Liquid crystal templating as an approach to spatially and temporally organise soft matter.

Chemistry quickly moves from a molecular science to a systems science. This requires spatial and temporal control over the organisation of molecules and molecular assemblies. Whilst Nature almost by default (transiently) organises her components at multiple different length scales, scientists struggle to realise even relatively straightforward patterns.

Solid-Liquid Interface Structure of Muscovite Mica in CsCl and RbBr Solutions.

The solid-liquid interface formed by single terminated muscovite mica in contact with two different ionic solutions is analyzed using surface X-ray diffraction. Specular and nonspecular crystal truncation rods of freshly cleaved mica immersed in CsCl or RbBr aqueous solution were measured. The half monolayer of the surface potassium ions present after the cleavage is completely replaced by the positive ions (Cs or Rb) from the solution.

Directed peptide amphiphile assembly using aqueous liquid crystal templates in magnetic fields.

An alignment technique based on the combination of magnetic fields and a liquid crystal (LC) template uses the advantages of both approaches: the magnetic fields offer non-contact methods that apply to all sample sizes and shapes, whilst the LC templates offer high susceptibilities. The combination introduces a route to control the spatial organization of materials with low intrinsic susceptibilities. We demonstrate that we can unidirectionally align one such material, peptide amphiphiles in water, on a centimeter scale at a tenfold lower magnetic field by using a lyotropic chromonic liquid crystal as a template.

Directing Soft Matter in Water Using Electric Fields.

Directing the spatial organization of functional supramolecular and polymeric materials at larger length scales is essential for many biological and molecular optoelectronic applications. Although the application of electrical fields is one of the most powerful approaches to induce spatial control, it is rarely applied experimentally in aqueous solutions, since the low susceptibility of soft and biological materials requires the use of high fields, which leads to parasitic heating and electrochemical degradation. In this work, we demonstrate that we can apply electric fields when we use a mineral liquid crystal as a responsive template.

Complete chiral resolution using additive-induced crystal size bifurcation during grinding.

Grinding them down: By using a tailor-made additive, even in the absence of racemization in solution, abrasive grinding can yield an enantiopure solid state. This novel chiral resolution technique is based on an asymmetric bifurcation in the crystal size distribution as a result of stereoselective hampered crystal growth. R = o-tolyl.