The ability to synthesise and tune photoresponsive and photoredox II-VI semi-conductor nanoparticles by quantum confinement is a continuously and rapidly developing area. Chemical methods are useful in producing dispersions of nanoparticles of uniform size in many organic solvents. Such synthetic methods employ the use of reverse micelles [1,2], phospholipid vesicles[3,4] or capping agents[5,6]to restrict particle size and growth to the nanometre regime.

The production of super lattice assemblies, through, for example the use of controlled crystallisation [7], Langmuir monolayers[8], Langmuir Blogget films[9], and self assembled short chain dithiol monolayers[10] on gold substrates has also received attention in the past. This latter approach potentially opens the way for self assembled electro-luminescent devices[11].

The ability to couple organic self assembly and inorganic nano-synthesis could also provide a route toward the chemical synthesis of an organised array of quantum-confined semiconductors. An aspect of this synthesis with construction approach is the possible coupling of biological templating systems to produce biomimetic materials [12,13]. In fact, an example would be the stabilised CdS nanoparticles in yeast binding to phytochelatin peptides which are secreted in response to metal toxicification [14].