Abstract:A novel polydentate ligand supported on Fe 3 O 4 @SiO 2 was designed and demonstrated for the synthesis of Cu nanorods. The Fe 3 O 4 @SiO 2 /EP.EN.EG@Cu was characterized using X-ray diffraction, thermogravimetric analysis, transmission electron microscopy, energy-dispersive X-ray spectroscopy and vibrating sample magnetometry. The Fe 3 O 4 @SiO 2 /EP.EN.EG@Cu showed excellent catalytic efficiency for the cross-coupling reaction of nitrogen-containing heterocycles with aryl halides. The catalyst could be effec… Show more
“…From our previous study, we found that successfully synthesized Fe 3 O 4 @SiO 2 /EP.EN.EG.Cu can be used as a highly efficient robust in the reduction of nitro compounds and Ullmann cross‐coupling reaction under mild conditions. This results encouraged the authors to study catalytic efficiency in other reaction, herein we report a simple and efficient methodology for the synthesis of 1,4‐disubstituted‐1,2,3‐triazole.…”
A magnetic nanostructured core–shell Fe3O4@SiO2/EP.EN.EG.Cu has used as an efficient heterogeneous catalyst for the synthesis of 1,4‐disubstituted 1,2,3‐triazole derivatives through click reaction, under mild reaction conditions. A variety of epoxides, alkyl or benzyl halides was used to afford the corresponding 1,4‐disubstituted 1,2,3‐triazoles. The catalyst could be easily separated by using an external magnet from the reaction mixture and reused seven times without significant loss of catalytic activity.
“…From our previous study, we found that successfully synthesized Fe 3 O 4 @SiO 2 /EP.EN.EG.Cu can be used as a highly efficient robust in the reduction of nitro compounds and Ullmann cross‐coupling reaction under mild conditions. This results encouraged the authors to study catalytic efficiency in other reaction, herein we report a simple and efficient methodology for the synthesis of 1,4‐disubstituted‐1,2,3‐triazole.…”
A magnetic nanostructured core–shell Fe3O4@SiO2/EP.EN.EG.Cu has used as an efficient heterogeneous catalyst for the synthesis of 1,4‐disubstituted 1,2,3‐triazole derivatives through click reaction, under mild reaction conditions. A variety of epoxides, alkyl or benzyl halides was used to afford the corresponding 1,4‐disubstituted 1,2,3‐triazoles. The catalyst could be easily separated by using an external magnet from the reaction mixture and reused seven times without significant loss of catalytic activity.
“…Preparation of Fe 3 O 4 @SiO 2 /EP.EN.EG@Cu. Reprinted with permission from Rajabzadeh et al [ 149 ] Copyright 2017 John Wiley and Sons…”
Section: Copper Nanocatalystsmentioning
confidence: 99%
“…EN.EG@Cu. Reprinted with permission from Rajabzadeh et al [149] Copyright 2017 John Wiley and Sons S C H E M E 1 9 N-arylation of different nitrogen-containing heterocycles with aryl halides catalyzed by Fe 3 O 4 @SiO 2 /EP.EN.EG@Cu S C H E M E 2 0 N-arylation of imidazole with different aryl halides using Fe-CuO S C H E M E 2 1 N-arylation of different heterocycles with 4-bromobenzonitrile using Fe-CuO T A B L E 6 Fe 3 O 4 @SiO 2 -DAQ-Cu (II)-catalyzed N-arylation of N(H)-heterocycles and amines with various aryl halides F I G U R E 6 Preparation of the maghemite-Cu nanocatalyst. Reprinted with permission from Sharma et al [152] Copyright 2015 John Wiley and Sons F I G U R E 7 Preparation of Cu/ascorbic acid@MNPs.…”
Section: Maghemite-cu Nanocatalysts (Magnetically Separable Cu Nanoca...mentioning
The development of various methodologies for the formation of carbon‐nitrogen bonds is one of the valuable tasks in the field of organic synthesis because the final products are extensively utilized in pharmaceuticals, biologically active compounds, and natural products. The utilization of nanosized metal catalysts with high surface energy, large surface‐to‐volume ratio, excellent thermal stability, and reactive morphology in C‐N cross‐coupling reactions has received considerable attention, in recent years. The excellent catalytic performance, the high yield of products, carrying out the reactions under relatively mild and ligand‐free conditions, and less toxicity to the environment, recoverability, and reusability of catalysts for several times without a remarkable degradation in activity are advantages of these nanocatalysts.
This review intends to summarize the latest progress in the fabrication of nanocatalysts and their applications in the construction of carbon‐nitrogen bonds via cross‐coupling reactions. Abundant nanocatalysts based on metal and metal oxide nanoparticles/complexes including copper, palladium, nickel, cobalt, silver, gold, zirconium, and zinc have successfully been applied in these reactions. Various aspects of the reactions, different strategies of fabrication of nanocatalysts, and their recyclability have been surveyed. Literature has been investigated from 2015 to 2021.
“…[ 1–7 ] Industry favors the application of heterogeneous catalysts over homogeneous processes in view of the ease of handling and simple work‐up and separations. [ 8–15 ] Because of the importance of environmental and economic issues, global scientific and industrial discoveries in the field of catalysts should use the principles of “Green Chemistry”. [ 16–23 ] Recovery and reusability which can be regarded as the two valuable keys attached to the catalytic reactions for the definition of sustainability indicate that a catalytic process follows the “Green Chemistry” principles.…”
In this work, L-lysine-Pd Complex, immobilized onto the surface of Fe 3 O 4 MNPs, was successfully prepared via simple and inexpensive procedure. The prepared nanocatalyst was considered as a robust and clean nano-reactor catalyst for the Suzuki and Heck CC Cross-Coupling reactions in water as the green condition. This eco-friendly heterogeneous catalyst was characterized by Fourier transform infrared spectroscopy (FT-IR), X-Ray Diffractometer (XRD), energy-dispersive X-ray spectroscopy (EDS), inductively coupled plasma atomic emission spectroscopy (ICP), X-ray mapping, BET, thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), scanning electron microscopy (SEM) and Transmission electron microscopy (TEM) techniques. The use of a green medium, easy separation and workup, excellent reusability of the nanocatalyst and short reaction time are some outstanding advantages of this method.
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