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This study presents the successful immobilization of a methotrexate-palladium complex onto the surface of magnetic CoFeO nanoparticles through a simple and cost-efficient process. The environmentally friendly heterogeneous catalyst was comprehensively characterized using thermogravimetric analysis (TGA), energy dispersive spectroscopy (EDS), scanning electron microscopy (SEM), X-ray diffraction (XRD), vibrating sample magnetometry (VSM), inductively coupled plasma (ICP) atomic absorption spectroscopy, and Fourier transform infrared (FT-IR) spectroscopy. The catalyst demonstrated outstanding catalytic efficiency, achieving a 98% yield in the reduction of nitroarenes and facilitating the synthesis of diaryl sulfide derivatives under green conditions. Offering a practical and economical approach for immobilizing palladium-methotrexate complexes, this method serves as a promising alternative to conventional techniques in diaryl sulfide synthesis. Its advantages include easy recovery and reusable performance over four successive cycles. This catalyst holds significant potential for applications in both pharmaceutical and chemical industries.
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http://dx.doi.org/10.1038/s41598-025-12436-2 | DOI Listing |
Sci Rep
September 2025
University Name: Arnold and Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, NY, USA.
This study presents the successful immobilization of a methotrexate-palladium complex onto the surface of magnetic CoFeO nanoparticles through a simple and cost-efficient process. The environmentally friendly heterogeneous catalyst was comprehensively characterized using thermogravimetric analysis (TGA), energy dispersive spectroscopy (EDS), scanning electron microscopy (SEM), X-ray diffraction (XRD), vibrating sample magnetometry (VSM), inductively coupled plasma (ICP) atomic absorption spectroscopy, and Fourier transform infrared (FT-IR) spectroscopy. The catalyst demonstrated outstanding catalytic efficiency, achieving a 98% yield in the reduction of nitroarenes and facilitating the synthesis of diaryl sulfide derivatives under green conditions.
View Article and Find Full Text PDFBeilstein J Org Chem
May 2025
Department of Chemistry, University of Pavia, Viale Taramelli 12, 27100 Pavia, Italy.
We investigated the potential application of six types of carbon dots (CDs) obtained from different organic sources as photoreductants. Such carbon nanomaterials were synthesized by two different approaches, either hydrothermal or pyrolytic, from citric acid and glucose as the starting organic substrates. On the other hand, carbon dots deriving from fishery waste (bass scales) and fruit processing waste (blackberries) have been also prepared.
View Article and Find Full Text PDFRSC Adv
April 2025
Institute of Advanced Technology, University of Science and Technology of China Hefei 230000 China
An efficient iodine-catalyzed thio-arylation reaction of aniline was developed under electrochemical conditions. A variety of diaryl sulfide compounds can be obtained under metal-free and chemical oxidant-free conditions. The reaction features a broad substrate scope, regulation of product distribution, and scalable preparation.
View Article and Find Full Text PDFJ Org Chem
March 2025
Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Institute of Science Tokyo, Nagatsuta-cho 4259-G-1, Midori-ku, Yokohama 226-8501, Japan.
As cationic functional groups with excellent alkaline resistance that are potentially applicable to building blocks of robust anion exchange membrane (AEM) materials for water splitting and fuel cell modules, we describe the synthesis of triarylsulfonium () salts bearing sterically demanding substituents by the reaction of arynes with diaryl sulfides/sulfoxides and by the Friedel-Crafts reaction of diaryl sulfoxides. The cations possessing three substituted benzene rings, such as tris(2,5-dimethylphenyl)sulfonium and bis(2,5-dimethylphenyl)mesitylsulfonium, were effectively produced through the appropriate choice of reactions and reagents. The alkaline stability of the cations thus obtained was evaluated from their time-course H NMR spectra in 1 M KOH/CDOD, from which the alkaline resistance of the cations increased dramatically as the steric bulkiness of the aromatic substituents attached to the cations increased.
View Article and Find Full Text PDFSci Rep
October 2024
Medical laboratory technique college, the Islamic University, Najaf, Iraq.
This article is devoted to the synthesis of a new magnetic palladium catalyst that has been immobilized on A-TT-Pd coated-magnetic FeO nanoparticles. Such surface functionalization of magnetic particles is a promising method to bridge the gap between heterogeneous and homogeneous catalysis approaches. The structure, morphology, and physicochemical properties of the particles were characterized through different analytical techniques, including TEM, FT-IR, XRD, SEM, EDS, TGA-DTG, ICP, and VSM techniques.
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