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Food safety is a great concern of the general public. Chlorophenols (CPs) as organic pollutant can be found in drinking water and foods, causing serious harm to human health. Herein, imine-linked covalent organic frameworks (COFs), named as TAPT-AN-COF, was synthesized by aniline modulation strategy through condensation of 1,3,5-triformylphoroglucinol and 4,4',4''-(1,3,5-Triazine-2,4,6-triyl)trianiline with aniline as modulator. The prepared TAPT-AN-COF possesses good crystallinity and regular morphology, displaying excellent adsorption capability towards CPs pollutants. Thus, the TAPT-AN-COF was used as novel adsorbent for off-line solid-phase extraction of four CPs (2-CP, 3-CP, 2,3-CPs, 2,4-CPs) from bottled water, tea drink and honey samples before high performance liquid chromatography-ultraviolet detection. Under optimal conditions, wide linear range, low detection limits and satisfactory extraction recovery were gained. The π-stacking and hydrophobic interactions between the TAPT-AN-COF and the analytes played an important role in the adsorption. The established method has a great potential in determining other hydrophobic aromatic compounds.
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http://dx.doi.org/10.1016/j.chroma.2021.462610 | DOI Listing |
Anal Chem
September 2025
Research Center for Analytical Sciences, Department of Chemistry, College of Sciences, Northeastern University, Shenyang 110819, China.
Covalent organic frameworks (COFs) exhibit exceptional adsorption capacity but suffer from challenging desorption. In this study, a bromine-functionalized magnetic COF composite (FeO@COF-Br) was synthesized via bromodimethylsulfonium bromide-mediated bromination of imine-linked COF on FeO nanospheres (FeO@COF), where the COF framework was constructed by 1,3,5-tris(4-formylphenyl)benzene and 2,6-diamino-3,5-diethynylpyridine. Compared with pristine FeO@COF, FeO@COF-Br enhanced desorption efficiencies for brominated contaminants by about 30% while maintaining adsorption capacity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
School of Chemistry and Chemical Engineering, Anhui University of Technology, Ma'anshan, 243000, China.
The photocatalytic efficiency of two-dimensional covalent organic frameworks (2D COFs) is governed by the spatial arrangement of donor-acceptor (D-A) moieties, which strongly influences exciton transport. However, precise control over D-A alignment, especially across intra- and interlayer dimensions, remains a key challenge for optimizing singlet oxygen (O) generation. Here, we present a linker geometry-directed approach to modulate D-A organization within perylene diimide (PDI)-based COFs.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, The University of Hong Kong, Hong Kong 999077, China.
While intricate designs have been implemented to transform noble-metal complexes and sophisticated organic molecules into reactive photocatalysts for the single-electron reduction of unactivated alkyl halides, the development of highly reducing photocatalytic systems based on earth-abundant metals is still in its early stages. Herein, we show that a simple terpyridine-ligated nickel(II) complex, integrated into an imine-linked covalent organic framework, can be readily reduced by photoexcited Hantzsch esters to produce a heterogeneous nickel(I) photocatalyst with a fairly low excited-state oxidation potential of approximately -3.5 V (referenced to the saturated calomel electrode).
View Article and Find Full Text PDFJ Hazard Mater
August 2025
College of Chemistry and Materials Engineering, Zhejiang A&F University, Hangzhou 311300, China. Electronic address:
Imine-linked covalent organic frameworks (COFs) are considered as promising adsorbents to remove the water contaminants. However, the reversibility and hydrolyzation of imine bond may generate limited stability in long-term aqueous environment-based applications, and the improved stability of imine-linked COFs is highly desired. In this work, a carboxyl-quinoline linked COFs (CQ-COF) was synthesized by the cyclization of imine linkage via one-step modification.
View Article and Find Full Text PDFSmall
August 2025
Chemistry Program, New York University Abu Dhabi, Saadiyat Island, 129188, UAE.
Controlling the crystallinity and porosity of 2D covalent organic frameworks (2D COFs) is crucial for their applications in science and technology. Herein, the construction of 2D COFs, COF-TP-X, is reported using a multicomponent reaction strategy that introduces β-ketoenamine linkages into isostructural imine-linked COFs. This approach yields materials with exceptional crystallinity, stability, and tunable hydrophilicity.
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