Dai Zhifeng, Long Yang, Liu Jianliang, Bao Yuanfei, Zheng Liping, Ma Jiacong, Liu Jiayi, Zhang Fei, Xiong Yubing, Lu Ji-Qing
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China.
Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province, Department of Chemistry, College of Science, Zhejiang Sci-Tech University, Hangzhou 310018, China.
Polymers (Basel). 2022 Jun 29;14(13):2658. doi: 10.3390/polym14132658.
The development of efficient and metal-free heterogeneous catalysts for the chemical fixation of CO into value-added products is still a challenge. Herein, we reported two kinds of polar group (-COOH, -OH)-functionalized porous ionic polymers (PIPs) that were constructed from the corresponding phosphonium salt monomers (v-PBC and v-PBH) using a solvothermal radical polymerization method. The resulting PIPs (POP-PBC and POP-PBH) can be used as efficient bifunctional heterogeneous catalysts in the cycloaddition reaction of CO with epoxides under relatively low temperature, ambient pressure, and metal-free conditions without any additives. It was found that the catalytic activities of the POP-PBC and POP-PBH were comparable with the homogeneous catalysts of Me-PBC and PBH and were higher than that of the POP-PPh-COOH that was synthesized through a post-modification method, indicating the importance of the high concentration catalytic active sites in the heterogeneous catalysts. Reaction under low CO concentration conditions showed that the activity of the POP-PBC (with a conversion of 53.8% and a selectivity of 99.0%) was higher than that of the POP-PBH (with a conversion of 32.3% and a selectivity of 99.0%), verifying the promoting effect of the polar group (-COOH group) in the porous framework. The POP-PBC can also be recycled at least five times without a significant loss of catalytic activity, indicating the high stability and robustness of the PIPs-based heterogeneous catalysts.
开发用于将CO化学固定为增值产品的高效无金属多相催化剂仍然是一项挑战。在此,我们报道了两种由相应的鏻盐单体(v-PBC和v-PBH)通过溶剂热自由基聚合法构建的极性基团(-COOH,-OH)功能化的多孔离子聚合物(PIPs)。所得的PIPs(POP-PBC和POP-PBH)可在相对低温、常压和无金属条件下,无需任何添加剂,用作CO与环氧化物环加成反应中的高效双功能多相催化剂。发现POP-PBC和POP-PBH的催化活性与Me-PBC和PBH的均相催化剂相当,且高于通过后修饰法合成的POP-PPh-COOH,这表明多相催化剂中高浓度催化活性位点的重要性。在低CO浓度条件下的反应表明,POP-PBC(转化率为53.8%,选择性为99.0%)的活性高于POP-PBH(转化率为32.3%,选择性为99.0%),证实了多孔骨架中极性基团(-COOH基团)的促进作用。POP-PBC还可循环至少五次而催化活性无显著损失,表明基于PIPs的多相催化剂具有高稳定性和稳健性。