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利用烷基胺作为构筑块制备腙键连接的共价有机框架,用于高吸附金属离子。

Fabrication of Hydrazone-Linked Covalent Organic Frameworks Using Alkyl Amine as Building Block for High Adsorption Capacity of Metal Ions.

机构信息

CAS Key Laboratory of Separation Science for Analytical Chemistry , Dalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023 , China.

Key Laboratory of Synthetic and Natural Function Molecule Chemistry of Ministry of Education, College of Chemistry and Materials Science , Northwest University , Xi'an 710069 , China.

出版信息

ACS Appl Mater Interfaces. 2019 Mar 27;11(12):11706-11714. doi: 10.1021/acsami.8b18502. Epub 2019 Mar 18.

Abstract

There are several researches on the preparation and application of hydrazone-linked covalent organic frameworks (COFs), and all of them generally necessitate rigid aromatic amines. Herein, we report a strategy for design and synthesis of COF with flexible alkyl amine as a building block and intramolecular hydrogen bonding as a knot in the network. The proof-of-concept design was demonstrated by exploring 1,3,5-triformylphloroglucinol and oxalyldihydrazide (ODH) as precursors to synthesize a novel COF material (TpODH), in which different organic building units are combined through hydrazone bonds to form two-dimensional porous frameworks. It should be pointed that irreversible enol-to-keto tautomerism and intramolecular N-H···O═C hydrogen bonding of TpODH would enhance the crystallinity and chemical stability, leading to large specific surface area of 835 m g. However, another COF synthesized with 1,3,5-triformylbenzene and ODH exhibited less crystallinity and low special surface area (94 m g). Representatively, the resulting TpODH afforded Cu(II) and Hg(II) capacities of 324 and 1692 mg g, respectively, which exceeded that of most COFs previously reported. Moreover, the Fourier-transform infrared and X-ray photoelectron spectroscopy spectra analyses were taken to demonstrate the adsorption mechanism. These results suggested that the materials could be applied to the removal of metallic ions in the future.

摘要

有几项关于腙键合共价有机框架(COFs)的制备和应用的研究,它们都通常需要刚性的芳香胺。在此,我们报告了一种以柔性烷基胺为构建块、分子内氢键为网络节点设计和合成 COF 的策略。通过探索均苯三甲醛和草酰二肼(ODH)作为前体制备了一种新型 COF 材料(TpODH),证明了这一概念设计,其中不同的有机构建单元通过腙键结合形成二维多孔框架。值得指出的是,TpODH 的不可逆烯醇-酮互变异构和分子内 N-H···O=C 氢键会增强其结晶度和化学稳定性,从而导致其具有 835 m g 的大比表面积。然而,用 1,3,5-均苯三甲酰氯和 ODH 合成的另一种 COF 的结晶度较低,比表面积较小(94 m g)。代表性地,所得的 TpODH 对 Cu(II)和 Hg(II)的容量分别为 324 和 1692 mg g,超过了大多数先前报道的 COFs。此外,傅里叶变换红外和 X 射线光电子能谱分析表明了吸附机理。这些结果表明,该材料未来可用于去除金属离子。

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