The first enantiomerically pure helical noncovalent tripod for assembling nine-coordinate lanthanide(III) podates

Decomplexation of the trivalent lanthanide, Ln(III), from the racemic bimetallic triple-stranded helicates LnCr(L8)(3)](6+) provides the inert chiral tripodal nonadentate receptor Cr(L8)(3)](3+). Elution of the latter podand with Na(2)Sb(2)(+)-C(4)O(6)H(2)](2).5H(2)O through a cation exchange column allows its separation into its inert helical enantiomers M-(+)(589)-Cr(L8)(3)](3+) and P-(-)(589)-Cr(L8)(3)](3+), whose absolute configurations are assigned by using CD spectroscopy and exciton theory. Recombination with Ln(III) restores the original triple-stranded helicates LnCr(L8)(3)](6+), and the associated thermodynamic parameters unravel the contribution of electrostatic repulsion and preorganization to the complexation process. Combining M-(+)(589)-Cr(L8)(3)](3+) with Eu(III) produces the enantiomerically pure d-f helicate MM-(-)(589)-EuCr(L8)(3)](CF(3)SO(3))(6).4CH(3)CN, whose X-ray crystal structure (EuCrC(113)H(111)N(25)O(21)S(6)F(18), monoclinic, P2(1), Z = 2) unambiguously confirms the absolute left-handed configuration for the final helix. The associated ligand-centered and metal-centered chiro-optical properties recorded for the complexes MM-LnCr(L8)(3)](6+) and PP-LnCr(L8)(3)](6+) (Ln = Eu, Gd, Tb) show a strong effect of helicity on specific rotary dispersions, CD and CPL spectra.