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Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H

The purpose of this work is to develop a magnetically recyclable immobilized base catalyst for the green synthesis of calixresorcarenes. To achieve this, poly triazine-benzene sulfonamide (PTBSA) has been coated on magnetic Fe(3)O(4) nanoparticles and subsequently chlorosulfonic acid has been suppor...

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Autores principales: Gharehkhani, Alireza, Ghorbani-vaghei, Ramin, Alavinia, Sedigheh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043749/
https://www.ncbi.nlm.nih.gov/pubmed/35496418
http://dx.doi.org/10.1039/d1ra07393a
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author Gharehkhani, Alireza
Ghorbani-vaghei, Ramin
Alavinia, Sedigheh
author_facet Gharehkhani, Alireza
Ghorbani-vaghei, Ramin
Alavinia, Sedigheh
author_sort Gharehkhani, Alireza
collection PubMed
description The purpose of this work is to develop a magnetically recyclable immobilized base catalyst for the green synthesis of calixresorcarenes. To achieve this, poly triazine-benzene sulfonamide (PTBSA) has been coated on magnetic Fe(3)O(4) nanoparticles and subsequently chlorosulfonic acid has been supported to obtain Fe(3)O(4)@PTBSA-SO(3)H. The structure of nano-Fe(3)O(4)@PTBSA-SO(3)H was characterized by TEM, XRD, FT-IR, VSM, WDX, EDX, TGA/DSC and FE-SEM. The catalytic efficiency of this catalyst was also investigated in the synthesis of novel calixresorcarene derivatives. The advantages of heterogeneous nature, catalytic activity and the recyclability of the polymer support were also strengthened by advanced surface treatment. These key factors (basic sites, acidic sites and heterogeneity) play essential roles in the catalyst performance. This procedure has some advantages such as short reaction time, clean and fast work-up and easy separation of the catalyst by an external magnet.
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spelling pubmed-90437492022-04-28 Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H Gharehkhani, Alireza Ghorbani-vaghei, Ramin Alavinia, Sedigheh RSC Adv Chemistry The purpose of this work is to develop a magnetically recyclable immobilized base catalyst for the green synthesis of calixresorcarenes. To achieve this, poly triazine-benzene sulfonamide (PTBSA) has been coated on magnetic Fe(3)O(4) nanoparticles and subsequently chlorosulfonic acid has been supported to obtain Fe(3)O(4)@PTBSA-SO(3)H. The structure of nano-Fe(3)O(4)@PTBSA-SO(3)H was characterized by TEM, XRD, FT-IR, VSM, WDX, EDX, TGA/DSC and FE-SEM. The catalytic efficiency of this catalyst was also investigated in the synthesis of novel calixresorcarene derivatives. The advantages of heterogeneous nature, catalytic activity and the recyclability of the polymer support were also strengthened by advanced surface treatment. These key factors (basic sites, acidic sites and heterogeneity) play essential roles in the catalyst performance. This procedure has some advantages such as short reaction time, clean and fast work-up and easy separation of the catalyst by an external magnet. The Royal Society of Chemistry 2021-11-22 /pmc/articles/PMC9043749/ /pubmed/35496418 http://dx.doi.org/10.1039/d1ra07393a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Gharehkhani, Alireza
Ghorbani-vaghei, Ramin
Alavinia, Sedigheh
Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H
title Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H
title_full Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H
title_fullStr Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H
title_full_unstemmed Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H
title_short Synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-SO(3)H
title_sort synthesis of calixresorcarenes using magnetic poly triazine-benzene sulfonamide-so(3)h
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043749/
https://www.ncbi.nlm.nih.gov/pubmed/35496418
http://dx.doi.org/10.1039/d1ra07393a
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