The reversed phase chromatographic properties of the [G1]-L-glutamic acid e
thyl ester-AC-silica (1), [G2]-L-glutamic acid ethyl ester-AC-silica (2) an
d the [G1]-L-glutamic acid t-butyl ester-AC-silica (3) dendrimer stationary
phases were evaluated. initial studies involved the comparison between the
se phases with a classic reversed phase (i.e. ODS1) by the separation of a
standard reversed phase test mixture composed of dimethylphthalate, nitrobe
nzene, anisole, diphenylamine and fluorene. Separations were achieved with
comparable performance to those obtained with the conventional reversed pha
se (ODS1). However, it was apparent that he chromatographic selectivity exh
ibited by the dendrimer stationary phases was different from that of the OD
S1 phase. On a per mole basis the dendrimers exhibited similar land sometim
es greater) affinity for these analytes compared with the ODS1 ligand. Subs
equent chromatographic experiments were conducted upon the dendrimer chiral
stationary phases using chiral analytes under reversed phase and normal ph
ase conditions. Chiral resolution was not observed.