Ultrasonic Studies of Solid Azobenzene-Decorated Polymer Thin Films.

This work investigates the effect of ultrasound on switching of azobenzene isomers to their trans counterparts in solid films of methyl methacrylate and methacryloyloxyazobenzene copolymers [P(MMA/MOAB)]. Ultraviolet-visible and H nuclear magnetic resonance spectroscopies demonstrate that 46% of the cis isomer converts to the trans form purely by ultrasonic agitation and 46% converts to the trans isomer by localized ultrasound-induced heating effects. Comparative studies of isomerization by ultrasound wave, heat, and visible irradiation show that ultrasound exposure requires a longer time to switch the cis-to-trans conformation.

Nonlinear ptychographic coherent diffractive imaging.

Ptychographic Coherent diffractive imaging (PCDI) is a significant advance in imaging allowing the measurement of the full electric field at a sample without use of any imaging optics. So far it has been confined solely to imaging of linear optical responses. In this paper we show that because of the coherence-preserving nature of nonlinear optical interactions, PCDI can be generalised to nonlinear optical imaging.

Metal-organic fireworks: MOFs as integrated structural scaffolds for pyrotechnic materials.

A new approach to formulating pyrotechnic materials is presented whereby constituent ingredients are bound together in a solid-state lattice. This reduces the batch inconsistencies arising from the traditional approach of combining powders by ensuring the key ingredients are 'mixed' in appropriate quantities and are in intimate contact. Further benefits of these types of material are increased safety levels as well as simpler logistics, storage and manufacture.

Mechanical properties of β-HMX.

Background: For a full understanding of the mechanical properties of a material, it is essential to understand the defect structures and associated properties and microhardness indentation is a technique that can aid this understanding.

Results: The Vickers hardness on (010), {011} and {110} faces lay in the range of 304-363 MPa. The Knoop Hardnesses on the same faces lay in the range 314-482 MPa.

Growth and dislocation studies of β-HMX.

Background: The defect structure of organic materials is important as it plays a major role in their crystal growth properties. It also can play a subcritical role in "hot-spot" detonation processes of energetics and one such energetic is cyclotetramethylene-tetranitramine, in the commonly used beta form (β-HMX).

Results: The as-grown crystals grown by evaporation from acetone show prismatic, tabular and columnar habits, all with {011}, {110}, (010) and (101) faces.

Enforcing Ostwald's rule of stages: isolation of paracetamol forms III and II.

We have been able to isolate and study the polymorphic form III of paracetamol using a specially designed methodology. Our work represents the first report of a reproducible, reliable route to form III. This has been an outstanding problem for over quarter of a century.

Nanoparticle-coated microcrystals.

Coprecipitation provides a rapid high-yield method for self-assembly of nanoparticles on the surface of flat water-soluble crystalline surfaces and a simple immobilisation technique prior to storage or thermal and chemical modification.

Cephalexin: a channel hydrate.

The antibiotic cephalexin [systematic name: D-7-(2-amino-2-phenylacetamido)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid] forms a range of isomorphic solvates, with the maximum hydration state of two water molecules formed only at high relative humidities.

Two new paracetamol/dioxane solvates--a system exhibiting a reversible solid-state phase transformation.

This work reports on the crystal structures of two dioxane solvates of paracetamol that are true polymorphs. The high temperature phase is an orthorhombic form, space group Pbca, Z = 8, a = 12.6078(3) A, b = 12.

Polymorphism in 2,4,6-trinitrotoluene crystallized from solution.

An examination has been made of the role of solvent type in the definition of the polymorphic nature of 2,4,6-trinitrotoluene precipitated from solution. A combination of calorimetric and structural techniques including in situ crystallization studies using synchrotron radiation has shown that the variations in polymorphic form following precipitation from solution do not arise specifically from any stereospecific guidance that the nature of the solvent might impose on the structural form. Rather the differences are linked to the variations in solubility and hence supersaturation which might build up prior to nucleation and growth and to the isolation of the metastable orthorhombic phase from the solvent.