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Bimetallic Nanoparticles Anchored on Core–Shell Support as an Easily Recoverable and Reusable Catalytic System for Efficient Nitroarene Reduction
[Image: see text] We report an easily recoverable and reusable versatile magnetic catalyst (Fe(3)O(4)@CS_AgNi, where CS = chitosan) for organic reduction reactions. The catalytic system is prepared by dispersing AgNi bimetallic nanoparticles on the magnetite core–shell (Fe(3)O(4)@CS). The as-synthes...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648521/ https://www.ncbi.nlm.nih.gov/pubmed/31460014 http://dx.doi.org/10.1021/acsomega.9b01023 |
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author | Antony, Rajendran Marimuthu, Rajendiran Murugavel, Ramaswamy |
author_facet | Antony, Rajendran Marimuthu, Rajendiran Murugavel, Ramaswamy |
author_sort | Antony, Rajendran |
collection | PubMed |
description | [Image: see text] We report an easily recoverable and reusable versatile magnetic catalyst (Fe(3)O(4)@CS_AgNi, where CS = chitosan) for organic reduction reactions. The catalytic system is prepared by dispersing AgNi bimetallic nanoparticles on the magnetite core–shell (Fe(3)O(4)@CS). The as-synthesized catalyst has been characterized by spectroscopic techniques, such as IR, UV–vis, and X-ray photoelectron spectroscopy (XPS), and analytical tools, such as thermogravimetric analysis, powder X-ray diffraction, Brunauer–Emmett–Teller adsorption, FEG–scanning electron microscopy, high-resolution transmission electron microscopy (HR-TEM), inductively coupled plasma-atomic emission spectroscopy, and magnetic measurements. HR-TEM studies indicate the core–shell structure of Fe(3)O(4)@CS and confirm the presence of AgNi nanoparticles on the surface of Fe(3)O(4)@CS spheres. IR spectral and XPS studies lend evidence for the occurrence of a strong chemical interaction between the amino groups of CS and AgNi nanoparticles. The nano-catalyst Fe(3)O(4)@CS_AgNi rapidly reduces p-nitrophenol to p-aminophenol using NaBH(4) as the reductant within a few minutes under ambient conditions (as monitored by UV–visible spectroscopy). The utility of this catalytic system has also been extended to the reduction of other nitroarenes. A strong interaction between Fe(3)O(4)@CS and AgNi nanoparticles impedes the leaching of AgNi nanoparticles from the core–shell support, leading to excellent reusability of the catalyst. |
format | Online Article Text |
id | pubmed-6648521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66485212019-08-27 Bimetallic Nanoparticles Anchored on Core–Shell Support as an Easily Recoverable and Reusable Catalytic System for Efficient Nitroarene Reduction Antony, Rajendran Marimuthu, Rajendiran Murugavel, Ramaswamy ACS Omega [Image: see text] We report an easily recoverable and reusable versatile magnetic catalyst (Fe(3)O(4)@CS_AgNi, where CS = chitosan) for organic reduction reactions. The catalytic system is prepared by dispersing AgNi bimetallic nanoparticles on the magnetite core–shell (Fe(3)O(4)@CS). The as-synthesized catalyst has been characterized by spectroscopic techniques, such as IR, UV–vis, and X-ray photoelectron spectroscopy (XPS), and analytical tools, such as thermogravimetric analysis, powder X-ray diffraction, Brunauer–Emmett–Teller adsorption, FEG–scanning electron microscopy, high-resolution transmission electron microscopy (HR-TEM), inductively coupled plasma-atomic emission spectroscopy, and magnetic measurements. HR-TEM studies indicate the core–shell structure of Fe(3)O(4)@CS and confirm the presence of AgNi nanoparticles on the surface of Fe(3)O(4)@CS spheres. IR spectral and XPS studies lend evidence for the occurrence of a strong chemical interaction between the amino groups of CS and AgNi nanoparticles. The nano-catalyst Fe(3)O(4)@CS_AgNi rapidly reduces p-nitrophenol to p-aminophenol using NaBH(4) as the reductant within a few minutes under ambient conditions (as monitored by UV–visible spectroscopy). The utility of this catalytic system has also been extended to the reduction of other nitroarenes. A strong interaction between Fe(3)O(4)@CS and AgNi nanoparticles impedes the leaching of AgNi nanoparticles from the core–shell support, leading to excellent reusability of the catalyst. American Chemical Society 2019-05-24 /pmc/articles/PMC6648521/ /pubmed/31460014 http://dx.doi.org/10.1021/acsomega.9b01023 Text en Copyright © 2019 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 | Antony, Rajendran Marimuthu, Rajendiran Murugavel, Ramaswamy Bimetallic Nanoparticles Anchored on Core–Shell Support as an Easily Recoverable and Reusable Catalytic System for Efficient Nitroarene Reduction |
title | Bimetallic Nanoparticles Anchored on Core–Shell
Support as an Easily Recoverable and Reusable Catalytic System for
Efficient Nitroarene Reduction |
title_full | Bimetallic Nanoparticles Anchored on Core–Shell
Support as an Easily Recoverable and Reusable Catalytic System for
Efficient Nitroarene Reduction |
title_fullStr | Bimetallic Nanoparticles Anchored on Core–Shell
Support as an Easily Recoverable and Reusable Catalytic System for
Efficient Nitroarene Reduction |
title_full_unstemmed | Bimetallic Nanoparticles Anchored on Core–Shell
Support as an Easily Recoverable and Reusable Catalytic System for
Efficient Nitroarene Reduction |
title_short | Bimetallic Nanoparticles Anchored on Core–Shell
Support as an Easily Recoverable and Reusable Catalytic System for
Efficient Nitroarene Reduction |
title_sort | bimetallic nanoparticles anchored on core–shell
support as an easily recoverable and reusable catalytic system for
efficient nitroarene reduction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648521/ https://www.ncbi.nlm.nih.gov/pubmed/31460014 http://dx.doi.org/10.1021/acsomega.9b01023 |
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