Tröger’s Base Network Polymers of Intrinsic Microporosity (TB-PIMs) with Tunable Pore Size for Heterogeneous Catalysis

微型多孔材料 化学 催化作用 聚合物 多相催化 共聚物 化学工程 多孔性 Knoevenagel冷凝 单体 丙二腈 同种类的 溶剂 高分子化学 有机化学 工程类 物理 热力学
作者
Ariana R. Antonangelo,Natasha Hawkins,Elena Tocci,Chiara Muzzi,Alessio Fuoco,Mariolino Carta
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:144 (34): 15581-15594 被引量:27
标识
DOI:10.1021/jacs.2c04739
摘要

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.
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