Absolute stereochemistry of chiral C60 fullerene bis-adducts.

Abstract

To determine the absolute configuration of chiral fullerene bis-adducts, we have studied the double Bingel reaction of C60 with chiral tether (2S,3S)-(-)-9 derived from (R,R)-(+)-tartaric acid, and have succeeded in isolating two possible chiral bis-adducts 10a (5%) and 10b (2%) in addition to the Cs-symmetrically added derivative 10c (40%). The CD spectra of chiral bis-adducts [CD(+)281]-10a and [CD(-)281]-10b show very intense Cotton effects, which are almost of mirror image, indicating that their chiral C60 pi-electron systems are enantiomeric each other. The 1H and 13C NMR spectra of 10a and 10b indicate that they have C2-symmetrical structures, and the vicinal coupling constants between two equivalent protons H-2 and H-2' were determined as 1.2 Hz for 10a and 1.8 Hz for 10b, respectively by the 13C satellite band method. From the conformational analyses, the absolute configurations of these chiral C60 fullerene bis-adducts were unambiguously determined as [CD(+)281]-(S,S,fC)-10a and [CD(-)281]-(S,S,fA)-10b, respectively.