Issue 7, 2016

Macrocyclic squaramides: anion receptors with high sulfate binding affinity and selectivity in aqueous media

Abstract

A number of macrocyclic squaramide-containing receptors (MSQs) have been designed and synthesised and their interaction with a range of inorganic anions was studied in solution by 1H NMR spectroscopy and ESI-HRMS. The binding data revealed remarkable binding of sulfate in aqueous mixtures from 0.5 to 50% v/v H2O/DMSO-d6. The larger [3]-MSQs were found to better match the size and shape of the sulfate ion than the [2]-MSQs, providing high affinity and selectivity for sulfate while other tetrahedral divalent anions such as selenate, phosphate species and chromate have substantially lower binding affinities. In mixtures of anions mimicking the composition of either nuclear waste or plasma, the [3]-MSQs were still able to bind sulfate ions with high affinity.

Graphical abstract: Macrocyclic squaramides: anion receptors with high sulfate binding affinity and selectivity in aqueous media

Supplementary files

Article information

Article type
Edge Article
Submitted
03 Mar 2016
Accepted
01 Apr 2016
First published
01 Apr 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2016,7, 4563-4572

Author version available

Macrocyclic squaramides: anion receptors with high sulfate binding affinity and selectivity in aqueous media

L. Qin, A. Hartley, P. Turner, R. B. P. Elmes and K. A. Jolliffe, Chem. Sci., 2016, 7, 4563 DOI: 10.1039/C6SC01011C

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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