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Template-Less and Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic Application in Ipso-hydroxylation of Aryl Boronic Acids and the aza-Michael Reaction
[Image: see text] Due to its excellent physicochemical properties, CeO(2) has found great importance as an electrochemical and in electronics, photocatalysis, sensing, and heterogeneous catalysis. Herein, we report the surfactant-less and template-less synthesis of CeO(2) nanostructures by the hydro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685755/ https://www.ncbi.nlm.nih.gov/pubmed/36440121 http://dx.doi.org/10.1021/acsomega.2c04614 |
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author | Chandra Saikia, Tulan Borgohain, Xavy Iraqui, Saddam Rashid, Md. Harunar |
author_facet | Chandra Saikia, Tulan Borgohain, Xavy Iraqui, Saddam Rashid, Md. Harunar |
author_sort | Chandra Saikia, Tulan |
collection | PubMed |
description | [Image: see text] Due to its excellent physicochemical properties, CeO(2) has found great importance as an electrochemical and in electronics, photocatalysis, sensing, and heterogeneous catalysis. Herein, we report the surfactant-less and template-less synthesis of CeO(2) nanostructures by the hydrothermal method. The synthesized CeO(2) nanostructures have been characterized in detail by electron microscopy, spectroscopy, diffractometry, and other analytical methods. The XRD studies revealed the formation of pure crystalline CeO(2,) possessing a cubic fluorite structure with an average crystallite size of 15.6 to 16.4 nm. Electron microscopy studies reveal the formation of cube-shaped CeO(2) nanostructures with sizes below 25 nm. The cube-shaped CeO(2) nanostructures exhibited a higher BET surface area compared to their bulk counterparts. The XPS analysis has confirmed the existence of Ce in the mixed oxidation states of +3 and +4, while O is present as O(2–) in the sample. The as-synthesized CeO(2) nanostructures exhibit excellent catalytic activity in both the ipso-hydroxylation of aryl boronic acids and the aza-Michael reaction. The analysis of the used catalyst has confirmed its stability under the reported reaction conditions. The catalysts retain their catalytic activity up to the fifth run in both types of reactions, which is economically beneficial for industrial application. |
format | Online Article Text |
id | pubmed-9685755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96857552022-11-25 Template-Less and Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic Application in Ipso-hydroxylation of Aryl Boronic Acids and the aza-Michael Reaction Chandra Saikia, Tulan Borgohain, Xavy Iraqui, Saddam Rashid, Md. Harunar ACS Omega [Image: see text] Due to its excellent physicochemical properties, CeO(2) has found great importance as an electrochemical and in electronics, photocatalysis, sensing, and heterogeneous catalysis. Herein, we report the surfactant-less and template-less synthesis of CeO(2) nanostructures by the hydrothermal method. The synthesized CeO(2) nanostructures have been characterized in detail by electron microscopy, spectroscopy, diffractometry, and other analytical methods. The XRD studies revealed the formation of pure crystalline CeO(2,) possessing a cubic fluorite structure with an average crystallite size of 15.6 to 16.4 nm. Electron microscopy studies reveal the formation of cube-shaped CeO(2) nanostructures with sizes below 25 nm. The cube-shaped CeO(2) nanostructures exhibited a higher BET surface area compared to their bulk counterparts. The XPS analysis has confirmed the existence of Ce in the mixed oxidation states of +3 and +4, while O is present as O(2–) in the sample. The as-synthesized CeO(2) nanostructures exhibit excellent catalytic activity in both the ipso-hydroxylation of aryl boronic acids and the aza-Michael reaction. The analysis of the used catalyst has confirmed its stability under the reported reaction conditions. The catalysts retain their catalytic activity up to the fifth run in both types of reactions, which is economically beneficial for industrial application. American Chemical Society 2022-11-11 /pmc/articles/PMC9685755/ /pubmed/36440121 http://dx.doi.org/10.1021/acsomega.2c04614 Text en © 2022 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 | Chandra Saikia, Tulan Borgohain, Xavy Iraqui, Saddam Rashid, Md. Harunar Template-Less and Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic Application in Ipso-hydroxylation of Aryl Boronic Acids and the aza-Michael Reaction |
title | Template-Less and
Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic
Application in Ipso-hydroxylation of Aryl Boronic
Acids and the aza-Michael Reaction |
title_full | Template-Less and
Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic
Application in Ipso-hydroxylation of Aryl Boronic
Acids and the aza-Michael Reaction |
title_fullStr | Template-Less and
Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic
Application in Ipso-hydroxylation of Aryl Boronic
Acids and the aza-Michael Reaction |
title_full_unstemmed | Template-Less and
Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic
Application in Ipso-hydroxylation of Aryl Boronic
Acids and the aza-Michael Reaction |
title_short | Template-Less and
Surfactant-Less Synthesis of CeO(2) Nanostructures for Catalytic
Application in Ipso-hydroxylation of Aryl Boronic
Acids and the aza-Michael Reaction |
title_sort | template-less and
surfactant-less synthesis of ceo(2) nanostructures for catalytic
application in ipso-hydroxylation of aryl boronic
acids and the aza-michael reaction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685755/ https://www.ncbi.nlm.nih.gov/pubmed/36440121 http://dx.doi.org/10.1021/acsomega.2c04614 |
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