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First use of p-tert-butylcalix[4]arene-tetra-O-acetate as a nanoreactor having tunable selectivity towards cross azo-compounds by trapping silver ions
p-tert-Butylcalix[4]arene-tetra-O-ac etate was established for the first time as a member of the nanoreactor series, even without having any -OH group. The nano range distribution of this nanoreactor was ascertained by DLS, SEM and TEM studies. The capability of this cavitand towards hosting amines...
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Published in: | Green chemistry : an international journal and green chemistry resource : GC 2016-01, Vol.18 (2), p.442-451 |
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container_title | Green chemistry : an international journal and green chemistry resource : GC |
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creator | Sarkar, Piyali Mukhopadhyay, Chhanda |
description | p-tert-Butylcalix[4]arene-tetra-O-ac etate was established for the first time as a member of the nanoreactor series, even without having any -OH group. The nano range distribution of this nanoreactor was ascertained by DLS, SEM and TEM studies. The capability of this cavitand towards hosting amines in a competitive manner generates a new green pathway for cross coupling of aromatic amines to give the corresponding azo-compounds. In this context, using p-tert-butylcalix[4]arene-tetra-O -acetate as a nanoreactor and silver nitrate as a catalyst, we got the cross azo-compound in good to excellent yields in the eco-friendly solvent water. This green methodology is also applicable for the synthesis of respective homo-compounds. |
doi_str_mv | 10.1039/c5gc01859e |
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Amines Cross coupling Nanostructure Pathways Silver nitrates Solvents Synthesis Trapping |
title | First use of p-tert-butylcalix[4]arene-tetra-O-acetate as a nanoreactor having tunable selectivity towards cross azo-compounds by trapping silver ions |
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