Self-organized spiral columns in laterally grafted rods.

Attachment of a flexible coil on the mid-part of a rigid rod block generates T-shaped rod-coil block molecules that self-assemble into a stepped column. These layers, in turn, self-curve into a spiral column with tunable core structure in the solid state.

Chiral assembly from achiral rod-coil molecules triggered by compression at the air-water interface.

A series of achiral rod-coil molecules consisting of an oligo(p-phenylene) conjugated rod with a poly(ethylene oxide) or poly(propylene oxide) coil laterally attached through an imidazole linkage were synthesized, and their interfacial behaviors were investigated. Compounds 1a and 1b have a similar surface behavior with a shoulder indicating a transformation of rod segments from flat-on to vertical orientation. Interestingly, CD and AFM suggest chiral films are formed when the LB films were deposited after the shoulder.

Solid-state scrolls from hierarchical self-assembly of T-shaped rod-coil molecules.

On a roll: Attachment of flexible coils to the middle of a rigid rod generates T-shaped rod-coil molecules that self-assemble into layers that roll up to form filled cylindrical and hollow tubular scrolls, depending on the coil length, in the solid state (see picture); the rods are arranged parallel to the layer plane.

Stepped strips from self-organization of oligo(p-phenylene) rods with lateral dendritic chains.

We have demonstrated that the rod segments with lateral dendritic chains self-assemble into unique stepped strips in which the rods are aligned parallel to the strip long axis. This unique organization of the rod segments arises from a balance between the energetic gain of a parallel arrangement of the rods and the resulting entropic penalty associated with stretching of the lateral flexible chains.

Aqueous self-assembly of aromatic rod building blocks.

One of the most fascinating subjects in areas such as nanoscience and biomimetic chemistry is concerned with the construction of novel supramolecular nanoscopic architectures with well defined shapes and functions. Supramolecular assemblies of aromatic rod molecules provide a facile entry into this area. Aromatic rigid rod molecules consisting of hydrophilic flexible chains, in aqueous solution can self-assemble into a variety of supramolecular structures through mutual interactions between aromatic rod molecules and water, including hydrophobic and hydrophilic interactions and pi-pi interaction.

Nanofibers from self-assembly of an aromatic facial amphiphile with oligo(ethylene oxide) dendrons.

Novel block facial amphiphiles consisting of a laterally extended aromatic segment and oligo(ethylene oxide) dendrons as a flexible segment were synthesized in a stepwise fashion and their aggregation behavior was investigated in aqueous solution; self-assembly into elongated nanofibers with a uniform diameter of 7 +/- 0.5 nm and lengths up to several hundred nanometers was observed.

Controlled self-assembly of carbohydrate conjugate rod-coil amphiphiles for supramolecular multivalent ligands.

Carbohydrate conjugate rod-coil amphiphiles were synthesized and their self-assembling behavior in aqueous solution was investigated. These amphiphiles were observed to self-assemble into supramolecular structures that differ significantly depending on the molecular architecture. The rod-coil amphiphiles based on a short coil (1) self-assemble into a vesicular structure, while the amphiphiles with a long coil (2) show a spherical micellar structure.