Chain structure solution self-assembly

FIG. 1 Self-assembled structures in amphiphilic systems micellar structures (a) and (b) exist in aqueous solution as well as in ternary oil/water/amphiphile mixtures. In the latter case, they are swollen by the oil on the hydrophobic (tail) side. Monolayers (c) separate water from oil domains in ternary systems. Lipids in water tend to form bilayers (d) rather than micelles, since their hydrophobic block (two chains) is so compact and bulky, compared to the head group, that they cannot easily pack into a sphere [4]. At small concentrations, bilayers often close up to form vesicles (e). Some surfactants also form cyhndrical (wormlike) micelles (not shown). 

The examples discussed above illustrate the importance of block copolymer chain segment incompatibilities for the phase separation of bulk materials, combined with the ability to perform chemistry within specific nanoscale domains to impose permanence upon those self-assembled nanostructured morphologies. Each is limited, however, to crosslinking of internal domains within the solid-state assemblies in order to create discrete nanoscale objects. To advance the level of control over regioselective crosslinking and offer methodologies that allow for the production of additional unique nanostructured materials, the pre-assembled structures can be produced in solution (Figure 6.4), as isolated islands with reactivity allowed either internally or on the external... 

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