On the structure of weight modules

Given any simple Lie superalgebra , we investigate the structure of an arbitrary simple weight -module. We introduce two invariants of simple weight modules: the shadow and the small Weyl group. Generalizing results of Fernando and Futorny we show that any simple module is obtained by parabolic induction from a cuspidal module of a Levi subsuperalgebra. Then we classify the cuspidal Levi subsuperalgebras of all simple classical Lie superalgebras and of the Lie superalgebra W. Most of them are simply Levi subalgebras of , in which case the classification of all finite cuspidal representations has recently been carried out by one of us (Mathieu). Our results reduce the classification of the finite simple weight modules over all classical simple Lie superalgebras to classifying the finite cuspidal modules over certain Lie superalgebras which we list explicitly.

     

Investigation of N‐carbamoylamino acid nitrosation by {NO + O2} in the solid‐gas phase. Effects of NOx speciation and kinetic evidence for a multiple‐stage process

Nitrosation of N‐carbamoylamino acids (CAA) by gaseous NO + O₂, an interesting synthetic pathway to amino acid N‐carboxyanhydrides (NCA), alternative to the phosgene route, was investigated on N‐carbamoyl‐valine either in acetonitrile suspension or solventless conditions, and compared to the classical nitrosating system NaNO₂ + CF₃COOH (TFA), the latter being quite less efficient in terms of either rate, stoichiometric demand, or further tractability of the product. The rate and efficiency of the NO + O₂ reaction mainly depends on the O₂/NO ratio. Evaluation of the contribution of various nitrosating species (N₂O₃, N₂O₄, HNO₂) through stoichiometric balance showed the reaction to be effected mostly by N₂O₃ for O₂/NO ratios below 0.3, and by N₂O₄ for O₂/NO ratios above 0.4. The relative contribution of (subsequently formed) HNO₂ always remains minor. Differential scanning calorimetry (DSC) monitoring of the reaction in the solid phase by either HNO₂ (from NaNO₂ + TFA), gaseous N₂O₄ or gaseous N₂O₃, provides the associated rate constants (ca. 0.1, 2 and 10⁸ s^?1 at 25°C, respectively), showing that N₂O₃ is by far the most reactive of these nitrosating species. From the DSC measurement, the latent heat of fusion of N₂O_3, 2.74 kJ · mol^?1 at ?105 °C is also obtained for the first time. The kinetics was investigated under solventless conditions at 0°C, by either quenching experiments or less tedious, rough calorimetric techniques. Auto‐accelerated, parabolic‐shaped kinetics was observed in the first half of the reaction course, together with substantial heat release (temperature increase of ca. 20°C within 1–2 min in a 20‐mg sample), followed by pseudo‐zero‐order kinetics after a sudden, important decrease in apparent rate. This kinetic break is possibly due to the transition between the initial solid‐gas system and a solid‐liquid‐gas system resulting from water formation. Overall rate constants increased with parameters such as the specific surface of the solid, the O₂/NO ratio, or the presence of moisture (or equivalently the hydrophilicity of the involved CAA), however without precise relationship, while the last two parameters may directly correlate to the increasing acidity of the medium. Copyright © 2007 John Wiley & Sons, Ltd.     

An evaluation of the growth of nitrides on semipolar substrates using two indicators

We evaluate the properties of nitride heterostructures on semipolar substrates using two indicators: the cancellation of the Quantum Confined Stark Effect and the volume density of elastic energy stored in the strained layers of GaN–GaInN heterostructures lattice‐matched to (hkl)‐oriented GaN semipolar substrates. These two parameters indicate that the growth on specific orientations is a plus when compared to growth on (0001) polar substrates. We will show that, unfortunately, one cannot simultaneously minimize the stored elastic energy and cancel the Quantum Confined Stark Effect, but it is possible to significantly reduce both of them. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Organocatalytic depolymerization of poly(ethylene terephthalate)

We describe the organocatalytic depolymerization of poly(ethylene terephthalate) (PET), using a commercially available guanidine catalyst, 1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene (TBD). Postconsumer PET beverage bottles were used and processed with 1.0 mol % (0.7 wt %) of TBD and excess amount of ethylene glycol (EG) at 190 °C for 3.5 hours under atmospheric pressure to give bis(2‐hydroxyethyl) terephthalate (BHET) in 78% isolated yield. The catalyst efficiency was comparable to other metal acetate/alkoxide catalysts that are commonly used for depolymerization of PET. The BHET content in the glycolysis product was subject to the reagent loading. This catalyst influenced the rate of the depolymerization as well as the effective process temperature. We also demonstrated the recycling of the catalyst and the excess EG for more than 5 cycles. Computational and experimental studies showed that both TBD and EG activate PET through hydrogen bond formation/activation to facilitate this reaction. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Electrochemical genosensor based on three-dimensional DNA polymer brushes monolayers

A new approach to the three dimensional integration of short DNA strands at gold electrode surfaces via the in situ formation of DNA-acrylamide conjugates is presented. Surface initiated atom transfer radical polymerisation was employed to grow acrylamide brushes co-polymerised in the presence of acrylamide modified DNA probes. This strategy was demonstrated for the realisation of biofunctionalised thin polymer films capable of binding its complementary 105-base DNA amplicon. The synthesised brushes were characterised using atomic force microscopy, attenuated total reflectance spectroscopy and electrochemical impedance spectroscopy. Once characterised, the polymer brushes were applied to the quantitative detection of target DNA using an enzyme labelled reporter DNA probe in a sandwich-type format.     

Thermo-oxidation behaviour of composite materials at high temperatures: A review of research activities carried out within the COMEDI program

The present paper presents a review of the main activities carried out within the context of the COMEDI research program, a joint collaboration involving three research teams focusing on the thermo-oxidation behaviour of composite materials at high temperatures.The scientific aim of the COMEDI research program was to better identify the link between the physical mechanisms involved in thermo-oxidation phenomena: oxygen reaction-diffusion, chemical shrinkage strain/stress, degradation at different scales and to provide tools for predicting the thermo-oxidation behaviour of composite materials under thermo-oxidative environments including damage onset.This aim was accomplished by investigating experimentally the thermo-oxidation behaviour of pure resin samples - both industrial and “model” materials - and by interpreting the results by a coupled reaction-diffusion-mechanics multiphysics model.A dedicated numerical model tool has been developed and implemented into the ABAQUS^® finite element commercial software. This tool was employed to simulate the thermo-oxidative behaviour of a fibre-matrix microscopic representative composite cell.Finally, the model predictions for the composite have been validated by comparing the experimental and the simulated local matrix shrinkage displacements and the mass loss of composite specimens.     

Measurement of Total and Unbound Mycophenolic Acid and Its Glucuronide by LC Coupled with MS. Application to a Pharmacokinetic Study of Mycophenolate Mofetil in Patients with Autoimmune Diseases

Liquid chromatography coupled with mass spectrometry for the determination of total and unbound mycophenolic acid and its major metabolite in human plasma has been developed. Sample preparations were based on a fully automated solid-phase extraction process and ultrafiltration. Mass spectrometric data were acquired in a single-ion monitoring method. The analytes and nevirapine (internal standard) were well separated in an isocratic mode over 8 min. Validation study exhibited excellent linearity, with intra- and inter-day precision and accuracy of less than 12%. The assay was successfully applied to the pharmacokinetic study of mycophenolic acid in patients with autoimmune diseases.     

Synthetic studies towards diazepanone scaffolds

The synthesis of new enantiopure polyfunctionalised diazepanone scaffolds is described. The key steps involve the opening of an azido-epoxide C4 building block derived from l-ascorbic or d-isoascorbic acid by a l-serine derivative followed by a lactonisation–lactamisation two-step sequence.