Issue 18, 2005

Cyclen based bis-macrocyclic ligands as phosphates receptors. A potentiometric and NMR study

Abstract

The host–guest interaction between orthophosphate, pyrophosphate and triphosphate anions and four cyclen based bis-macrocycles ligands possessing ortho-(BOC), meta-(BMC), para-xylenyl (BPC) or 2,6-pyridinyl (BPyC) linker was investigated by potentiometric measurements and NMR spectroscopy. Each ligand gave protonated species in aqueous solution that further formed ternary complexes after binding with anions; these complexes were analyzed as a result of hydrogen bond formation and Coulombic attraction between the organic host and the inorganic guest. The equilibrium constants for all the detected species are reported and the selectivity, illustrated with species distribution diagrams, is discussed. The results unambiguously showed the importance of the distance between the two cyclen cores and underlined, especially for the triphosphate species, the contribution of the nitrogen atom of the pyridinyl spacer as a supplementary anchoring point in acidic medium.

Graphical abstract: Cyclen based bis-macrocyclic ligands as phosphates receptors. A potentiometric and NMR study

Supplementary files

Article information

Article type
Paper
Submitted
14 Jun 2005
Accepted
12 Jul 2005
First published
11 Aug 2005

Dalton Trans., 2005, 3016-3024

Cyclen based bis-macrocyclic ligands as phosphates receptors. A potentiometric and NMR study

S. Develay, R. Tripier, M. Le Baccon, V. Patinec, G. Serratrice and H. Handel, Dalton Trans., 2005, 3016 DOI: 10.1039/B507819A

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