The
rapid detection and differentiation of chiral compounds is
important to synthetic, medicinal, and biological chemistry. Palladium
complexes with chiral pincer ligands are demonstrated to have utility
in determining the chirality of various amines. The binding of enantiomeric
amines induces distinct <sup>19</sup>F NMR shifts of the fluorine
atoms appended on the ligand that defines a chiral environment around
palladium. It is further demonstrated that this method has the ability
to evaluate the enantiomeric composition and discriminate between
enantiomers with chiral centers several carbons away from the binding
site. The wide detection window provided by optimized chiral chemosensors
allows the simultaneous identification of as many as 12 chiral amines.
The extraordinary discriminating ability of this method is demonstrated
by the resolution of chiral aliphatic amines that are difficult to
separate using chiral chromatography