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Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar and Artificial Irradiation
[Image: see text] Two coordination polymers CP1 {[Zn(II)(BIPY)(Pht)](n)} and CP2 {[Zn(HYD)(Pht)](n)} (BIPY = 4,4′-bipyridine, Pht = terephthalic acid, and HYD = 8-hydroxyquinoline) have been successfully synthesized by a hydrothermal process using zinc aqueous solution. The so-prepared compounds wer...
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/PMC8945138/ https://www.ncbi.nlm.nih.gov/pubmed/35350348 http://dx.doi.org/10.1021/acsomega.1c06049 |
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author | Adala, Amina Debbache, Nadra Sehili, Tahar |
author_facet | Adala, Amina Debbache, Nadra Sehili, Tahar |
author_sort | Adala, Amina |
collection | PubMed |
description | [Image: see text] Two coordination polymers CP1 {[Zn(II)(BIPY)(Pht)](n)} and CP2 {[Zn(HYD)(Pht)](n)} (BIPY = 4,4′-bipyridine, Pht = terephthalic acid, and HYD = 8-hydroxyquinoline) have been successfully synthesized by a hydrothermal process using zinc aqueous solution. The so-prepared compounds were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, UV–visible spectroscopy, thermogravimetric analysis (TGA), and cyclic voltammetry. XRD pointed to a crystalline phase for CP1, while CP2 required recrystallization, FTIR spectroscopy established the presence of characteristic bands for all the ligands, and TGA showed thermal stability up to 100 °C. The electrochemical study showed a good charge transfer between the ligands and Zn metal for both materials. The UV–vis spectra displayed a strong absorption band spreading over a wide wavelength range, encompassing UV and visible light, with a band gap of 2.69 eV for CP1 and 2.56 eV for CP2, both of which are smaller than that of ZnO. This provides an advantageous alternative to using ZnO. The 5 × 10(–5) mol L(–1) ibuprofen decomposition kinetics under solar and UV light were studied under different irradiation conditions. Good photocatalytic properties were observed due to their high surface area. |
format | Online Article Text |
id | pubmed-8945138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89451382022-03-28 Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar and Artificial Irradiation Adala, Amina Debbache, Nadra Sehili, Tahar ACS Omega [Image: see text] Two coordination polymers CP1 {[Zn(II)(BIPY)(Pht)](n)} and CP2 {[Zn(HYD)(Pht)](n)} (BIPY = 4,4′-bipyridine, Pht = terephthalic acid, and HYD = 8-hydroxyquinoline) have been successfully synthesized by a hydrothermal process using zinc aqueous solution. The so-prepared compounds were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, UV–visible spectroscopy, thermogravimetric analysis (TGA), and cyclic voltammetry. XRD pointed to a crystalline phase for CP1, while CP2 required recrystallization, FTIR spectroscopy established the presence of characteristic bands for all the ligands, and TGA showed thermal stability up to 100 °C. The electrochemical study showed a good charge transfer between the ligands and Zn metal for both materials. The UV–vis spectra displayed a strong absorption band spreading over a wide wavelength range, encompassing UV and visible light, with a band gap of 2.69 eV for CP1 and 2.56 eV for CP2, both of which are smaller than that of ZnO. This provides an advantageous alternative to using ZnO. The 5 × 10(–5) mol L(–1) ibuprofen decomposition kinetics under solar and UV light were studied under different irradiation conditions. Good photocatalytic properties were observed due to their high surface area. American Chemical Society 2022-03-14 /pmc/articles/PMC8945138/ /pubmed/35350348 http://dx.doi.org/10.1021/acsomega.1c06049 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 | Adala, Amina Debbache, Nadra Sehili, Tahar Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar and Artificial Irradiation |
title | Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for
Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar
and Artificial Irradiation |
title_full | Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for
Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar
and Artificial Irradiation |
title_fullStr | Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for
Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar
and Artificial Irradiation |
title_full_unstemmed | Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for
Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar
and Artificial Irradiation |
title_short | Two Coordination Polymers Synthesized from Various N-Donor Clusters Spaced by Terephthalic Acid for
Efficient Photocatalytic Degradation of Ibuprofen in Water under Solar
and Artificial Irradiation |
title_sort | two coordination polymers synthesized from various n-donor clusters spaced by terephthalic acid for
efficient photocatalytic degradation of ibuprofen in water under solar
and artificial irradiation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945138/ https://www.ncbi.nlm.nih.gov/pubmed/35350348 http://dx.doi.org/10.1021/acsomega.1c06049 |
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