Regulating the N-functional hydrogen bond donors over magnetic nanoparticles supported imidazole tribromide zinc ionic liquid for CO2 cycloaddition

Jing Chen, Qin Wu*, Daxin Shi, Kangcheng Chen, Yaoyuan Zhang, Helei Liu, Hui Li, Xiyan Xu, Hansheng Li

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Article number120731
JournalChemical Engineering Science
Volume301
DOIs
Publication statusPublished - 5 Jan 2025

Keywords

  • CO cycloaddition
  • Density functional theory
  • Hydrogen bond donors
  • Intramolecular multicenter synergism
  • Magnetic ionic liquid catalyst

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