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In this work, a three-dimensional metal-organic framework, [CdL(HO)] (Cd-MOF) was synthesized by using 2-(6-carboxypyridin-2-yl)terephthalic acid ligand (HL); and its post-synthetic modification composite, Eu@Cd-MOF was obtained by one-pot reaction of Euions with Cd-MOF. The FT-IR, PXRD, XPS, EDS, and fluorescence spectra were employed to verify the successful encapsulation of Euions into Cd-MOF. The luminescence measurements showed that Eu@Cd-MOF had a fluorescence quenching response with minocycline (MC), a widely used drug of broad-spectrum tetracycline antibiotics; and its limit of detection (LOD) for MC was 6.94 × 10 M. It was worth pointing out that Eu@Cd-MOF had the characteristics of high selectivity, excellent selectivity, fast response time, and considerable recyclability in the identification of MC. The quenching mechanism of Eu@Cd-MOF by MC was investigated by the FT-IR, PXRD, UV-vis, and theoretical calculations of Materials Studio (MS). The above results indicated that the fluorescence quenching of Eu@Cd-MOF was caused by the acceptor photo-induced electron transfer process (a-PET) and the UV competition absorption. In addition, a hydrogel membrane based on Eu@Cd-MOF was also fabricated, which can be used to visually inspect MC with the naked eyes in practical applications.
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http://dx.doi.org/10.1016/j.saa.2025.126867 | DOI Listing |
Chemphyschem
September 2025
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
Excessive fossil fuel combustion has accelerated renewable energy development, with hydrogen energy emerging as a promising alternative due to its high energy density and environmental compatibility. Photocatalytic hydrogen production through solar energy conversion represents a viable approach for sustainable development. Metal-organic frameworks (MOFs) have garnered significant research interest owing to their structural tunability, well-defined catalytic sites, and post-synthetic modification capabilities.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Chemistry, Zhejiang University, 866 Yuhangtang Road, Hangzhou, 310058, P.R. China.
Porous organic cages (POCs) have emerged as promising porous materials for a wide range of applications. However, their development is often limited by insufficient chemical stability and challenges in systematically functionalization. Herein, we reported the design and synthesis of a tetrazine-based POC (TC1) featuring rigid tetrahedral structure, prepared via a one-pot nucleophilic aromatic substitution reaction.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Laboratory of Solar Fuel, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, PR China; Chemistry Department, Faculty of Science, Fayoum University, Fayoum 63514, Egypt. Electronic address:
Post-synthetic modification (PSM) offers a promising approach for tailoring the compositional, structural, and electronic properties of covalent organic frameworks (COFs), thereby enhancing their exciton dissociation ability and facilitating charge transfer. The effectiveness of these approaches is largely compromised by the harsh conditions, complexity, and alteration of the original structure. Therefore, developing a facile yet effective PSM for modulating COFs' properties without altering the original geometry and/or structure is a challenge.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, Zhejiang, PR China. Electronic address:
The sluggish kinetics of the oxygen evolution reaction (OER) necessitate the use of efficient, non-precious metal catalysts. This work reports the rational design of an indium-doped bimetallic metal-organic framework (MOF-74-CoIn) as a precatalyst, achieved through post-synthetic modification of MOF-74-Co. Structural and spectroscopic analyses confirm that In(III) incorporation induces CoO bond contraction while preserves the overall structural integrity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Key Laboratory of Magnetic Molecules and Magnetic Information Material of Ministry of Education, School of Chemistry and Material Science, Shanxi Normal University, Taiyuan, 030006, P.R. China.
The strategic modulation of proton transport kinetics and precise control of migration energy barriers in metal-organic frameworks (MOFs) are essential for developing next-generation proton conductors. Inspired by biological proton channels, this study introduces a dynamic regulation strategy by keto-enol tautomerism to reconcile the intrinsic trade-off between low activation energy (E) and sustained proton mobility. We successfully construct a hierarchical proton conductive system (denoted as FU@MOF-808-SOH) by integrating 5-fluorouracil (5-FU) molecules into sulfonic-functionalized MOF-808 through a two-step post-synthetic modification.
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