“…Further investigations on solid salts of U^(P2Wi706i)2'®" [2] and EU^CASJWI^OSOJ"" [3] complexes have shown that the coordination environment of U"^ and Eu'"^ in these Compounds, imposed by the two ligand groups (eight oxygen fonning a D4<, Square "Archimede's" antiprism), can explain the complexation of the "f" cations. Due to their highest charge density, complexes with M^^ ions such as Ce^^ [8], [1], Np^^ [7], Pu-'^ [1] or Am''^ [4] are considerably stronger than complexes with M"^ ions, such as Ce^^ [8], Nd'"^ [9] or Am^^ [5,7].…”