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Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives

[Image: see text] This work focussed on the synthesis of a new catalytic material isinglass (IG)-based Fe(3)O(4)@GA@IG core/shell magnetic nanoparticles and the investigation of its catalytic activity in two important multicomponent reactions. Fe(3)O(4) nanoparticles were prepared using a simple cop...

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Autores principales: Pourian, Elham, Javanshir, Shahrzad, Dolatkhah, Zahra, Molaei, Shiva, Maleki, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641881/
https://www.ncbi.nlm.nih.gov/pubmed/31458714
http://dx.doi.org/10.1021/acsomega.8b00379
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author Pourian, Elham
Javanshir, Shahrzad
Dolatkhah, Zahra
Molaei, Shiva
Maleki, Ali
author_facet Pourian, Elham
Javanshir, Shahrzad
Dolatkhah, Zahra
Molaei, Shiva
Maleki, Ali
author_sort Pourian, Elham
collection PubMed
description [Image: see text] This work focussed on the synthesis of a new catalytic material isinglass (IG)-based Fe(3)O(4)@GA@IG core/shell magnetic nanoparticles and the investigation of its catalytic activity in two important multicomponent reactions. Fe(3)O(4) nanoparticles were prepared using a simple coprecipitation method and then coated with IG consisting predominantly of the protein collagen in the presence of glutaraldehyde as a cross-linking agent. The obtained hybrid material has been characterized by Fourier transform infrared analysis, scanning electron microscopy, transmission electron microscopy (TEM), vibrating sample magnetometry, energy-dispersive X-ray, X-ray diffraction (XRD), and Brunauer–Emmett–Teller analyses. The results of XRD analysis implied that the prepared nanocomposite consists of two compounds of crystalline magnetite and amorphous IG, and the formation of its core/shell structure had been confirmed by TEM images. The catalytic performance of the as-prepared core/shell bionanocatalyst was evaluated for the first time in the synthesis of 1,4-dihydropyridine and 4H-pyran derivatives under sonication in ethanol. This core/shell structure because of the superparamagnetic property of Fe(3)O(4) and unique properties of IG as a bifunctional biocatalyst offers a high potential for many catalytic applications. Recycling study revealed that no significant decrease in the catalytic activity was observed even after six runs.
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spelling pubmed-66418812019-08-27 Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives Pourian, Elham Javanshir, Shahrzad Dolatkhah, Zahra Molaei, Shiva Maleki, Ali ACS Omega [Image: see text] This work focussed on the synthesis of a new catalytic material isinglass (IG)-based Fe(3)O(4)@GA@IG core/shell magnetic nanoparticles and the investigation of its catalytic activity in two important multicomponent reactions. Fe(3)O(4) nanoparticles were prepared using a simple coprecipitation method and then coated with IG consisting predominantly of the protein collagen in the presence of glutaraldehyde as a cross-linking agent. The obtained hybrid material has been characterized by Fourier transform infrared analysis, scanning electron microscopy, transmission electron microscopy (TEM), vibrating sample magnetometry, energy-dispersive X-ray, X-ray diffraction (XRD), and Brunauer–Emmett–Teller analyses. The results of XRD analysis implied that the prepared nanocomposite consists of two compounds of crystalline magnetite and amorphous IG, and the formation of its core/shell structure had been confirmed by TEM images. The catalytic performance of the as-prepared core/shell bionanocatalyst was evaluated for the first time in the synthesis of 1,4-dihydropyridine and 4H-pyran derivatives under sonication in ethanol. This core/shell structure because of the superparamagnetic property of Fe(3)O(4) and unique properties of IG as a bifunctional biocatalyst offers a high potential for many catalytic applications. Recycling study revealed that no significant decrease in the catalytic activity was observed even after six runs. American Chemical Society 2018-05-08 /pmc/articles/PMC6641881/ /pubmed/31458714 http://dx.doi.org/10.1021/acsomega.8b00379 Text en Copyright © 2018 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 Pourian, Elham
Javanshir, Shahrzad
Dolatkhah, Zahra
Molaei, Shiva
Maleki, Ali
Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives
title Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives
title_full Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives
title_fullStr Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives
title_full_unstemmed Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives
title_short Ultrasonic-Assisted Preparation, Characterization, and Use of Novel Biocompatible Core/Shell Fe(3)O(4)@GA@Isinglass in the Synthesis of 1,4-Dihydropyridine and 4H-Pyran Derivatives
title_sort ultrasonic-assisted preparation, characterization, and use of novel biocompatible core/shell fe(3)o(4)@ga@isinglass in the synthesis of 1,4-dihydropyridine and 4h-pyran derivatives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641881/
https://www.ncbi.nlm.nih.gov/pubmed/31458714
http://dx.doi.org/10.1021/acsomega.8b00379
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