Caught in Action: Visualizing Dynamic Nanostructures Within Supramolecular Systems Chemistry.

Supramolecular systems chemistry has been an area of active research to develop nanomaterials with life-like functions. Progress in systems chemistry relies on our ability to probe the nanostructure formation in solution. Often visualizing the dynamics of nanostructures which transform over time is a formidable challenge. This necessitates a paradigm shift from dry sample imaging towards solution-based techniques. We review the application of state-of-the-art techniques for real-time, in situ visualization of dynamic self-assembly processes. We present how solution-based techniques namely optical super-resolution microscopy, solution-state atomic force microscopy, liquid-phase transmission electron microscopy, molecular dynamics simulations and other emerging techniques are revolutionizing our understanding of active and adaptive nanomaterials with life-like functions. This Review provides the visualization toolbox and futuristic vision to tap the potential of dynamic nanomaterials.

Rubicene, an Unusual Contorted Core for Discotic Liquid Crystals.

Rubicene, an unusual contorted polycyclic aromatic hydrocarbon, was realized to function as a novel core fragment for discotic liquid crystals. The central π-conjugated motif was prepared from dialkoxyiodobenzene via Sonagashira coupling followed by pentannulation and Scholl cyclodehydrogenation. The synthesized rubicene derivatives were found to be thermally stable and exhibit enantiotropic columnar mesophases. The columnar arrangement of these derivatives has been validated using polarising optical microscopy, differential scanning calorimetry & small-angle X-ray scattering.

Salt-induced swelling transitions of a lamellar amphiphile-Polyelectrolyte complex.

We report salt-induced swelling transitions of a lamellar complex of the anionic polyelectrolyte, poly(acrylic acid sodium salt) (PAANa), and the cationic amphiphile, didodecyldimethylammonium chloride (DDAC). Increasing the concentration of NaCl in the solution is found to lead to a collapsed → swollen → collapsed transition of the complex. The swelling transition is driven by an abrupt increase in PAANa adsorption on DDAC bilayers above a threshold salt concentration. The lamellar periodicity of the swollen phase is not determined by the thickness of the adsorption layer, and additional mechanisms have to be invoked to understand the extent of its swelling. The swelling transition is not observed for the highest molecular weight of PAANa used, but a gradual transformation between the two collapsed structures is seen on increasing the salt concentration. The polyelectrolyte chains desorb from the bilayers at a very high salt concentration, in a process similar to the well-known destabilization of complexes of oppositely charged polyelectrolytes. However, unlike the PAANa chains, the polymer-free bilayers do not disperse uniformly in the solution. Instead, they form a collapsed lamellar stack containing very little water due to the van der Waals attraction between them. The occurrence of an abrupt swelling transition at intermediate salt concentrations in this system contrasts sharply with the gradual swelling reported in other complexes with increasing salt concentration. Furthermore, this behavior does not seem to have been anticipated by theories of complexation of oppositely charged macroions. More experiments are required for a clear understanding of the interactions stabilizing the different phases observed in this system.