Mechanism of low temperature decomposition of NiO single crystals

The decomposition of NiO single crystal was investigated under dissociative conditions in the temperature interval between 330 and 850 °C in the absence of reducing gas species. An unusually fast and constant decomposition rate was measured at the lowest temperatures, coupled with an unusual largely porous microstructure of the metallic product layer. This anomalous high reaction rate was interpreted on the basis of a decomposition mechanism implying the dissociative vaporization of the oxide followed by the condensation of the metal. The proposed mechanism is supported by the microstructure of the product and of the reacting interface. The complex dependence of reaction rate from temperature was shown to be related to a collapse of the porous product to form a compact metal layer at higher temperatures due to sintering.     

Synthesis and spectroscopic characterization of new triorganotin(IV) complexes with the bis(1‐methyl‐1H‐imidazol‐2‐ylthio)acetate ligand: effects on trout erythrocyte components

Triorganotin(IV) derivatives containing the anionic ligand bis(1‐methyl‐1H‐imidazol‐2‐ylthio)acetate [(S‐tim)₂CHCO₂]⁻ were synthesized from the reaction between R₃SnCl acceptors (R = Me and Ph) and the sodium salt of the ligand. Mono‐nuclear complexes of the type [(S‐tim)₂CHCO₂]SnR₃ were obtained, which were fully characterized by elemental analyses and FT‐IR in the solid state, and by NMR (¹H, ¹³C and ¹¹⁹Sn) spectroscopy and electrospray ionization mass in solution. The toxic effects shown by these compounds on trout erythrocyte components showed that the toxicity of the organotin(IV) complexes depends on the nature and on the lipophilicity of the substituents on the metal centre. Copyright © 2007 John Wiley & Sons, Ltd.     

On the use of spires for generating inflow conditions with energetic coherent structures in large eddy simulation

While it has long been a practice to place spires near the inlet of a wind tunnel to quickly develop a turbulent boundary layer with similarities to an atmospheric boundary layer, this has not been the case for creating turbulent boundary layer inflow in large eddy simulations (LESs) of turbulent flows. We carry out LES with the curvilinear immersed boundary method to simulate the flow in a wind tunnel with a series of spires in order to investigate the feasibility of numerically developing inflow conditions from a precursory spire LES and assessing the similarities of the turbulence statistics to those of an atmospheric boundary layer. The simulated mean velocity field demonstrates that a turbulent boundary layer with height equal to the spire height develops very quickly, within five spire heights downstream. The major attribute of using spires for precursory simulations is the spatially evolving coherent structures that form downstream of the spires offering a range of length scales at both the vertical and streamwise directions allowing multiple turbulent inflow conditions to be extracted from a single simulation. While the distribution of length scales far from the spires resembles an atmospheric boundary layer, some turbulence statistics have some significant differences.     

Exact Electronic Bands for a Periodic Pöschl-Teller Potential

We show that supersymmetry is a simple but powerful tool to exactly solve quantum mechanics problems. Here, the supersymmetric approach is used to analyse a quantum system with periodic Pöschl-Teller potential, and to find out the exact energy spectra and the corresponding band structure.     

Effectiveness of measures of performance during speculative bubbles

Statistical analysis of financial data mostly focused on testing the validity of Brownian motion (Bm). Analyses performed on several time series have shown deviation from the Bm hypothesis, that is at the base of the evaluation of many financial derivatives. We analyze the behavior of performance measures based on maximum drawdown movements (MDD(T)), testing their stability when the underlying process deviates from the Bm hypothesis. In particular we consider the fractional Brownian motion (fBm), and fluctuations estimated empirically on raw market data. The case study of the rising part of speculative bubbles is reported.     

Three-electron auger process from beam-foil excited multiply charged ions

Electron emission from collisions of C3+ ions (22.7 A MeV) with carbon foils (21, 49 and 90 microg/cm(2)) was studied by the time-of-flight method. Two prominent emission patterns can be readily identified as "binary encounter" electrons and "cusp" electrons. With the thinnest target only, a third structure is visible at slightly lower time-of-flight (thus slightly higher energy) than the cusp electrons. The energy of these electrons would correspond to 647(+116)/(-104) eV if they were emitted from the projectile frame of reference. A possible explanation is a rare three-electron-Auger K(2)L(2)L(1) process.     

Salen‐Based Amphiphiles: Directing Self‐Assembly in Water by Metal Complexation

Tuning morphologies of self‐assembled structures in water is a major challenge. Herein we present a salen‐based amphiphile which, using complexation with distinct transition metal ions, allows to control effectively the self‐assembly morphology in water, as observed by Cryo‐TEM and confirmed by DLS measurements. Applying this strategy with various metal ions gives a broad spectrum of self‐assembled structures starting from the same amphiphilic ligand (from cubic structures to vesicles and micelles). Thermogravimetric analysis and electric conductivity measurements reveal a key role for water coordination apparently being responsible for the distinct assembly behavior.     

Water and Sodium Chloride: Essential Ingredients for Robust and Fast Pd‐Catalysed Cross‐Coupling Reactions between Organolithium Reagents and (Hetero)aryl Halides

Direct palladium‐catalysed cross‐couplings between organolithium reagents and (hetero)aryl halides (Br, Cl) proceed fast, cleanly and selectively at room temperature in air, with water as the only reaction medium and in the presence of NaCl as a cheap additive. Under optimised reaction conditions, a water‐accelerated catalysis is responsible for furnishing C(sp³)–C(sp²), C(sp²)–C(sp²), and C(sp)–C(sp²) cross‐coupled products, in competition with protonolysis, within a reaction time of 20 s, in yields of up to 99 %, and in the absence of undesired dehalogenated/homocoupling side products even when challenging secondary organolithiums serve as the starting material. It is worth noting that the proposed protocol is scalable and the catalyst and water can easily and successfully be recycled up to 10 times, with an E‐factor as low as 7.35.