional theory
KW - Hydrogen bond donors
KW - Intramolecular multicenter synergism
KW - Magnetic ionic liquid catalyst
UR - http://www.scopus.com/inward/record.url?scp=85204394173&partnerID=8YFLogxK
U2 - 10.1016/j.ces.2024.120731
DO - 10.1016/j.ces.2024.120731
M3 - Article
AN - SCOPUS:85204394173
SN - 0009-2509
VL - 301
JO - Chemical Engineering Science
JF - Chemical Engineering Science
M1 - 120731
ER -