Background
Type: Article

Synthesis of tris-(azacrown) ethers for carboxylic acid recognition

Journal: Tetrahedron (14645416)Year: 7 January 2013Volume: 69Issue: Pages: 38 - 42
Lee, MichaelZali Boeini H.aLi, FengLindoy, Leonard F.Jolliffe, Katrina A.
DOI:10.1016/j.tet.2012.10.067Language: English

Abstract

The synergistic enhancement of metal ion extraction by azacrown ethers in the presence of carboxylic acids has been attributed to a ligand assembly effect in which these two ligands form a complex, facilitated by proton transfer, prior to complexation of the metal ion. In order to investigate the first steps in this multi-component complexation procedure, six tris-(azacrown) ethers were synthesised in high yields and their ability to complex mono- and tri-carboxylic acids was investigated by 1H NMR in methanol-d4. All six compounds bound to benzoic acid with 1:3 host-guest stoichiometry and four of them bound tricarboxylic acids with 1:1 host-guest stoichiometry, providing good support for the proposed first step in the ligand assembly effect. © 2012 Elsevier Ltd. All rights reserved.