Insight of the Metal–Ligand Interaction in f-Element Complexes by Paramagnetic NMR Spectroscopy

The magnetic properties of Ln^III and An^III complexes formed with dipicolinate ligands have been studied by NMR spectroscopy. To know precisely the geometries of these complexes, a crystallographic study by single-crystal X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) in solution was performed. Several methods to separate the paramagnetic shifts observed in the NMR spectra were applied to these complexes. Methods using a number of nuclei of the dipicolinate ligands revealed an abrupt change in the geometries of the complexes and a metal–ligand interaction in the middle of the lanthanide series. A study of the variation of the paramagnetic shifts with temperature demonstrated that higher-order terms of the dipolar and contact contributions are required, especially for the lightest Ln^III and almost all the studied An^III. Bleaney's parameters <S_z>_a and relating to the contact and dipolar terms, respectively, were deduced from experimental data and compared with the results of ab initio calculations. Quite a good agreement was found for the temperature dependencies of <S_z>_a and . However, the values obtained from cation magnetic anisotropy calculations showed some discrepancies with the values derived from Bleaney's equation defined for Ln^III. Other parameters, such as the crystal field parameter and the hyperfine constants F_i obtained from the experimental data of the [An(ethyl-dpa)₃]³⁻ complexes (ethyl-dpa=4-ethyl-2,6-dipicolinic acid), are at odds with the assumptions underlying Bleaney's theory.     

Simultaneous electrochemical measurement of metal and organic propellant constituents of gunshot residues

The simultaneous electrochemical measurement of heavy-metal and organic propellants relevant to gunshot residues (GSRs) is demonstrated. Cyclic voltammetry (CV) and cyclic square-wave stripping voltammetry (C-SWV) are shown to detect, in a single run, common propellants, such as nitroglycerin (NG) and dinitrotoluene (DNT), along with the heavy metal constituents of GSR, antimony (Sb), lead (Pb), zinc (Zn) and barium (Ba). The voltammetric detection of the stabilizer diphenylamine (DPA) along with inorganic constituents has also been examined. The resulting electrochemical signatures combine -in a single voltammogram- the response for the various metals and organic species, based on the reduction and oxidation peaks of the constituents. Cyclic square-wave voltammetry at the glassy carbon electrode (GCE), involving an intermittent accumulation at the reversal potentials of -0.95 V (for Sb, Pb, DNT and NG) and -1.3 V (for Sb, Pb, Zn and DPA) is particularly useful to offer distinct electrochemical signatures for these constituents of GSR mixtures, compared to analogous cyclic voltammetric measurements. Simultaneous voltammetric measurements of barium (at thin-film Hg GCE) and DNT (at bare GCE) are also demonstrated in connection to intermittent accumulation at the reversal potential of -2.4 V. Such generation of unique, single-run, information-rich inorganic/organic electrochemical fingerprints holds considerable promise for 'on-the-spot' field identification of individuals firing a weapon, as desired for diverse forensic investigations.     

A click chemistry route to 2-functionalised PEGylated and cationic β-cyclodextrins: co-formulation opportunities for siRNA delivery

A new approach to the synthesis of amphiphilic β-cyclodextrins has used 'click' chemistry to selectively modify the secondary 2-hydroxyl group. The resulting extended polar groups can be either polycationic or neutral PEGylated groups and these two amphiphile classes are compatible in dual cyclodextrin formulations for delivery of siRNA. When used alone with an siRNA, a cationic cyclodextrin was shown to have good transfection properties in cell culture. Co-formulation with a PEGylated cyclodextrin altered the physicochemical properties of nanoparticles formed with siRNA. Improved particle properties included lower surface charges and reduced tendency to aggregate. However, as expected, the transfection efficiency of the cationic vector was lowered by co-formulation with the PEGylated cyclodextrin, requiring future surface modification of particles with targeting ligands for effective siRNA delivery.     

Reorientational Dynamics of Water Confined in Zeolites

We present a detailed molecular‐dynamics study of water reorientation and hydrogen‐bond dynamics in a strong confinement situation, within the narrow pores of an all‐silica Linde type A (LTA) zeolite. Two water loadings of the zeolite are compared with the bulk case. Water dynamics are retarded in this extreme hydrophobic confinement and the slowdown is more pronounced at higher water loading. We show that water reorientation proceeds mainly by large‐amplitude angular jumps, whose mechanism is similar to that determined in the bulk. The slowdown upon hydrophobic confinement arises predominantly from an excluded‐volume effect on the large fraction of water molecules lying at the interface with the zeolite matrix, with an additional minor contribution coming from a structuring effect induced by the confinement.     

Ultrafast laser ablation of metal films on flexible substrates

For the development of organic electronics on flexible substrates, we study the potentialities of direct laser patterning of conductive films deposited on plastic foils. The materials under study are silver and platinum films (100-nm thick) deposited on Kapton^® substrates. The experiments are done using a laser source operating at 1030 nm, 500 fs, under different irradiation conditions: single and multiple pulses at various frequencies. The laser ablation thresholds are measured and the ablation morphologies are analyzed with scanning electron microscopy. The results of these investigations show that photomechanical effects lead to delamination of the film and that depending of the irradiation conditions, incubation or heat accumulation effects can occur. The experimental results are compared to simulations based on the two-temperature model. Particularly we study the heat accumulation effects that can occur in the case of multiple pulses and that are detrimental for plastic substrates.     

Electronic properties of organic monolayers and molecular devices

We review some of our recent experimental results on charge transport in organic nanostructures such as self-assembled monolayer and monolayers of organic semiconductors. We describe a molecular rectifying junction made from a sequential self-assembly on silicon. These devices exhibit a marked current-voltage rectification behavior due to resonant transport between the Si conduction band and the π molecule highest occupied molecular orbital of the π molecule. We discuss the role of metal Fermi level pinning in the current-voltage behavior of these molecular junctions. We also discuss some recent insights on the inelastic electron tunneling behavior of Si/alkyl chain/metal junctions.     

Polymer-like conformation and growth kinetics of Bi2S3 nanowires

One-dimensional inorganic crystals (i.e., crystalline nanowires) are one of the most intensely investigated classes of materials of the past two decades. Despite this intense effort, an important question has yet to be answered: do nanowires display some of the unique characteristics of polymers as their diameter is progressively decreased? This work addresses this question with three remarkable findings on the growth and form of ultrathin Bi(2)S(3) nanowires. (i) Their crystallization in solution is quantitatively describable as a form of living step-growth polymerization: an apparently exclusive combination of addition of "monomer" to the ends of the nanowires and coupling of fully formed nanowires "end-to-end", with negligible termination and initiation. (ii) The rate constants of these two main processes are comparable to those of analogous processes found in polymerization. (iii) The conformation of these nanowires is quantitatively described as a worm-like conformation analytically analogous to that of semiflexible polymers and characterized by a persistence length of 17.5 nm (shorter than that of double-stranded DNA) and contour lengths of hundreds of micrometers (longer than those of most synthetic polymers). These findings do not prove a chemical analogy between crystals and polymers (it is unclear if the monomer is a molecular entity tout court) but demonstrate a physical analogy between crystallization and polymerization. Specifically, they (i) show that the crystallization of ensembles of nanoscale inorganic crystals can be conceptually analogous to polymerization and can be described quantitatively with the same experimental and mathematical tools, (ii) demonstrate that one-dimensional nanocrystals can display topological characteristics of polymers (e.g., worm-like conformation in solution), (iii) establish a unique experimental model system for the investigation of polymer-like topological properties in inorganic crystals, and (iv) provide new heuristic guidelines for the synthesis of polymer-like nanowires.     

The diels-alder reaction of α-ethenylidene cyclanones: a stereoselective approach to spirocyclic compounds.

The BF₃:Et₂O catalysed Diele-Alder reaction of α-ethenylidene cyclanones constitutes a highly stereoselective route to spirocyclic dienones.     

A combinatorial approach to the study of particle size effects on supported electrocatalysts: oxygen reduction on gold

A novel high-throughput technique has been developed for the investigation of the influence of supported metal particle size and the support on electrocatalytic activity. Arrays with a gradation of catalyst particle sizes are fabricated in a physical vapor deposition system that also allows selection of the support material. Simultaneous electrochemical measurements at all electrodes in the array, together with determination of the actual particle size distribution on each of the electrodes by transmission electron microscopy (TEM), then allows rapid determination of the activity as a function of catalyst center size. The procedure is illustrated using data for the reduction of oxygen on gold nanoparticles supported on both substoichiometric titanium dioxide (TiO(x)()) and carbon and the conclusions are verified using voltammetry at rotating disk electrodes. Gold centers with diameters in the range 1.4-6.3 nm were investigated and it is demonstrated that, with both supports, the catalytic activity for oxygen reduction decays rapidly for particle sizes below 3.0 nm. This may be observed as a decrease in current at constant potential or an increase in the overpotential for oxygen reduction.