A new class of tetraamidic selectors with arms derived from L-phenylal
anine and spaced by a phenolic template was synthesized. These chiral
compounds were used as stationary phases for analytical gas chromatogr
aphic resolution of racemic mixtures of volatile amino acid derivative
s; H-1 NMR titration experiments were also performed. The experimental
gas chromatographic and H-1 NMR data collected support the hypothesis
of a cooperation of the two chiral arms in binding and recognition of
amino acidic substrates. (C) 1998 Elsevier Science B.V.