Adamantanes as spherical nanosondes in adducts with a chiral dirhodium complex-discriminating enantiomers and probing spatial proximities.

Three different kinds of substituted chiral adamantane molecules-adamantanones, dioxolanoadamantanes and dithiolano-adamantanes-were studied in the dirhodium experiment (NMR measurement with 1:1 molar mixtures with Rh((II))(2)[(R)-(+)-MTPA](4) in CDCl(3)). Their different behavior in adduct formation is described, and the possibility of determining enantiomeric purities and absolute configurations is explored. Detailed inspection of one- and two-dimensional NMR experiments allowed for an interpretation of steric and electronic intra-adduct interaction showing that the phenyl groups of Rh* tend to enwrap the bound adamantane ligand so that through-space effects over a range of 6-7 Å away from the binding rhodium atom can be observed. Even slight differences in the relative orientation of phenyl groups can be monitored when comparing diastereomeric adducts via NMR signal dispersion.