Amphiphilic block copolymers self-assemble into a variety of mesoscopi
c structures comprising micellar and ordered continuous topologies. Si
ze and topology of these structures can be controlled by variation of
block lengths. Their stability allows the preparation of well-defined
polymer/inorganic hybrid materials. Quantum-size semiconductor colloid
s as well as nanometer-sized noble metal colloids can be prepared with
in block copolymer microdomains. Enhanced stability of such colloids a
llows to use them as efficient catalysts.