Issue 20, 2004
From the journal:

Organic & Biomolecular Chemistry

Anion binding properties of 5,5′-dicarboxamido-dipyrrolylmethanes†

Ismael El Drubi Vega,a   Philip A. Gale,*a   Michael B. Hursthousea  and  Mark E. Lighta  

* Corresponding authors

a School of Chemistry, University of Southampton, Southampton, UK
E-mail: philip.gale@soton.ac.uk
Fax: +44 (0) 23 80596805
Tel: +44 (0)23 80593332

Abstract

A series of 5,5′-dicarboxamido-dipyrrolylmethanes have been synthesized and in some cases crystallographically characterized. Proton NMR titrations have revealed that these compounds, that contain only four neutral hydrogen bond donors and are acyclic, selectively bind anions in very competitive solvent media such as DMSO-d6/water mixtures.

Graphical abstract: Anion binding properties of 5,5′-dicarboxamido-dipyrrolylmethanes

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Article information

DOI
https://doi.org/10.1039/B409115A
Article type
Paper
Submitted
15 Jun 2004
Accepted
10 Aug 2004
First published
14 Sep 2004

Org. Biomol. Chem., 2004,2, 2935-2941

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Anion binding properties of 5,5′-dicarboxamido-dipyrrolylmethanes

I. El Drubi Vega, P. A. Gale, M. B. Hursthouse and M. E. Light, Org. Biomol. Chem., 2004, 2, 2935 DOI: 10.1039/B409115A

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