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Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions
The synthesis of a Co metal–organic framework assembled from 5,10,15,20-tetrakis((pyridin-4-yl)phenyl)porphyrin; TPhPyP) “Co-MTPhPyP” is reported. The TPhPyP ligand was synthesized via aldehyde condensation in 28% yield and characterized by (1)H nuclear magnetic resonance ((1)H NMR), Fourier-transfo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964701/ https://www.ncbi.nlm.nih.gov/pubmed/36838804 http://dx.doi.org/10.3390/molecules28041816 |
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author | Arceo-Ruiz, Henry Xochitiotzi-Flores, Elba García-Ortega, Héctor Farfán, Norberto Santillan, Rosa Rincón, Susana Zepeda, Alejandro |
author_facet | Arceo-Ruiz, Henry Xochitiotzi-Flores, Elba García-Ortega, Héctor Farfán, Norberto Santillan, Rosa Rincón, Susana Zepeda, Alejandro |
author_sort | Arceo-Ruiz, Henry |
collection | PubMed |
description | The synthesis of a Co metal–organic framework assembled from 5,10,15,20-tetrakis((pyridin-4-yl)phenyl)porphyrin; TPhPyP) “Co-MTPhPyP” is reported. The TPhPyP ligand was synthesized via aldehyde condensation in 28% yield and characterized by (1)H nuclear magnetic resonance ((1)H NMR), Fourier-transform infrared (FTIR), high-resolution mass spectrometry (HRMS), and UV-visible spectroscopy (UV-vis). Co-MTPhPyP was prepared by the solvothermal method from TPhPyP and CoCl(2)·H(2)O in 55% yield and characterized by X-ray powder diffraction (XRD), FTIR, thermogravimetric analysis (TGA), field-emission scanning electron microscopy with energy-dispersive X-ray (FESEM-EDS), X-ray photoelectron spectroscopy (XPS), and dynamic light scattering (DLS), showing a particle size distribution of 418 ± 58 nm. The sorption properties of the Co-MTPhPyP for the effective removal of Pb(II) and Cu(II) were evaluated in an aqueous medium and Cthe results showed uptake capacities of 383.4 and 168 mg of the metal g(−1) after 2 h, respectively. Kinetic studies of Pb(II) adsorption by Co-MTPhPyP were adjusted to the pseudo-second-order model with a maximum adsorption capacity of 458.8 mg g(−1) at 30 min of exposition. |
format | Online Article Text |
id | pubmed-9964701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99647012023-02-26 Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions Arceo-Ruiz, Henry Xochitiotzi-Flores, Elba García-Ortega, Héctor Farfán, Norberto Santillan, Rosa Rincón, Susana Zepeda, Alejandro Molecules Article The synthesis of a Co metal–organic framework assembled from 5,10,15,20-tetrakis((pyridin-4-yl)phenyl)porphyrin; TPhPyP) “Co-MTPhPyP” is reported. The TPhPyP ligand was synthesized via aldehyde condensation in 28% yield and characterized by (1)H nuclear magnetic resonance ((1)H NMR), Fourier-transform infrared (FTIR), high-resolution mass spectrometry (HRMS), and UV-visible spectroscopy (UV-vis). Co-MTPhPyP was prepared by the solvothermal method from TPhPyP and CoCl(2)·H(2)O in 55% yield and characterized by X-ray powder diffraction (XRD), FTIR, thermogravimetric analysis (TGA), field-emission scanning electron microscopy with energy-dispersive X-ray (FESEM-EDS), X-ray photoelectron spectroscopy (XPS), and dynamic light scattering (DLS), showing a particle size distribution of 418 ± 58 nm. The sorption properties of the Co-MTPhPyP for the effective removal of Pb(II) and Cu(II) were evaluated in an aqueous medium and Cthe results showed uptake capacities of 383.4 and 168 mg of the metal g(−1) after 2 h, respectively. Kinetic studies of Pb(II) adsorption by Co-MTPhPyP were adjusted to the pseudo-second-order model with a maximum adsorption capacity of 458.8 mg g(−1) at 30 min of exposition. MDPI 2023-02-15 /pmc/articles/PMC9964701/ /pubmed/36838804 http://dx.doi.org/10.3390/molecules28041816 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Arceo-Ruiz, Henry Xochitiotzi-Flores, Elba García-Ortega, Héctor Farfán, Norberto Santillan, Rosa Rincón, Susana Zepeda, Alejandro Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions |
title | Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions |
title_full | Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions |
title_fullStr | Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions |
title_full_unstemmed | Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions |
title_short | Synthesis of a New Co Metal–Organic Framework Assembled from 5,10,15,20-Tetrakis((pyridin-4-yl) phenyl)porphyrin “Co-MTPhPyP” and Its Application to the Removal of Heavy Metal Ions |
title_sort | synthesis of a new co metal–organic framework assembled from 5,10,15,20-tetrakis((pyridin-4-yl) phenyl)porphyrin “co-mtphpyp” and its application to the removal of heavy metal ions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9964701/ https://www.ncbi.nlm.nih.gov/pubmed/36838804 http://dx.doi.org/10.3390/molecules28041816 |
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