Copper(II) azacyclam complexes were obtained through a metal-templated procedure involving the pertinent open-chain tetramine, formaldehyde and a phenylurea derivative as a locking fragment. Both metal complexes can establish interactions with anions through the metal centre and the amide NH group. Equilibrium studies in DMSO by a spectrophotometric titration technique were carried out to assess the affinity of the complexes towards anions. While the NH group of an amide model compound and the metal centre of the plain CuII(azacyclam)2+ complex do not interact at all with anions, the new complexes establish strong interactions with oxo anions, profiting from a pronounced cooperative effect. In particular, 1) they form stable 1:1 and 1:2 complexes with H2PO4- ions in a stepwise mode with both hydrogen-bonding and metal–ligand interactions, and 2) in the presence of CH3COO-, they undergo deprotonation of the amido NH group and thus profit from axial coordination of the partially negatively charged carbonyl oxygen atom in a scorpionate binding mode.
Templated Synthesis of Copper(II) Azacyclam Complexes Using Urea as a Locking Fragment and Their Metal-Enhanced Binding Tendencies towards Anions
BOIOCCHI, MASSIMO;FABBRIZZI, LUIGI;LICCHELLI, MAURIZIO;MOSCA, LORENZO;ZANINI, CRISTINA
2009-01-01
Abstract
Copper(II) azacyclam complexes were obtained through a metal-templated procedure involving the pertinent open-chain tetramine, formaldehyde and a phenylurea derivative as a locking fragment. Both metal complexes can establish interactions with anions through the metal centre and the amide NH group. Equilibrium studies in DMSO by a spectrophotometric titration technique were carried out to assess the affinity of the complexes towards anions. While the NH group of an amide model compound and the metal centre of the plain CuII(azacyclam)2+ complex do not interact at all with anions, the new complexes establish strong interactions with oxo anions, profiting from a pronounced cooperative effect. In particular, 1) they form stable 1:1 and 1:2 complexes with H2PO4- ions in a stepwise mode with both hydrogen-bonding and metal–ligand interactions, and 2) in the presence of CH3COO-, they undergo deprotonation of the amido NH group and thus profit from axial coordination of the partially negatively charged carbonyl oxygen atom in a scorpionate binding mode.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
