Abstract

The stability constants of the mixed-ligand complexes formed between Cu(Arm) 2+, where Arm = 2,2′-bipyridine (Bpy) or 1,10-phenanthroline (Phen), and the dianions of 9-[2-(2-phosphonoethoxy)ethyl]adenine (PEEA 2−) and (2-phosphonoethoxy)ethane (PEE 2−), also known as [2-(2-ethoxy)ethyl]phosphonate, were determined by potentiometric pH titrations in aqueous solution (25 °C; I = 0.1 M, NaNO 3). The ternary Cu(Arm)(PEEA) complexes are considerably more stable than the corresponding Cu(Arm)(R-PO 3) species, where R - PO 3 2 - represents a phosph(on)ate ligand with a group R that is unable to participate in any kind of interaction within the complexes. The increased stability is attributed to intramolecular stack formation in the Cu(Arm)(PEEA) complexes and also, to a smaller extent, to the formation of 6-membered chelates involving the ether oxygen atom present in the CH 2 O CH 2 CH 2 PO 3 2 - residue of PEEA 2−. This latter interaction is separately quantified by studying the ternary Cu(Arm)(PEE) complexes which can form the 6-membered chelates but where no intramolecular ligand–ligand stacking is possible. Application of these results allows a quantitative analysis of the intramolecular equilibria involving three structurally different Cu(Arm)(PEEA) species; e.g., of the Cu(Bpy)(PEEA) system about 11% exist with the metal ion solely coordinated to the phosphonate group, 4% as a 6-membered chelate involving the ether oxygen atom of the CH 2 O CH 2 CH 2 PO 3 2 - residue, and 85% with an intramolecular stack between the adenine moiety of PEEA 2− and the aromatic rings of Bpy. In addition, the Cu(Arm)(PEEA) complexes may be protonated, leading to Cu(Arm)(H;PEEA) + species for which it is concluded that the proton is located at the phosphonate group and that the complexes are mainly formed (50 and 70%) by a stacking adduct between Cu(Arm) 2+ and the adenine residue of H(PEEA) −. Finally, the stacking properties of adenosine 5′-monophosphate (AMP 2−), of the dianion of 9-[2-(phophonomethoxy)ethyl]adenine (PMEA 2−) and of several of its analogues (=PA 2−) are compared in their ternary Cu(Arm)(AMP) and Cu(Arm)(PA) systems. Conclusions regarding the antiviral properties of several acyclic nucleoside phosphonates are shortly discussed.

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