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Urea-Based Porous Organic Frameworks: Effective Supports for Catalysis in Neat Water

机译:尿素基多孔有机框架:净化水中的有效支持

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摘要

Two urea-based porous organic frameworks, UOF- 1 and UOF-2, were synthesized through a urea-forming condensation of 1,3,5-benzenetriisocyanate with 1,4-diaminobenzene and benzidine, respectively. UOF-1 and UOF-2 possess good hydrophilic properties and high scavenging ability for palladium. Their palladium polymers, Pd~(II)/UOF-1 and Pd~(II)/ UOF-2, exhibit high catalytic activity and selectivity for Suzuki–Miyaura cross-coupling reactions and selective reduction of nitroarenes in water. The catalytic reactions can be efficiently performed at room temperature. Palladium nanoparticles with narrow size distribution were formed after the catalytic reaction and were well dispersed in UOF-1 and UOF-2. XPS analysis confirmed the coordination of the urea oxygen atom with palladium. SEM and TEM images showed that the original network morphology of UOF-1 and UOF-2 was maintained after palladium loading and catalytic reactions.
机译:通过分别将1,3,5-苯三异氰酸酯与1,4-二氨基苯和联苯胺形成脲的缩合反应,合成了两种基于尿素的多孔有机骨架UOF-1和UOF-2。 UOF-1和UOF-2具有良好的亲水性和对钯的高清除能力。他们的钯聚合物Pd〜(II)/ UOF-1和Pd〜(II)/ UOF-2对铃木-宫浦交叉偶联反应和水中硝基芳烃的选择性还原具有很高的催化活性和选择性。催化反应可以在室温下有效地进行。催化反应后,形成了具有窄尺寸分布的钯纳米粒子,并很好地分散在UOF-1和UOF-2中。 XPS分析证实了脲氧原子与钯的配位。 SEM和TEM图像表明,钯负载和催化反应后,UOF-1和UOF-2的原始网络形态得以保留。

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