The mechanochemical synthesis of all cobalt tellurides' phases is demonstrated in this work. The samples had their structural, microstructural, and magnetic characterizations performed by X-ray powder diffraction, transmission electron microscopy, and magnetometry techniques. The initial atomic stoichiometries tested of CoTe and CoTe resulted in the synthesis of the γ-CoTe (marcasite), α-CoTe 3̄ (pyrite), α-CoTe 3̄1 (CdI-like), and β-CoTe 6/ phases with different weight proportions in the sample. Modeling of the X-ray diffractograms employed conventional double-Voigt and crystallite shape-anisotropy DV approaches to show that the volumetric diameter average and true crystallite size of the diffraction domains are in the range of tens of nanometers. Transmission electron microscopy measurements also allowed distribution counting of the crystallite sizes maximum caliper diameter. Electron diffraction experiments presented comparable structural parameters with Rietveld the analysis of the Debye rings. A model using the Langevin approaches showed the phases to present both ferromagnetic and superparamagnetic contributions attributed to weakly-interacting metallic Co grains with magnetic domain sizes ranging between 2.3 and 4.0 nm. The phases' evolution with storage time was analyzed over two years and revealed to be stable regarding their structural and microstructural properties.
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http://dx.doi.org/10.1039/d2ra05757c | DOI Listing |
ChemSusChem
January 2025
Comenius University FNS: Univerzita Komenskeho v Bratislave Prirodovedecka fakulta, Organic chemistry, Mlynska dolina, Ilkovicova 6, 84215, Bratislava, SLOVAKIA.
Cross-coupling reactions are indispensable for the construction of complex molecular scaffolds. In this work, we developed a sustainable methodology for the cross-coupling reaction of arene thianthrenium salts with aryl boronic acids, which can be effectively realized under mechanochemical conditions. Liquid-assisted grinding (LAG) enabled fast and high-yielding synthesis of a range of biaryls via Pd/RuPhos-catalyzed cross-coupling.
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January 2025
Universita degli study di cagliari, Dipartimento di Scienze Chimiche e Geologiche, Cittadella Universitaria, SS 554 bivio per Sestu, 09042, Monserrato, ITALY.
Solvent-free techniques have gained considerable attention in recent years due to their environmental advantages and potential to enable chemical reactivities beyond the reach of traditional solution-based methods. Mechanochemistry has emerged as a groundbreaking approach to drive sustainable chemical processes. Despite its promise, some challenges still need to be explored, including the overlooked issue of material leaching during grinding, a phenomenon in which components from milling media or reaction vessels, such as stainless steel, unintentionally alter reaction outcomes.
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January 2025
Universidad de Antioquia Facultad de Ciencias Exactas y Naturales, Instituto de Química, Calle 70 No 52-21, Medellín, NA, Medellín, COLOMBIA.
In recent years, mechanosynthesis of peptides through either chemical or enzymatic routes has been accomplished. In part, this advancement has been driven due to the organocatalytic properties of peptide-based biomaterials. In this work, we report the merging of chemical and enzymatic protocols under mechanochemical conditions to synthesize peptide materials based on L-proline and L-phenylalanine.
View Article and Find Full Text PDFAdv Mater
January 2025
Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang, 325035, China.
Closed-loop transformation of raw materials into high-value-added products is highly desired for the sustainable development of the society but is seldom achieved. Here, a low-cost, solvent-free and "zero-waste" mechanochemical protocol is reported for the large-scale preparation of cathode materials for sodium-ion batteries (SIBs). This process ensures full utilization of raw materials, effectively reduces water consumption, and simplifies the operating process.
View Article and Find Full Text PDFMol Pharm
January 2025
Department of Industrial and Molecular Pharmaceutics, College of Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, Indiana 47907, United States.
Lumefantrine (LMF) is a low-solubility antimalarial drug that cures acute, uncomplicated malaria. It exerts its pharmacological effects against erythrocytic stages of spp. and prevents malaria pathogens from producing nucleic acid and protein, thereby eliminating the parasites.
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