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Copper is among the most-used metals in our daily life and in industry, but its thermal and electronic conductivities may be affected by the corrosion occurring in practical use. Molecular passivation represents a promising method to enhance the corrosion resistance of copper, but so far, it remains challenging to passivate the surface of copper with a robust nanolayer of small molecules. Here, we apply aryl diazonium grafting as a facile and efficient method to enhance the chemical resistance of copper materials of different sizes and shapes under mild conditions. We take advantage of the instability of aryl diazonium salts to passivate the surface of copper with a nanolayer of aryl groups, which endows copper not just with enhanced thermostability but also with improved corrosion resistance against solutions of alkali, hydrogen peroxide, sulfide, and salt. With an auxiliary ligand, the corrosion rate of aryl-modified copper foil can be as low as 3.12 μm yr in alkaline media, corresponding to an inhibition efficiency of 95.9%. We expect that the ease of operation, the versatility of diazonium chemistry, and the high inhibition efficiency of aryl passivation nanolayers will make our protocol applicable for Cu passivation in practical uses.
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http://dx.doi.org/10.1021/acs.langmuir.5c01037 | DOI Listing |
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September 2025
Department of Chemistry, Indian Institute of Technology, Kanpur, Uttar Pradesh, 208016, India.
Redox-active organic-inorganic hybrid electrode materials are promising candidates for eco-friendly, high-energy-density supercapacitors. The synergy between organic and inorganic components in energy storage devices has attracted considerable interest due to their complementary attributes, including flexibility, long-term stability, and high conductivity. This study presents an innovative approach for synthesizing an organic-inorganic active electrode material by grafting diazonium salts of 8-aminoquinoline (8-AQ-N ) onto CuFeO nanoparticle (NP) surfaces.
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September 2025
Key Laboratory of Precision and Intelligent Chemistry, Hefei National Research Center for Physical Sciences at the Microscale, Department of Materials Science and Engineering, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026, P. R. China.
Photocatalytic nitrogen reduction offers a sustainable approach to ammonia production. Here, we develop covalently functionalized 2D fullerene (C) networks through aryl diazonium chemistry, as verified by neutron scattering, spectroscopic analysis, and atomic force microscopy (AFM). The functionalized 2D fullerenes (e.
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August 2025
Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, Mülheim an der Ruhr 45470, Germany.
Herein, we report a straightforward methodology for direct deaminative cyanation of anilines via aryl diazonium salts as fleeting intermediates. The approach leverages the kinetic stability of nitrate and copper cyanide, iron's ability to facilitate nitrate reduction, and appropriate relative rates to ensure the product-forming kinetic reaction pathway despite several thermodynamically favored, undesired reactions. We present insight into the previously unappreciated nitrate reduction mechanism by simple sulfur-based reductants, such as SO.
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August 2025
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208, United States.
Surface-capping molecular ligands are an integral part of virtually all colloidal inorganic nanoparticles that are chemically synthesized. The rational design of nanoparticle-adsorbate hybrid materials with specifically targeted properties and functionalities relies crucially on our understanding of ligand chemistry at the nanoparticle surfaces. Organic ligand molecules can interact covalently with metal surfaces through chemisorption using a variety of surface-binding moieties, most commonly thiol groups, to form self-assembled monolayers of monomeric adsorbates when reaching the saturated surface-coverage.
View Article and Find Full Text PDFJ Org Chem
August 2025
College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China.
The Sandmeyer reaction is a key method for synthesizing aryl halides but often requires complex procedures and large solvent volumes. This study introduces a mechanoredox system using ball milling to activate piezoelectric BaTiO, enabling solvent-minimized, metal-catalyst-free halogenation of aryl diazonium salts under air. The method features a broad substrate scope, scalability, and recyclable piezoelectric materials without significant activity loss.
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