杂原子
共价有机骨架
催化作用
吸附
共价键
化学工程
间苯二酚
炔丙基
聚合物
纳米复合材料
化学
材料科学
纳米颗粒
高分子化学
有机化学
纳米技术
工程类
戒指(化学)
作者
Debanjan Chakraborty,Pragalbh Shekhar,Himan Dev Singh,Rinku Kushwaha,C. P. Vinod,Ramanathan Vaidhyanathan
标识
DOI:10.1002/asia.201901157
摘要
Covalent organic frameworks are a new class of crystalline organic polymers possessing a high surface area and ordered pores. Judicious selection of building blocks leads to strategic heteroatom inclusion into the COF structure. Owing to their high surface area, exceptional stability and molecular tunability, COFs are adopted for various potential applications. The heteroatoms lining in the pores of COF favor synergistic host-guest interaction to enhance a targeted property. In this report, we have synthesized a resorcinol-phenylenediamine-based COF which selectively adsorbs CO2 into its micropores (12 Å). The heat of adsorption value (32 kJ mol-1 ) obtained from the virial model at zero-loading of CO2 indicates its favorable interaction with the framework. Furthermore, we have anchored small-sized Ag nanoparticles (≈4-5 nm) on the COF and used the composite for chemical fixation of CO2 to alkylidene cyclic carbonates by reacting with propargyl alcohols under ambient conditions. Ag@COF catalyzes the reaction selectively with an excellent yield of 90 %. Recyclability of the catalyst has been demonstrated up to five consecutive cycles. The post-catalysis characterizations reveal the integrity of the catalyst even after five reaction cycles. This study emphasizes the ability of COF for simultaneous adsorption and chemical fixation of CO2 into corresponding cyclic carbonates.
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