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Highly Active Cellulose-Supported Poly(hydroxamic acid)–Cu(II) Complex for Ullmann Etherification
[Image: see text] Highly active natural pandanus-extracted cellulose-supported poly(hydroxamic acid)–Cu(II) complex 4 was synthesized. The surface of pandanus cellulose was modified through graft copolymerization using purified methyl acrylate as a monomer. Then, copolymer methyl acrylate was conver...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970499/ https://www.ncbi.nlm.nih.gov/pubmed/33748590 http://dx.doi.org/10.1021/acsomega.0c05840 |
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author | Jian Fui, Choong Xin Ting, Tang Sarjadi, Mohd Sani Amin, Zarina Sarkar, Shaheen M. Musta, Baba Rahman, MdLutfor |
author_facet | Jian Fui, Choong Xin Ting, Tang Sarjadi, Mohd Sani Amin, Zarina Sarkar, Shaheen M. Musta, Baba Rahman, MdLutfor |
author_sort | Jian Fui, Choong |
collection | PubMed |
description | [Image: see text] Highly active natural pandanus-extracted cellulose-supported poly(hydroxamic acid)–Cu(II) complex 4 was synthesized. The surface of pandanus cellulose was modified through graft copolymerization using purified methyl acrylate as a monomer. Then, copolymer methyl acrylate was converted into a bidentate chelating ligand poly(hydroxamic acid) via a Loosen rearrangement in the presence of an aqueous solution of hydroxylamine. Finally, copper species were incorporated into poly(hydroxamic acid) via the adsorption process. Cu(II) complex 4 was fully characterized by Fourier transform infrared (FTIR), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray (EDX), transmission electron microscopy (TEM), inductively coupled plasma optical emission spectrometry (ICP-OES), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) analyses. The cellulose-supported Cu(II) complex 4 was successfully applied (0.005 mol %) to the Ullmann etherification of aryl, benzyl halides, and phenacyl bromide with a number of aromatic phenols to provide the corresponding ethers with excellent yield [benzyl halide (70–99%); aryl halide (20–90%)]. Cu(II) complex 4 showed high stability and was easily recovered from the reaction mixture. It could be reused up to seven times without loss of its original catalytic activity. Therefore, Cu(II) complex 4 can be commercially utilized for the preparation of various ethers, and this synthetic technique could be a part in the synthesis of natural products and medicinal compounds. |
format | Online Article Text |
id | pubmed-7970499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79704992021-03-19 Highly Active Cellulose-Supported Poly(hydroxamic acid)–Cu(II) Complex for Ullmann Etherification Jian Fui, Choong Xin Ting, Tang Sarjadi, Mohd Sani Amin, Zarina Sarkar, Shaheen M. Musta, Baba Rahman, MdLutfor ACS Omega [Image: see text] Highly active natural pandanus-extracted cellulose-supported poly(hydroxamic acid)–Cu(II) complex 4 was synthesized. The surface of pandanus cellulose was modified through graft copolymerization using purified methyl acrylate as a monomer. Then, copolymer methyl acrylate was converted into a bidentate chelating ligand poly(hydroxamic acid) via a Loosen rearrangement in the presence of an aqueous solution of hydroxylamine. Finally, copper species were incorporated into poly(hydroxamic acid) via the adsorption process. Cu(II) complex 4 was fully characterized by Fourier transform infrared (FTIR), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray (EDX), transmission electron microscopy (TEM), inductively coupled plasma optical emission spectrometry (ICP-OES), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) analyses. The cellulose-supported Cu(II) complex 4 was successfully applied (0.005 mol %) to the Ullmann etherification of aryl, benzyl halides, and phenacyl bromide with a number of aromatic phenols to provide the corresponding ethers with excellent yield [benzyl halide (70–99%); aryl halide (20–90%)]. Cu(II) complex 4 showed high stability and was easily recovered from the reaction mixture. It could be reused up to seven times without loss of its original catalytic activity. Therefore, Cu(II) complex 4 can be commercially utilized for the preparation of various ethers, and this synthetic technique could be a part in the synthesis of natural products and medicinal compounds. American Chemical Society 2021-03-05 /pmc/articles/PMC7970499/ /pubmed/33748590 http://dx.doi.org/10.1021/acsomega.0c05840 Text en © 2021 The Authors. Published by American Chemical Society 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 | Jian Fui, Choong Xin Ting, Tang Sarjadi, Mohd Sani Amin, Zarina Sarkar, Shaheen M. Musta, Baba Rahman, MdLutfor Highly Active Cellulose-Supported Poly(hydroxamic acid)–Cu(II) Complex for Ullmann Etherification |
title | Highly Active Cellulose-Supported Poly(hydroxamic
acid)–Cu(II) Complex for Ullmann Etherification |
title_full | Highly Active Cellulose-Supported Poly(hydroxamic
acid)–Cu(II) Complex for Ullmann Etherification |
title_fullStr | Highly Active Cellulose-Supported Poly(hydroxamic
acid)–Cu(II) Complex for Ullmann Etherification |
title_full_unstemmed | Highly Active Cellulose-Supported Poly(hydroxamic
acid)–Cu(II) Complex for Ullmann Etherification |
title_short | Highly Active Cellulose-Supported Poly(hydroxamic
acid)–Cu(II) Complex for Ullmann Etherification |
title_sort | highly active cellulose-supported poly(hydroxamic
acid)–cu(ii) complex for ullmann etherification |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970499/ https://www.ncbi.nlm.nih.gov/pubmed/33748590 http://dx.doi.org/10.1021/acsomega.0c05840 |
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