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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 (...

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Autores principales: Huerta-Aguilar, Carlos Alberto, Srivastava, Rajendra, Arenas-Alatorre, Jesús A., Thangarasu, Pandiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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