A study on the coordinative versatility of new N,S-donor macrocyclic ligands: XAFS, and Cu2+ complexation thermodynamics in solution

• Published in: Dalton transactions : an international journal of inorganic chemistry Vol. 40; no. 12; pp. 2764 - 2777
• Main Authors: Aquilanti, Giuliana, Giorgetti, Marco, Minicucci, Marco, Papini, Grazia, Pellei, Maura, Tegoni, Matteo, Trasatti, Andrea, Santini, Carlo
• Format: Journal Article
• Language: English
• Published: England 01.01.2011
• Subjects: Bioagents; Complexation; Coordination Complexes - chemistry; Copper; Copper - chemistry; Copper compounds; Humans; Ligands; Macrocyclic compounds; Macrocyclic Compounds - chemistry; Nitrogen - chemistry; Protons; Serum Albumin - chemistry; Solid state; Solutions - chemistry; Stability; Sulfur - chemistry; Thermodynamics; X-Ray Absorption Spectroscopy
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/c0dt01401j

We investigated, both in the solid state and in aqueous solution, the coordination environment and stability behavior of four macrocyclic ligands (three N(2)S(2) and one N(3)S(2)) and of the corresponding Cu(II) complexes. The structural characterization in the solid state of the copper derivatives was performed by X-Ray Absorption Spectroscopy. Copper is found to be 4-fold coordinated with a CuN(2)S(2) environment with different Cu-S distances depending on the size of the macrocyclic ring. The EXAFS technique has indicated that nitrogen and sulfur atoms are more preferable to oxygen atoms as donor systems, without the evidence of coordination of the carboxylic moieties to copper in the first shell. The joint EXAFS and XANES study of the copper(II) complex with the N(3)S(2) ligand confirms the 4-fold coordination with an additional, long Cu-N interaction. The Cu(2+) complexation constants for one ligand were determined in aqueous solution. The results indicate that the species [CuL], although isolated in the solid state, is not the most abundant at the pH of blood serum. Instead, at pH 7.4 the protonated [Cu(HL)](+) species was found to be the most relevant. The behaviour of the copper complexes in the presence of the strong copper chelating bioagent human serum albumin was also examined in order to gain information on the stability of these compounds in biological fluids.