An amphiphilic poly(acrylic acid)/polystyrene graft copolymer (PAA-g-P
S) has been used to form ''nanoreactors'' for the synthesis of gold cl
usters. Such copolymers tend to form stable micelles in non-polar orga
nic solvents where the poly(acrylic acid) chains constitute the core,
and the polystyrene chains, the shell. In the present study, the micel
lar structure of PAA-g-PS in toluene has been demonstrated by dynamic
light scattering and transmission electron microscopy (TEM). The subse
quent preparation of gold-graft copolymer composites involved the intr
oduction of gold chloride (AuCl3), either in powder form or previously
dissolved in ether, into the micellar cores of the PAA-g-PS in toluen
e. The gold salt was then reduced by ultraviolet (UV) irradiation of t
he emulsion, or of dried cast films. TEM and ultraviolet-visible (UV/V
is) spectroscopy were used to characterize the resulting composites. G
old particles of less than 5 nm in diameter were observed in all cases
, but the size distribution and the spatial arrangement of the cluster
s in the cast films were modified when diethyl ether was used to intro
duce AuCl3 into the PAA-g-PS micellar cores. This was thought to be du
e to enhanced nucleation of the gold particles and partial disruption
of the micellar cores in the presence of diethyl ether.