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Reductive Oligomerization of Nitroaniline Catalyzed by Fe(3)O(4) Spheres Decorated with Group 11 Metal Nanoparticles
[Image: see text] The present work demonstrates a simple and sustainable method for forming azo oligomers from low-value compounds such as nitroaniline. The reductive oligomerization of 4-nitroaniline was achieved via azo bonding using nanometric Fe(3)O(4) spheres doped with metallic nanoparticles (...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979374/ https://www.ncbi.nlm.nih.gov/pubmed/36873030 http://dx.doi.org/10.1021/acsomega.2c06326 |
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author | Huerta-Aguilar, Carlos Alberto Srivastava, Rajendra Arenas-Alatorre, Jesús A. Thangarasu, Pandiyan |
author_facet | Huerta-Aguilar, Carlos Alberto Srivastava, Rajendra Arenas-Alatorre, Jesús A. Thangarasu, Pandiyan |
author_sort | Huerta-Aguilar, Carlos Alberto |
collection | PubMed |
description | [Image: see text] The present work demonstrates a simple and sustainable method for forming azo oligomers from low-value compounds such as nitroaniline. The reductive oligomerization of 4-nitroaniline was achieved via azo bonding using nanometric Fe(3)O(4) spheres doped with metallic nanoparticles (Cu NPs, Ag NPs, and Au NPs), which were characterized by different analytical methods. The magnetic saturation (M(s)) of the samples showed that they are magnetically recoverable from aqueous environments. The effective reduction of nitroaniline followed pseudo-first-order kinetics, reaching a maximum conversion of about 97%. Fe(3)O(4)-Au is the best catalyst, its a reaction rate (k(Fe(3)O(4)-Au) = 0.416 mM L(–1) min(–1)) is about 20 times higher than that of bare Fe(3)O(4) (k(Fe(3)O(4)) = 0.018 mM L(–1) min(–1)). The formation of the two main products was determined by high-performance liquid chromatography-mass spectrometry (HPLC-MS), evidencing the effective oligomerization of NA through N = N azo linkage. It is consistent with the total carbon balance and the structural analysis by density functional theory (DFT)-based total energy. The first product, a six-unit azo oligomer, was formed at the beginning of the reaction through a shorter, two-unit molecule. The nitroaniline reduction is controllable and thermodynamically viable, as shown in the computational studies. |
format | Online Article Text |
id | pubmed-9979374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99793742023-03-03 Reductive Oligomerization of Nitroaniline Catalyzed by Fe(3)O(4) Spheres Decorated with Group 11 Metal Nanoparticles Huerta-Aguilar, Carlos Alberto Srivastava, Rajendra Arenas-Alatorre, Jesús A. Thangarasu, Pandiyan ACS Omega [Image: see text] The present work demonstrates a simple and sustainable method for forming azo oligomers from low-value compounds such as nitroaniline. The reductive oligomerization of 4-nitroaniline was achieved via azo bonding using nanometric Fe(3)O(4) spheres doped with metallic nanoparticles (Cu NPs, Ag NPs, and Au NPs), which were characterized by different analytical methods. The magnetic saturation (M(s)) of the samples showed that they are magnetically recoverable from aqueous environments. The effective reduction of nitroaniline followed pseudo-first-order kinetics, reaching a maximum conversion of about 97%. Fe(3)O(4)-Au is the best catalyst, its a reaction rate (k(Fe(3)O(4)-Au) = 0.416 mM L(–1) min(–1)) is about 20 times higher than that of bare Fe(3)O(4) (k(Fe(3)O(4)) = 0.018 mM L(–1) min(–1)). The formation of the two main products was determined by high-performance liquid chromatography-mass spectrometry (HPLC-MS), evidencing the effective oligomerization of NA through N = N azo linkage. It is consistent with the total carbon balance and the structural analysis by density functional theory (DFT)-based total energy. The first product, a six-unit azo oligomer, was formed at the beginning of the reaction through a shorter, two-unit molecule. The nitroaniline reduction is controllable and thermodynamically viable, as shown in the computational studies. American Chemical Society 2023-02-13 /pmc/articles/PMC9979374/ /pubmed/36873030 http://dx.doi.org/10.1021/acsomega.2c06326 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Huerta-Aguilar, Carlos Alberto Srivastava, Rajendra Arenas-Alatorre, Jesús A. Thangarasu, Pandiyan Reductive Oligomerization of Nitroaniline Catalyzed by Fe(3)O(4) Spheres Decorated with Group 11 Metal Nanoparticles |
title | Reductive Oligomerization
of Nitroaniline Catalyzed
by Fe(3)O(4) Spheres Decorated with Group 11 Metal
Nanoparticles |
title_full | Reductive Oligomerization
of Nitroaniline Catalyzed
by Fe(3)O(4) Spheres Decorated with Group 11 Metal
Nanoparticles |
title_fullStr | Reductive Oligomerization
of Nitroaniline Catalyzed
by Fe(3)O(4) Spheres Decorated with Group 11 Metal
Nanoparticles |
title_full_unstemmed | Reductive Oligomerization
of Nitroaniline Catalyzed
by Fe(3)O(4) Spheres Decorated with Group 11 Metal
Nanoparticles |
title_short | Reductive Oligomerization
of Nitroaniline Catalyzed
by Fe(3)O(4) Spheres Decorated with Group 11 Metal
Nanoparticles |
title_sort | reductive oligomerization
of nitroaniline catalyzed
by fe(3)o(4) spheres decorated with group 11 metal
nanoparticles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979374/ https://www.ncbi.nlm.nih.gov/pubmed/36873030 http://dx.doi.org/10.1021/acsomega.2c06326 |
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