Physical/Materials Chemistry Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
Academy of Scientific and Innovative Research (AcSIR) , New Delhi-110020, India.
ACS Appl Mater Interfaces. 2017 Apr 19;9(15):13785-13792. doi: 10.1021/acsami.7b02355. Epub 2017 Apr 10.
The development of nanoparticle-polymer-hybrid-based heterogeneous catalysts with high reactivity and good recyclability is highly desired for their applications in the chemical and pharmaceutical industries. Herein, we have developed a novel synthetic strategy by choosing a predesigned metal-anchored building block for in situ generation of metal (Pd) nanoparticles in the stable, porous, and crystalline covalent organic framework (COF), without using conventional reducing agents. In situ generation of Pd nanoparticles in the COF skeleton is explicitly confirmed from PXRD, XPS, TEM images, and N NMR spectral analysis. This hybrid material is found to be an excellent reusable heterogeneous catalyst for the synthesis of biologically and pharmaceutically important 2-substituted benzofurans from 2-bromophenols and terminal alkynes via a tandem process with the turnover number up to 1101. The heterogeneity of the catalytic process is unambiguously verified by a mercury poisoning experiment and leaching test. This hybrid material shows superior catalytic performance compared to commercially available homogeneous as well as heterogeneous Pd catalysts.
开发具有高反应性和良好可回收性的基于纳米粒子-聚合物-杂化的多相催化剂对于它们在化学和制药工业中的应用是非常需要的。在此,我们选择了一种预设计的金属锚定结构单元,通过原位生成金属(Pd)纳米粒子的方法,在稳定、多孔和结晶的共价有机骨架(COF)中合成了一种新型的合成策略,而无需使用传统的还原剂。从 PXRD、XPS、TEM 图像和 N NMR 光谱分析明确证实了 COF 骨架中 Pd 纳米粒子的原位生成。该杂化材料被发现是一种非常优秀的可重复使用的多相催化剂,可通过串联过程从 2-溴苯酚和末端炔烃合成具有生物和药物重要性的 2-取代苯并呋喃,其周转数高达 1101。通过汞中毒实验和浸出实验明确验证了催化过程的多相性。与商业上可用的均相和多相 Pd 催化剂相比,该杂化材料表现出优异的催化性能。