Molecular routes to the formation of ordered inorganic arrays
Anisotropic inorganic materials are desirable as they possess unique physical and chemical properties resulting from the manner in which the particulate components assemble. The facility to control the ordering of colloidal inorganic particles could presage dramatic improvements in the fabrication of ceramics, catalysts or paints. Biological systems have already harnessed the manifold advantages of such materials, consider shells, teeth, bones etc.(Figures 1 & 2). Synthetic strategies for the formation of nanodimensional inorganic solids abound but there are few reliable methods currently available for directing their subsequent aggregation. Some degree of ordering can be achieved by the application of external forces (magnetic, electrical) but the aggregates readily dissemble once the stimulus is removed. The requirement is, therefore, for an effective molecular route to the ordered assembly and construction of hierarchical inorganic microstructures.The present work forms part of an extended programme of research investigating crystal tectonics, the ordering of nanodimensional inorganic solids. Here, the controlled morphological tailoring of inorganic crystals to yield a form which favours self-assembly has been investigated.