Synthesis of Phenanthrene/Pyrene Hybrid Microparticles: Useful Synthetic Mimics for Polycyclic Aromatic Hydrocarbon-Based Cosmic Dust.

Polycyclic aromatic hydrocarbons (PAHs) are found throughout the interstellar medium and are important markers for the evolution of galaxies and both star and planet formation. They are also widely regarded as a major source of carbon, which has implications in the search for extraterrestrial life. Herein we construct a melting point phase diagram for a series of phenanthrene/pyrene binary mixtures to identify the eutectic composition (75 mol % phenanthrene) and its melting point (83 °C). The molten oil obtained on heating this eutectic composition to 90 °C in aqueous solution is homogenized in the presence of a water-soluble polymeric emulsifier. On cooling to 20 °C, polydisperse spherical phenanthrene/pyrene hybrid microparticles are obtained. Varying the stirring rate and emulsifier type enables the mean microparticle diameter to be adjusted from 11 to 279 µm. Importantly, the phenanthrene content of individual microparticles remains constant during processing, as expected for the eutectic composition. These new hybrid microparticles form impact craters and undergo partial fragmentation when fired into a metal target at 1 km s-1 using a light gas gun. When fired into an aerogel target at the same speed, microparticles are located at the ends of characteristic "carrot tracks". Autofluorescence is observed in both types of experiments, which at first sight suggests minimal degradation. However, Raman microscopy analysis of the aerogel-captured microparticles indicates prominent pyrene signals but no trace of the more volatile phenanthrene component. Such differential ablation during aerogel capture is expected to inform the in situ analysis of PAH-rich cosmic dust in future space missions.

Synthesis of Autofluorescent Phenanthrene Microparticles via Emulsification: A Useful Synthetic Mimic for Polycyclic Aromatic Hydrocarbon-Based Cosmic Dust.

Phenanthrene is the simplest example of a polycyclic aromatic hydrocarbon (PAH). Herein, we exploit its relatively low melting point (101 °C) to prepare microparticles from molten phenanthrene droplets by conducting high-shear homogenization in a 3:1 water/ethylene glycol mixture at 105 °C using poly(N-vinylpyrrolidone) as a non-ionic polymeric emulsifier. Scanning electron microscopy studies confirm that this protocol produces polydisperse phenanthrene microparticles with a spherical morphology: laser diffraction studies indicate a volume-average diameter of 25 ± 21 µm. Such projectiles are fired into an aluminum foil target at 1.87 km s-1 using a two-stage light gas gun. Interestingly, the autofluorescence exhibited by phenanthrene aids analysis of the resulting impact craters. More specifically, it enables assessment of the spatial distribution of any surviving phenanthrene in the vicinity of each crater. Furthermore, these phenanthrene microparticles can be coated with an ultrathin overlayer of polypyrrole, which reduces their autofluorescence. In principle, such core-shell microparticles should be useful for assessing the extent of thermal ablation that is likely to occur when they are fired into aerogel targets. Accordingly, polypyrrole-coated microparticles were fired into an aerogel target at 2.07 km s-1. Intact microparticles were identified at the end of carrot tracks and their relatively weak autofluorescence suggests that thermal ablation during aerogel capture did not completely remove the polypyrrole overlayer. Thus, these new core-shell microparticles appear to be useful model projectiles for assessing the extent of thermal processing that can occur in such experiments, which have implications for the capture of intact PAH-based dust grains originating from cometary tails or from plumes emanating from icy satellites (e.g., Enceladus) in future space missions.

Next-generation protein-based materials capture and preserve projectiles from supersonic impacts.

Extreme energy-dissipating materials are essential for a range of applications. The military and police force require ballistic armour to ensure the safety of their personnel, while the aerospace industry requires materials that enable the capture, preservation and study of hypervelocity projectiles. However, current industry standards display at least one inherent limitation, such as weight, breathability, stiffness, durability and failure to preserve captured projectiles. To resolve these limitations, we have turned to nature, using proteins that have evolved over millennia to enable effective energy dissipation. Specifically, a recombinant form of the mechanosensitive protein talin was incorporated into a monomeric unit and crosslinked, resulting in a talin shock-absorbing material (TSAM). When subjected to 1.5 km s-1 supersonic shots, TSAMs were shown to absorb the impact and capture and preserve the projectile.

Ionicity-dependent proton-coupled electron transfer of supramolecular self-assembled electroactive heterocycles.

Herein, we investigate the electrochemical properties of a class of Supramolecular Self-associated Amphiphilic salts (SSAs). We show that varying ionic strength of an SSA solution can cause a switching of the thermodynamics and kinetics of electron transfer. The effect of self-assembly on proton-coupled electron transfer has implications for the understanding of electron transfer kinetics in aqueous organic redox flow batteries, especially at high concentration where organic-organic intermolecular interactions become dominant even for highly soluble organic species.

Controllable hydrogen bonded self-association for the formation of multifunctional antimicrobial materials.

SSAs are a class of supramolecular self-associating amphiphilic salt, the anionic component of which contains a covalently bound hydrogen bond donor-acceptor motif. This results in a monomeric unit which can adopt multiple hydrogen bonding modes simultaneously. Previous investigations have shown examples of SSAs to act as antimicrobial agents against clinically relevant methicillin-resistant Staphylococcus aureus (MRSA). Herein, we report an intrinsically fluorescent SSA which can self-associate producing dimers, spherical aggregates and hydrogels dependent on solvent environment, while retaining antimicrobial activity against both model Gram-positive (MRSA) and Gram-negative (Escherichia coli) bacteria. Finally, we demonstrate the SSA supramolecular hydrogel to tolerate the inclusion of the antibiotic ampicillin, leading to the enhanced inhibition of growth with both model bacteria, and derive initial molecular structure-physicochemical property-antimicrobial activity relationships.