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Nickel(II) Nanoparticles Immobilized on EDTA-Modified Fe(3)O(4)@SiO(2) Nanospheres as Efficient and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling of Aryl Carbamates and Sulfamates
[Image: see text] A highly efficient and air-, thermal-, and moisture-stable nickel-based catalyst with excellent magnetic properties supported on silica-coated magnetic Fe(3)O(4) nanoparticles was successfully synthesized. It was well characterized by Fourier transform infrared spectroscopy, powder...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144170/ https://www.ncbi.nlm.nih.gov/pubmed/32280882 http://dx.doi.org/10.1021/acsomega.9b04450 |
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author | Dindarloo Inaloo, Iman Majnooni, Sahar Eslahi, Hassan Esmaeilpour, Mohsen |
author_facet | Dindarloo Inaloo, Iman Majnooni, Sahar Eslahi, Hassan Esmaeilpour, Mohsen |
author_sort | Dindarloo Inaloo, Iman |
collection | PubMed |
description | [Image: see text] A highly efficient and air-, thermal-, and moisture-stable nickel-based catalyst with excellent magnetic properties supported on silica-coated magnetic Fe(3)O(4) nanoparticles was successfully synthesized. It was well characterized by Fourier transform infrared spectroscopy, powder X-ray diffraction, transmission electron microscopy, field emission scanning electron microscopy, thermogravimetric analysis, dynamic light scattering (DLS), X-ray photoelectron spectroscopy, vibration sample magnetometry, energy-dispersive X-ray analysis, inductively coupled plasma analysis, and nitrogen adsorption–desorption isotherm analysis. The Suzuki–Miyaura coupling reaction between aryl carbamates and/or sulfamates with arylboronic acids was selected to demonstrate the catalytic activity and efficiency of the as-prepared magnetic nanocatalyst. Using the mentioned heterogeneous nanocatalyst in such reactions generated corresponding products in good to excellent yields in which the catalyst could easily be recovered from the reaction mixture with an external magnetic field to reuse directly for the next several cycles without significant loss of its activity. |
format | Online Article Text |
id | pubmed-7144170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71441702020-04-10 Nickel(II) Nanoparticles Immobilized on EDTA-Modified Fe(3)O(4)@SiO(2) Nanospheres as Efficient and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling of Aryl Carbamates and Sulfamates Dindarloo Inaloo, Iman Majnooni, Sahar Eslahi, Hassan Esmaeilpour, Mohsen ACS Omega [Image: see text] A highly efficient and air-, thermal-, and moisture-stable nickel-based catalyst with excellent magnetic properties supported on silica-coated magnetic Fe(3)O(4) nanoparticles was successfully synthesized. It was well characterized by Fourier transform infrared spectroscopy, powder X-ray diffraction, transmission electron microscopy, field emission scanning electron microscopy, thermogravimetric analysis, dynamic light scattering (DLS), X-ray photoelectron spectroscopy, vibration sample magnetometry, energy-dispersive X-ray analysis, inductively coupled plasma analysis, and nitrogen adsorption–desorption isotherm analysis. The Suzuki–Miyaura coupling reaction between aryl carbamates and/or sulfamates with arylboronic acids was selected to demonstrate the catalytic activity and efficiency of the as-prepared magnetic nanocatalyst. Using the mentioned heterogeneous nanocatalyst in such reactions generated corresponding products in good to excellent yields in which the catalyst could easily be recovered from the reaction mixture with an external magnetic field to reuse directly for the next several cycles without significant loss of its activity. American Chemical Society 2020-03-27 /pmc/articles/PMC7144170/ /pubmed/32280882 http://dx.doi.org/10.1021/acsomega.9b04450 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Dindarloo Inaloo, Iman Majnooni, Sahar Eslahi, Hassan Esmaeilpour, Mohsen Nickel(II) Nanoparticles Immobilized on EDTA-Modified Fe(3)O(4)@SiO(2) Nanospheres as Efficient and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling of Aryl Carbamates and Sulfamates |
title | Nickel(II) Nanoparticles Immobilized on EDTA-Modified
Fe(3)O(4)@SiO(2) Nanospheres as Efficient
and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling
of Aryl Carbamates and Sulfamates |
title_full | Nickel(II) Nanoparticles Immobilized on EDTA-Modified
Fe(3)O(4)@SiO(2) Nanospheres as Efficient
and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling
of Aryl Carbamates and Sulfamates |
title_fullStr | Nickel(II) Nanoparticles Immobilized on EDTA-Modified
Fe(3)O(4)@SiO(2) Nanospheres as Efficient
and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling
of Aryl Carbamates and Sulfamates |
title_full_unstemmed | Nickel(II) Nanoparticles Immobilized on EDTA-Modified
Fe(3)O(4)@SiO(2) Nanospheres as Efficient
and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling
of Aryl Carbamates and Sulfamates |
title_short | Nickel(II) Nanoparticles Immobilized on EDTA-Modified
Fe(3)O(4)@SiO(2) Nanospheres as Efficient
and Recyclable Catalysts for Ligand-Free Suzuki–Miyaura Coupling
of Aryl Carbamates and Sulfamates |
title_sort | nickel(ii) nanoparticles immobilized on edta-modified
fe(3)o(4)@sio(2) nanospheres as efficient
and recyclable catalysts for ligand-free suzuki–miyaura coupling
of aryl carbamates and sulfamates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144170/ https://www.ncbi.nlm.nih.gov/pubmed/32280882 http://dx.doi.org/10.1021/acsomega.9b04450 |
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