Antonangelo Ariana R, Hawkins Natasha, Tocci Elena, Muzzi Chiara, Fuoco Alessio, Carta Mariolino
Department of Chemistry, Faculty of Science and Engineering, Swansea University, Grove Building, Singleton Park, Swansea SA2 8PP, U.K.
Institute on Membrane Technology, National Research Council of Italy (CNR-ITM), via P. Bucci 17/C, Rende (CS) 87036, Italy.
J Am Chem Soc. 2022 Aug 31;144(34):15581-15594. doi: 10.1021/jacs.2c04739. Epub 2022 Aug 16.
Heterogeneous catalysis plays a pivotal role in the preparation of value-added chemicals, and it works more efficiently when combined with porous materials and supports. Because of that, a detailed assessment of porosity and pore size is essential when evaluating the performance of new heterogeneous catalysts. Herein, we report the synthesis and characterization of a series of novel microporous Tröger's base polymers and copolymers (TB-PIMs) with tunable pore size. The basicity of TB sites is exploited to catalyze the Knoevenagel condensation of benzaldehydes and malononitrile, and the dimension of the pores can be systematically adjusted with an appropriate selection of monomers and comonomers. The tunability of the pore size provides the enhanced accessibility of the catalytic sites for substrates, which leads to a great improvement in conversions, with the best results achieving completion in only 20 min. In addition, it enables the use of large benzaldehydes, which is prevented when using polymers with very small pores, typical of conventional PIMs. The catalytic reaction is more efficient than the corresponding homogeneous counterpart and is ultimately optimized with the addition of a small amount of a solvent, which facilitates the swelling of the pores and leads to a further improvement in the performance and to a better carbon economy. Molecular dynamic modeling of the copolymers' structures is employed to describe the swellability of flexible chains, helping the understanding of the improved performance and demonstrating the great potential of these novel materials.
多相催化在增值化学品的制备中起着关键作用,当与多孔材料和载体结合时,其效率更高。因此,在评估新型多相催化剂的性能时,对孔隙率和孔径进行详细评估至关重要。在此,我们报告了一系列孔径可调的新型微孔特罗格碱聚合物和共聚物(TB-PIMs)的合成与表征。利用TB位点的碱性催化苯甲醛和丙二腈的Knoevenagel缩合反应,通过适当选择单体和共聚单体可以系统地调节孔的尺寸。孔径的可调性提高了催化位点对底物的可及性,从而使转化率大幅提高,最佳结果是仅在20分钟内就完成反应。此外,它还能使用大的苯甲醛,而使用传统PIMs典型的小孔径聚合物时则无法使用。该催化反应比相应的均相反应更有效,最终通过添加少量溶剂进行优化,这有助于孔的溶胀,从而进一步提高性能并实现更好的碳经济性。利用共聚物结构的分子动力学模型来描述柔性链的溶胀性,有助于理解性能的提高,并证明了这些新型材料的巨大潜力。