A low molecular weight hydrogel with unusual gel aging

We describe a dipeptide hydrogel with unusual aging characteristics. Over time, a transformation from a turbid gel to a transparent gel occurs which is initiated from the air–water interface. Here, we investigate this transition and discuss the implications of this aging on the bulk properties of the gel

Photoresponsive gelators

Low molecular weight gels can be responsive to a range of external stimuli. The use of light as an external stimulus to modify gels is of particular interest for a number of reasons. Light is a non-invasive trigger. For example, using light it is possible to spatially target a specific area of the gel leading to patterned gel surfaces. Here, we review the different approaches that have been used to form low molecular weight gels that respond to ligh

Controlling the assembly and properties of low-molecular-weight hydrogelators

Low-molecular-weight gels are formed by the self-assembly of small molecules into fibrous networks that can immobilize a significant amount of solvent. Here, we focus on our work with a specific class of gelator, the functionalized dipeptide. We discuss the current state of the art in the area, focusing on how these materials can be controlled. We also highlight interesting and unusual observations and unanswered questions in the field

Using sugar-based additives to prolong the lifetime of air-stable radicals in self-assembled perylene bisimides

Sugar‐based additives were introduced into self‐assembled worm‐like micelles of amino acid functionalized perylene bisimides. The solutions are then dried to form thin films and used as photoresponsive materials. The effects of the addition of dextran and sucrose on the properties of the perylene bisimide thin film are investigated using cross‐polarized light optical microscopy, electron paramagnetic resonance (EPR) spectroscopy, rheology, UV‐vis absorption spectroscopy and electrochemistry. The radical anion is stabilized by the presence of the additives in solution and in the thin films, resulting in a significantly increased lifetimes and persistent conductivity

Mechanoresponsive self‐assembled perylene bisimide films

In this work, self-assembled amino-acid appended perylene bisimides (PBIs) have been studied that when processed into thin films change their resistivity in response to being bent. The PBIs assemble into structures in water and form thin films upon drying. These normally delicate thin films can be tolerant to bending, depending on the aggregates they form. Furthermore, the films then reversibly change their resistivity in response to this mechanical stimulus. This change is proportional to the degree of bending of the film giving them the potential to be used quantitatively to measure mechanical movement, such as in wearable devices

Aligning self-assembled perylene bisimides in a magnetic field

Photoconductive self-assembled 1D structures can be formed by perylene bisimides. These structures are generally randomly orientated, limiting their applications as conductive wires. Here, we show that magnetic fields can be used to create highly aligned, directionally-dependent thin films. This approach leads to well-aligned structures over large areas

Creating transient gradients in supramolecular hydrogels

The self‐assembly of low molecular weight gelators in water usually produces homogeneous hydrogels. However, homogeneous gels are not always desired. Using a photoacid generator, it is shown how to form gels with a transient gradient in stiffness, proved using cavitation and bulk rheology. Small‐angle neutron scattering is used to show that the gels formed by photoacid are the result of the same structures as when using a conventional pH trigger. Patterned gels can also be formed, again with transient differences in stiffness

Reversible Photoreduction as a Trigger for Photoresponsive Gels

We present here a new type of photoresponsive, reversible low molecular weight gel. All previous examples rely on a photoisomerisation, ring-closing or dimerization. We show that photoreduction of a perylene bisimide gelator results in the formation of a stable radical anion. The formation of the radical anion results in a change in the packing of the perylene bisimides in the self-assembled aggregates, leading to a change in fibrous network and an increase in the rheological properties of the gels. An increase in the rheological properties is extremely rare for a photoresponsive gel; normally, irradiation results in a gel-to-sol transition, and the gel falling apart. As the radical anion decays, which takes several hours in air, the original gel properties are restored. This photoreduction can be cycled many times. Finally, we show that the mechanical properties are different between irradiated and nonirradiated sections in a patterned gel

Water soluble organic electrochromic materials

Organic materials in electrochromic device applications possess a number of advantages over transition metal oxides like WO3 such as ease of synthesis and tunability, flexibility, and derivability from renewable feedstocks. However, these advantages are offset by the need to use organic solvents in their processing which are often flammable and/or toxic. Therefore, it is of paramount importance to the longterm economic and environmental sustainability of organic electronics research to develop water soluble organic materials. Herein, we describe the advances made in developing water soluble organic electronic materials for electrochromic applications. We here classify electrochromic materials into two broad categories: those that transition between colourless and coloured states (Type I) and those that transition between differently coloured states (Type II). The methods by which organic electrochromes are made water soluble are described in detail along with their potential applications in order to promote research in water soluble organic electronic materials in general