The Fe ion is the most important element in environmental systems and plays a fundamental role in biological processes. Iron deficiency can result in diseases and highly selective and sensitive detection of trace Fe has become a hot topic. A novel two-dimensional Zn coordination framework, poly[[μ-4,4'-bis(2-methylimidazol-1-yl)diphenyl ether-κN:N](μ-4,4'-sulfonyldibenzoato-κO:O')zinc(II)], [Zn(CHOS)(CHNO)] or [Zn(SDBA)(BMIOPE)], (I), where HSDBA is 4,4'-sulfonyldibenzoic acid and BMIOPE is 4,4'-bis(2-methylimidazol-1-yl)diphenyl ether, has been prepared and characterized by IR, elemental analysis, thermal analysis and X-ray diffraction analysis, the latter showing that the coordination polymer exhibits a threefold interpenetrating two-dimensional 4-sql network. In addition, it displays a highly selective and sensitive sensing for Fe ions in aqueous solution.
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http://dx.doi.org/10.1107/S2053229619008635 | DOI Listing |
Angew Chem Int Ed Engl
September 2024
College of Chemistry and Pingyuan Laboratory, Zhengzhou Key Laboratory of Elastic Sealing Materials, Zhengzhou University, Zhengzhou, 450001, China.
Structural adhesives that do not require heating are in high demand in the automotive and electronics industries. However, it remains a challenge to develop robust adhesives that rapidly achieve super adhesion near ambient temperature. Herein, a room-temperature curable, fast-bonding, and super strong epoxy-based structural adhesive was designed from the perspective of cross-scale structure, which lies in threefold pivotal aspects: (i) high branching topology of glycerol carbonate-capped polyurethane (PUGC) increases the kinetics of the ring-opening reaction, contributing to fast crosslinking and the formation of abundant urethane and hydroxyl moieties; (ii) asynchronous crosslinking of epoxy and PUGC synergistically induces phase separation of PUGC within the epoxy resin and the resulting PUGC domains surrounded by interpenetrated shell serves to efficiently toughen the matrix; (iii) abundant dynamic hydrogen bonds including urethane and hydroxyl moieties, along with the elastomeric PUGC domains, dissipate energy of shearing force.
View Article and Find Full Text PDFChem Sci
January 2024
Department of Applied Chemistry, Faculty of Science Division I, Tokyo University of Science 1-3 Kagurazaka Shinjuku-ku Tokyo 162-8601 Japan
Molecules
January 2024
Department of Chemistry, Chung Yuan Christian University, Chung Li, Taoyuan City 320, Taiwan.
Reactions of '-(3-methylpyridyl)oxalamide (), ,'-(3-methylpyridyl)adipoamide () and ,'-(3-methylpyridyl)sebacoamide () with tricarboxylic acids and Cu(II) salts afforded {[Cu()(1,3,5-HBTC)]·HO} (1,3,5-HBTC = 1,3,5-benzenetricarboxylic acid), , {[Cu()(1,3,5-BTC)(HO)]·6.5HO}, , [Cu()(1,3,5-HBTB)] (1,3,5-HBTB = 1,3,5-tri(4-carboxyphenyl)benzene), , [Cu()(OH)(1,3,5-BTC)], , {[Cu()(1,3,5-BTB)]·2.5MeOH·2HO}, , and {[Cu()(1,3,5-BTB) ]·DMF·2HO}, , which have been structurally characterized by using single crystal X-ray crystallography.
View Article and Find Full Text PDFDalton Trans
June 2023
Inorganic Materials & Catalysis Division, CSIR-Central Salt & Marine Chemicals Research Institute, Bhavnagar, Gujarat 364002, India.
Concerning environmentally benign catalysis with reduced chemical usage, less energy consumption, and waste minimization, metal-organic frameworks (MOFs) with spatially isolated task-specific functionalities not only execute atom-economic important reactions but also enable size-exclusive catalysis at the interface of structure-function synergy. Herein, we synthesized a bipillar-layer Co(II) MOF from the dicarboxylate ligand and carboxamide moiety grafted pyridyl linker. The framework contains a [Co(COO)N] secondary building unit (SBU) and shows excellent hydrolytic stability due to ample non-covalent interactions among the highly conjugated aromatic struts.
View Article and Find Full Text PDFACS Appl Mater Interfaces
May 2023
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
Development of the multifaceted metal-organic framework (MOF) with in situ engineered task-specific sites can promise proficient oxygen evolution reaction (OER) and high-temperature adsorption cum mild-condition fixation of CO. In fact, effective assimilation of these attributes onto a single material with advance performance characteristics is practically imperative in view of renewable energy application and carbon-footprint reduction. Herein, we developed a three-fold interpenetrated robust Co(II) framework that embraces both redox-active and hydrogen-bond donor moieties inside the microporous channel.
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