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功能性多孔离子聚合物作为温和条件下CO化学固定的高效多相催化剂

Functional Porous Ionic Polymers as Efficient Heterogeneous Catalysts for the Chemical Fixation of CO under Mild Conditions.

作者信息

Dai Zhifeng, Long Yang, Liu Jianliang, Bao Yuanfei, Zheng Liping, Ma Jiacong, Liu Jiayi, Zhang Fei, Xiong Yubing, Lu Ji-Qing

机构信息

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.

出版信息

Polymers (Basel). 2022 Jun 29;14(13):2658. doi: 10.3390/polym14132658.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/466a/9269538/0c5e25f1cfd0/polymers-14-02658-sch001.jpg

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