Journal
NEW JOURNAL OF CHEMISTRY
Volume 31, Issue 5, Pages 646-654Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b615673h
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A series of novel, acyclic pyrrole-based anion receptors is described that bind nitrite and carboxylate anions with good selectivity in dichloroethane solution. These systems, which are based on pyridine 2,6-dicarboxamides, also bind cyanide anions weakly. Control systems, incorporating a benzene-1,3-dicarboxamide spacer or wherein the connectivity of the amide linkage is reversed'', either failed to act as effective anion receptors or displayed very different selectivities.
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