P. Hayoz et al., STEREOSELECTIVE SYNTHESIS OF OCTAHEDRAL COMPLEXES WITH PREDETERMINED HELICAL CHIRALITY, Journal of the American Chemical Society, 115(12), 1993, pp. 5111-5114
Facile stereoselective synthesis of an enantiomerically pure DELTA-Ru-
trisbipyridine type complex is accomplished by using a new chiral and
conformationally rigid ligand, which completely predetermines the heli
cal chirality of the metal, yielding exclusively DELTA-configuration i
n the present case. The ligand, abbreviated chiragen[6] is a bisbipyri
dine compound, where two pinene substituted bipyridine units are linke
d through an aliphatic C6-chain. The two remaining coordination sites
of the complex are occupied by 4,4'-dimethylbipyridine. The structure
of the u(chiragen-[6])(4,4'-dimethylbipyridine)](CF3SO3)2 complex has
been determined by X-ray crystallography. Metal complexes formed by ch
iragen ligands have potential applications in enantioselective catalys
is and as chiral building blocks for polynuclear species.