This communication describes preliminary results of an experimental investi
gation of the binding of Cu(II) ions to poly(amidoamine) (PAMAM) dendrimers
in aqueous solutions. Dendrimers are highly branched polymers with control
led composition and architecture consisting of three structural components:
a core, interior branch cells, and terminal branch cells. PAMAM dendrimers
possess functional nitrogen and amide groups arranged in regular "branched
upon branched" patterns which are displayed in geometrically progressive n
umbers as a function of generation level. Terminal groups of PAMAM dendrime
rs may be any organic substituent such as primary amines, carboxylic groups
, etc. In aqueous solutions, PAMAM dendrimers can serve as high capacity na
noscale containers for toxic metal ions such as Cu(II). Compared to traditi
onal chelating agents (e.g., triethylene tetramine) and macrocyles (e.g., c
yclams) with nitrogen donors, which can typically bind only one Cu(II) ion
per molecule, a generation eight (G8) PAMAM dendrimer can bind up 153 +/- 2
0 Cu(II) ions per molecule. This clearly illustrates a distinct advantage o
f dendrimers over traditional chelating agents and macrocycles; that is the
covalent attachment of nitrogen ligands to conformationally flexible PAMAM
chains enclosed within a nanoscopic structure results in a substantial inc
rease in binding capacity.