Linear polystyrene, having a trimethoxysilyl group at one side of the
terminal group, was newly synthesized and readily grafted onto porous
silica gels using the terminal reactive group. Its packed column showe
d good selectivity based on the pi-pi interaction for polyaromatics as
well as the usual reversed-phase mode separation for alkyl compounds.
The elution behavior (including the elution order) agreed with those
that were observed in non-silica-supported poly(styrene-divinylbenzene
) spherical particles. However, the asymmetric factor (A(s)) of the el
ution peaks for polyaromatics was much better in silica-supported poly
styrene than in non-supported polystyrene; for example, the values of
A(s) for triphenylene were 1.4 and 4.7, respectively. This difference
is attributable to the flexibility of the polystyrene chain.