4.5 Article

Anion Recognition by Neutral Macrocyclic Azole Amides

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2009, 期 2, 页码 213-222

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200800811

关键词

Anions; Host-guest systems; Hydrogen bonds; Macrocyclic ligands; Receptors

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A straightforward synthesis of C-2-symmetric azole-containing macrocyclic peptides is presented. This type of macrocycle possesses four amide groups directed into the interior of the scaffold that act as hydrogen-bond donors and two nitrogen atoms from the azole unit that act as hydrogen-bond acceptors. This arrangement makes them sensitive receptors for Y-shaped anions like AcO- and H2PO4- with a selectivity for dibydrogen phosphate versus acetate, as was shown with H-1 NMR titration techniques in [D-6]DMSO/5% CDCl3. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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