Journal
MICROPOROUS AND MESOPOROUS MATERIALS
Volume 350, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.micromeso.2023.112447
Keywords
CO2; N-doped porous polymer; Ionic liquid; Cyclic carbonate
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A N-doped porous polymer with protonated ionic liquid sites was prepared by a solvent-free self-assembly synthesis and hydrobromic acid modification. The modified polymer, PIP-HP-HBr, maintained a high specific surface area and exhibited elevated catalytic activity with up to 99% yield of cyclic carbonates under metal/solvent/cocatalyst-free conditions. The PIP-HP-HBr catalyst also showed excellent cycling stability and could be easily recovered. The catalytic mechanism was proposed to be attributed to the synergistic effect of hydrogen bond donor -OH and nucleophilic anion Br-.
A N-doped porous polymer with protonated ionic liquid sites was fabricated by a solvent-free self-assembly synthesis of resorcinol/formaldehyde resin, followed by modification with hydrobromic acid (HBr) to introduce ionic sites. Compared with the parent polymer PIP-HP, polymer PIP-HP-HBr maintains a high specific surface area after ion site construction, and the elevated activity was also acquired under metal/solvent/cocatalyst-free conditions with up to 99% yield of cyclic carbonates. Furthermore, the PIP-HP-HBr as a heterogeneous catalyst can be readily recovered and demonstrate excellent cycling stability. In addition, a plausible catalytic mechanism had been proposed that the high catalytic activity originates from the synergistic effect of hydrogen bond donor -OH and nucleophilic anion Br-.
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