“…The copper(II) (À)-sparteine complexes are usually four-coordinate and tetrahedrally distorted around the approximately squareplanar copper(II) ion, as a result of the steric requirements imposed by the bulky chelating (À)-sparteine ligand (Choi et al, , 2004Kim et al, 2001Kim et al, , 2002Kim et al, , 2003Lee et al, 2000Lee et al, , 2003Lopez et al, 1998). The chiral diamine alkaloid, (À)sparteine, has three diastereomers, namely (À)-l-sparteine (C 15 H 26 N 2 ), (À)--isosparteine (-C 15 H 26 N 2 ) and (À)-isosparteine (-C 15 H 26 N 2 ), and has been utilized extensively in medicinal chemistry (Cady et al, 1977), in the asymmetric synthesis of chiral compounds (Beak et al, 1996) and in the preparation of a model compound of the type I copper(II) sites in copper proteins (Kim et al, 2001). Although fourcoordinate copper(II) compounds with (À)-l-sparteine, (À)--isosparteine and (À)--isosparteine have similar tetrahedrally distorted square-planar structures, the different conformations of three (À)-sparteine diastereomers in these compounds impose different degrees of steric effect on the geometry around the copper(II) centre.…”