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Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives
In the current paper, we produce a new metal–organic framework (MOF) based on Zr metal, [Zr-UiO-66-PDC-SO(3)H]FeCl(4), via an anion exchange method, which is fully characterized by FT-IR, SEM with elemental mapping and EDX, FE-SEM and TEM. Furthermore, the use of [Zr-UiO-66-PDC-SO(3)H]FeCl(4) as a p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985156/ https://www.ncbi.nlm.nih.gov/pubmed/35424891 http://dx.doi.org/10.1039/d1ra08710j |
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author | Jalili, Fatemeh Zarei, Mahmoud Zolfigol, Mohammad Ali Khazaei, Ardeshir |
author_facet | Jalili, Fatemeh Zarei, Mahmoud Zolfigol, Mohammad Ali Khazaei, Ardeshir |
author_sort | Jalili, Fatemeh |
collection | PubMed |
description | In the current paper, we produce a new metal–organic framework (MOF) based on Zr metal, [Zr-UiO-66-PDC-SO(3)H]FeCl(4), via an anion exchange method, which is fully characterized by FT-IR, SEM with elemental mapping and EDX, FE-SEM and TEM. Furthermore, the use of [Zr-UiO-66-PDC-SO(3)H]FeCl(4) as a porous catalyst was examined for the one-pot synthesis of novel dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives by reaction of 6-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione, 2-hydroxynaphthalene-1,4-dione and various aldehydes at 100 °C with good to excellent yields. |
format | Online Article Text |
id | pubmed-8985156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-89851562022-04-13 Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives Jalili, Fatemeh Zarei, Mahmoud Zolfigol, Mohammad Ali Khazaei, Ardeshir RSC Adv Chemistry In the current paper, we produce a new metal–organic framework (MOF) based on Zr metal, [Zr-UiO-66-PDC-SO(3)H]FeCl(4), via an anion exchange method, which is fully characterized by FT-IR, SEM with elemental mapping and EDX, FE-SEM and TEM. Furthermore, the use of [Zr-UiO-66-PDC-SO(3)H]FeCl(4) as a porous catalyst was examined for the one-pot synthesis of novel dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives by reaction of 6-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione, 2-hydroxynaphthalene-1,4-dione and various aldehydes at 100 °C with good to excellent yields. The Royal Society of Chemistry 2022-03-23 /pmc/articles/PMC8985156/ /pubmed/35424891 http://dx.doi.org/10.1039/d1ra08710j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Jalili, Fatemeh Zarei, Mahmoud Zolfigol, Mohammad Ali Khazaei, Ardeshir Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives |
title | Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives |
title_full | Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives |
title_fullStr | Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives |
title_full_unstemmed | Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives |
title_short | Application of novel metal–organic framework [Zr-UiO-66-PDC-SO(3)H]FeCl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives |
title_sort | application of novel metal–organic framework [zr-uio-66-pdc-so(3)h]fecl(4) in the synthesis of dihydrobenzo[g]pyrimido[4,5-b]quinoline derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985156/ https://www.ncbi.nlm.nih.gov/pubmed/35424891 http://dx.doi.org/10.1039/d1ra08710j |
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