Abstract:In this study, a new precursor was synthesized form the reaction of melamine and chloroacetonitrile. By using this pre‐material, the new mesoporous triazine based‐carbon material was prepared during ionothermal process with the help of ZnCl2, and used as the excellent support for silver nano‐particles. The new nano‐catalyst was named Ag/mCTF(mesoporous Carbon Triazine Framework), and fully characterized by various analytical methods including Fourier transformed infrared spectroscopy (FT‐IR), field emission sc… Show more
Carbon materials play important roles as catalysts or catalyst supports for reduction reactions owing to their high porosity, large specific surface area, great electron conductivity, and excellent chemical stability. In this paper, a mesoporous N-doped carbon substrate (exhibited as N–C) has been synthesized by ionothermal carbonization of glucose in the presence of histidine. The N–C substrate was modified by Fe3O4 nanoparticles (N–C/Fe3O4), and then Pd nanoparticles were stabilized on the magnetic substrate to synthesize an eco-friendly Pd catalyst with high efficiency, magnetic, reusability, recoverability, and great stability. To characterize the Pd/Fe3O4–N–C nanocatalyst, different microscopic and spectroscopic methods such as FT-IR, XRD, SEM/EDX, and TEM were applied. Moreover, Pd/Fe3O4–N–C showed high catalytic activity in reducing nitroaromatic compounds in water at ambient temperatures when NaBH4 was used as a reducing agent. The provided nanocatalyst's great catalytic durability and power can be attributed to the synergetic interaction among well-dispersed Pd nanoparticles and N-doped carbonaceous support.
Carbon materials play important roles as catalysts or catalyst supports for reduction reactions owing to their high porosity, large specific surface area, great electron conductivity, and excellent chemical stability. In this paper, a mesoporous N-doped carbon substrate (exhibited as N–C) has been synthesized by ionothermal carbonization of glucose in the presence of histidine. The N–C substrate was modified by Fe3O4 nanoparticles (N–C/Fe3O4), and then Pd nanoparticles were stabilized on the magnetic substrate to synthesize an eco-friendly Pd catalyst with high efficiency, magnetic, reusability, recoverability, and great stability. To characterize the Pd/Fe3O4–N–C nanocatalyst, different microscopic and spectroscopic methods such as FT-IR, XRD, SEM/EDX, and TEM were applied. Moreover, Pd/Fe3O4–N–C showed high catalytic activity in reducing nitroaromatic compounds in water at ambient temperatures when NaBH4 was used as a reducing agent. The provided nanocatalyst's great catalytic durability and power can be attributed to the synergetic interaction among well-dispersed Pd nanoparticles and N-doped carbonaceous support.
“…Particularly, doping carbon with two or several heteroatoms can further improve the catalytic performance in different organic and electrochemical reactions due to the synergistic effects between various heteroatoms and metal NPs and can significantly inhibit the agglomeration, leaching, and corrosion of metal NPs. [36][37][38] In continuation of our studies on the development of heteroatom-doped carbon materials and their application as supports or heterogeneous catalysts, [39][40][41][42][43][44][45] in this paper, we report the preparation of Ag NPs decorated on selenium and nitrogen co-doped mesoporous carbon (Ag/m-SeNC) by pyrolyzing cheap raw materials of glucose, ammonium chloride (NH 4 Cl), and selenium dioxide (SeO 2 ) as the carbon, nitrogen, and selenium sources and AgNO 3 as a metal precursor. The resultant Se,N-carbon was used as a support for the immobilization of Ag NPs to fabricate a stable nanocatalyst Ag/m-SeNC.…”
Section: Introductionmentioning
confidence: 95%
“…In continuation of our studies on the development of heteroatom‐doped carbon materials and their application as supports or heterogeneous catalysts, [ 39–45 ] in this paper, we report the preparation of Ag NPs decorated on selenium and nitrogen co‐doped mesoporous carbon (Ag/m‐SeNC) by pyrolyzing cheap raw materials of glucose, ammonium chloride (NH 4 Cl), and selenium dioxide (SeO 2 ) as the carbon, nitrogen, and selenium sources and AgNO 3 as a metal precursor. The resultant Se,N‐carbon was used as a support for the immobilization of Ag NPs to fabricate a stable nanocatalyst Ag/m‐SeNC.…”
Silver nanoparticles (Ag NPs) supported on selenium and nitrogen co‐doped mesoporous carbon were prepared through pyrolysis of glucose, ammonium chloride (NH4Cl), and selenium dioxide (SeO2) as the carbon, nitrogen, and selenium sources, followed by a chemical reduction strategy. The synthesized Ag/m‐SeNC could catalyze the hydrogenation of a series of nitroaromatics to corresponding amines effectively in an aqueous solution in the presence of NaBH4 as a hydrogen donor. Besides, this heterogeneous nanocatalyst could be simply reused four successive times without significant reduction in activity and selectivity.
“…In addition, they are used in the manufacture of electrical circuits [18] and also as an anti-corrosion coating for copper [19]. Imidazole substitutes have recently been used as secondary catalysts in the chemical industries, especially in organic chemical reactions [20].…”
The aim of this work was to create new ligand complexes and evaluate their effectiveness against certain strains of bacteria. A Brucker Tensor 27co FTIR spectrophotometer was used to record the infrared spectra. Elemental analysis (C, H, N) was carried out on an AA670 atomic absorption spectrophotometer to determine mineral content, and the conductivity of PCM3 Jenway was measured to record electronic spectra. The ligand was prepared, that possessed physical constants and spectroscopic properties. The complexes [M(L)2Cl2] and [M(L)4Cl2] were also prepared, where M=Mn(II), Co(II), Ni(II), Cu(II), and Zn(II), which were synthesized by direct reaction of the above ligand with metal chlorides in (2:1) or (4:1) (Ligand : metal) molar ratio in the ethanol medium. The ligand compound 4-(2-(benzo-1,3-dioxol-5-yl)-4,5-diphenyl-2,5-dihydro1H-imidazol-1-yl)aniline (L) was obtained. The prepared complexes were shown by elemental analysis, spectroscopic studies (FTIR, UV/vis), 1H-NMR measurement, conductivity measurements, and electron spectrometry value, which indicate the presence of tetrahedral and octahedral geometry around the metal ions. The biological antibacterial activity of the compounds and complexes has been demonstrated against specific strains of G+ Staph. aureus and G− Bacillus. The bonding compound L coordinates the metal in a tetrahedral and octahedral N-M-N manner. The compound and its complexes had activity against specific strains of bacteria. The ligand (L1) and the complex (3) had a greater effect on different types of bacteria than the rest of the complexes, which had a lower efficiency rate.
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