The purpose of this review is to highlight new ligands that have been
immobilized on polymers to form polymer-supported reagents which are s
elective for the complexation of targeted metal ions from multicompone
nt solutions. Polystyrene remains the most popular organic polymer sup
port, and its synthesis by suspension polymerization yields beads with
a diameter appropriate for large-scale applications. Immobilized liga
nds include amines, pyridines, imidazoles, oximes, hydroxylamines, Sch
iff bases, thiols, crown ethers, and a varity of phosphorus ligands. T
he concepts inherent to reactive ion exchange, as first described by H
elfferich, and the recently synthesized dual mechanism bifunctional po
lymers can be used to build a unified theory of selectivity with polym
er-supported reagents. The goal remains to engineer selectivity into p
olymeric reagents in an a priori manner by understanding the basic pri
nciples through which a polymeric reagent can recognize a targeted sub
strate.