Metal ion recognition: the interaction of cobalt(II), nickel(II), copper(II), zinc(II), cadmium(II), silver(I) and lead(II) with N-benzylated macrocycles incorporating O2N2-, O3N2- and O2N3-donor sets

The interaction of cobalt(II), nickel(II), copper(II), zinc(II), cadmium(II), silver(I) and lead(II) with a series of mixed-donor, N-benzylated macrocyclic ligands incorporating O2N2-, O3N2- and O2N3-donor sets has been investigated. The log K values for the respective 1 1 complexes in 95% methanol (I= 0.1 mol dm–3; Et4NClO4, 25 °C) have been determined potentiometrically and the results compared with the values obtained previously for the parent (non-benzylated) macrocyclic systems. Examples of N-benzylation of individual parent macrocycles leading to enhanced discrimination for silver(I) are presented. In the case of a dibenzylated O3N2-ring and a tribenzylated O2N3-ring, both 17-membered, high selectivity for this ion was observed relative to the other metal ions investigated. Competitive mixed-metal transport experiments across a bulk chloroform membrane have been performed using the benzylated derivatives as ionophores. For each experiment the source contained equimolar concentrations of the above metal ions and transport was performed against a pH gradient; the aqueous source and receiving phases were buffered at pH 4.9 and 3.0, respectively. In parallel to the log K results, transport selectivity for silver(I) was exhibited by the di- and tri-benzylated ligands mentioned above. The remaining ligands proved to be poor ionophores, showing no significant metal ion transport under the conditions employed. In a further study, high silver ion (transport) selectivity was maintained when the above tribenzylated ligand was incorporated as the ionophore in a polymer inclusion membrane system. Single metal and mixed (seven-metal) solvent extraction experiments employing similar aqueous source and chloroform phases to those used in the bulk membrane transport runs have also been performed for the tribenzylated ligand derivative; significant selectivity for silver was again maintained in these solvent extraction experiments. An X-ray study of [AgL]ClO4(where L is the above-mentioned dibenzylated derivative) confirms that all donor atoms of the macrocycle coordinate to the silver ion; the latter is five-coordinate with the complex cation exhibiting a highly distorted trigonal bipyramidal geometry