构建基于的离子共价有机框架,用于吸附阳离子染料的位
Tingting Huang1, Ke Li1, Xiaoqin Shen1
1School of Chemical Science and Engineering, Tongji University, Siping Road 1239, Shanghai 200092, China.
ACS applied materials & interfaces
|December 1, 2025
概括
研究人员使用合成后的修改来增强染料吸附,创建了阴离子共价有机框架 (COF). 这些阴离子COF显著改善了从水中去除阳离子染料的过程.
科学领域:
- 材料科学 材料科学 材料科学
- 化学 化学 化学
- 环境科学 环境科学
背景情况:
- 由于单体的限制,直接合成阴离子共价有机框架 (COF) 是一个挑战.
- 合成后修饰 (PSM) 是一种可行的策略,可以在COF中引入阴离子位点.
研究的目的:
- 通过PSM通过不同的位合成有氧化碳化合物.
- 为了研究这些阴离子COF对阳离子染料的吸附性质.
- 为了阐明增强染料吸附背后的机制.
主要方法:
- BIPY-COF的合成及其随后的修改为HI/BIPY-COF和CH3I/BIPY-COF.
- 使用酸10 (AO),甲基 (MO) 和乙二 (ED) 的吸附性研究.
- 理论计算和仪器表征,以了解吸附机制.
主要成果:
- 与原始COF相比,阴离子COF对阴离子染料具有显著增强的吸附能力.
- 甲基的吸附能力从12.2 mg/g增加到122.7 mg/g和174.3 mg/g.
- 电静电相互作用被确定为吸附过程中的关键因素.
结论:
- 含有的COF的合成后改性是一种有效的途径,可以制造阴阳性材料.
- 阴离子COF具有很大的潜力,可以有效地从水溶液中去除阳离子染料.
- 这项研究为设计用于环境修复的先进COF提供了宝贵的参考.
相关概念视频
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
3.6K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
3.6K
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
3.8K
Nitrous acid and nitric acids are two types of acids containing nitrogen, among which nitrous acid is weaker than nitric acid. Nitrous acid with a pKa value of 3.37 ionizes in water to give a nitrite ion and the hydronium ion.
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
3.8K
Ion Exchange
1.1K
Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
1.1K
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
4.7K
Nitrous acid is a relatively weak and unstable acid prepared in situ by the reaction of sodium nitrite and cold, dilute hydrochloric acid. In an acidic solution, the nitrous acid undergoes protonation when it loses water to form a nitrosonium ion—an electrophile. Nitrous acid reacts with primary amines to give diazonium salts. The reaction is called diazotization of primary amines.
4.7K
Anionic Chain-Growth Polymerization: Overview
2.5K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.5K
Metal-Ligand Bonds
23.9K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
23.9K


