Activation barriers in the homolytic cleavage of radicals and ion radicals

As revealed by several experimental examples, radicals and ion radicals may, in contrast with closed-shell molecules, undergo exothermic homolytic cleavages (.A..B --> A: +.B) with substantial activation barriers. A two-state semiclassical model is proposed for explaining the existence of the barrier and estimating its magnitude. It is based on the intersection of the potential energy surfaces characterizing the dissociation of a bonding state, .A..B -->.A. +.B, on one hand, and the approach to bonding distance of a repulsive state, A: +.B --> A therefore B, on the other. After inclusion of the bond cleavage and formation as Morse curves in the normal-mode analysis, a simple activation driving force relationship is obtained, the two main ingredients of the intrinsic barrier being the triplet excitation energy of the A moiety and the pi*--> sigma* excitation energy in .A-B. The model is then tested by quantum chemical calculations, first on a simplified system to evaluate the calculation techniques and then on a real system. A comparison of the model predictions with experiment is finally performed using the rate data recently gathered for the cleavage of 4-cyanophenyl alkyl ether anion radicals, which cover a respectable range of driving forces, showing satisfactory agreement between theoretical predictions and experimental data.     

The analysis of elliptic families

In this paper we specialize the results obtained in [BF1] to the case of a family of Dirac operators. We first calculate the curvature of the unitary connection on the determinant bundle which we introduced in [BF1].We also calculate the odd Chern forms of Quillen for a family of self-adjoint Dirac operators and give a simple proof of certain results of Atiyah-Patodi-Singer on êta invariants.We finally give a heat equation proof of the holonomy theorem, in the form suggested by Witten [W 1, 2].     

Novel chemico-mechanical approach towards long-term implantable glucose sensing

The proof of concept of a continuously sensing affinity device based on the glucose-dependent viscosity of a sensitive solution containing dextran and Concanavalin A has been successfully demonstrated. The biosensor incorporates a piezoelectric diaphragm and a flow-resisting microchannel for viscosity detection, and a free-standing Anodic Alumina Oxide (AAO) porous nano-membrane as glucose selective interface. Extensive in vitro glucose measurements between two physiologically relevant glucose concentrations, 2 mM and 9 mM (respectively hypo- and hyperglycemia), were successfully performed during 4 days. To the best of our knowledge, such reversibility and stability of glucose measurement over time had not been reported yet.     

The use of power transfer matrices in predicting system loss: Theory and experiment

The phase space diagram for parabolic and step index fibers leads to a graphic representation of the bound, leaky, and refracted rays of ray theory. This concept is used to predict the attenuation of typical components of local area networks. The technique uses power transfer matrices to track the evolution of power distribution in ray packets. In particular, we predict and then measure the power transfer of two ray packets for a step index fiber. The comparison is encouraging.     

Exploring catalytic solid/liquid interfaces by in situ attenuated total reflection infrared spectroscopy

In situ attenuated total reflection Fourier transform infrared (ATR-FT-IR) spectroscopy has gained considerable attention as a powerful tool for exploring processes occurring at solid/liquid and solid/liquid/gas interfaces as encountered in heterogeneous catalysis and electrochemistry. Understanding of the molecular interactions occurring at the surface of a catalyst is not only of fundamental interest but constitutes the basis for a rational design of heterogeneous catalytic systems. Infrared spectroscopy has the exceptional advantage to provide information about structure and environment of molecules. In the last decade, in situ ATR-FT-IR has been developed rapidly and successfully applied for unraveling processes occurring at solid/liquid interfaces. Additionally, the kinetics of complex reactions can be followed by quantifying the concentration of products and reactants simultaneously in a non-destructive way. In this tutorial review we discuss some key aspects which have to be taken into account for successful application of in situ ATR-FT-IR to examine solid/liquid catalytic interfaces, including different experimental aspects concerned with the internal reflection element, catalyst deposition, cell design, and advanced experimental methods and spectrum analysis. Some of these aspects are illustrated using recent examples from our research. Finally, the potential and some limitations of ATR will be elucidated.     

Self-induced "electroclick" immobilization of a copper complex onto self-assembled monolayers on a gold electrode

We report the self-induced "electroclick" immobilization of the [Cu(II)(6-ethynyl-TMPA)(H(2)O)](2+) complex, by its simple electro-reduction, onto a mixed azidoundodecane-/decane-thiol modified gold electrode. The redox response of the grafted [Cu(II/I)(TMPA)] at the modified electrode is fully reversible indicating no Cu coordination change and a fast electron transfer.     

Synthesis and characterization of high surface area TiO2/SiO2 mesostructured nanocomposite

Recently titania synthesis was reported using various structuration procedures, leading to the production of solid presenting high surface area but exhibiting moderate thermal stability. The study presents the synthesis of TiO₂/SiO₂ nanocomposites, a solid that can advantageously replace bulk titania samples as catalyst support. The silica host support used for the synthesis of the nanocomposite is a SBA-15 type silica, having a well-defined 2D hexagonal pore structure and a large pore size. The control of the impregnation media is important to obtain dispersed titania crystals into the porosity, the best results have been obtained using an impregnation in an excess of solvent. After calcination at low temperature (400 °C), nanocomposites having titania nanodomains (～2–3 nm) located inside the pores and no external aggregates visible are obtained. This nanocomposite exhibits high specific surface area (close to that of the silica host support, even with a titania loading of 55 wt.%) and a narrow pore size distribution. Surprisingly, the increase in calcination temperature up to 800 °C does not allow to detect the anatase to rutile transition. Even at 800 °C, the hexagonal mesoporous structure of the silica support is maintained, and the anatase crystal domain size is evaluated at ～10 nm, a size close to that of the silica host support porosity (8.4 nm). Comparison of their physical properties with the results presented in literature for bulk samples evidenced that these TiO₂/SiO₂ solids are promising in term of thermal stability.     

The use of Herschel–Quincke tubes to improve the efficiency of lined ducts

The scattering matrix results of Herschel–Quincke (HQ) resonators installed in combination with an acoustic liner (HQ-Liners) are presented in this paper. This approach aims at controlling both tonal and broadband noise to improve the liner efficiency. It uses circumferential arrays of Herschel–Quincke tubes on a main duct in a serial association with a locally reacting liner of known impedance. Results for the scattering matrix of this system are deduced from an analytical model and compared with experimental and numerical data showing a good agreement. Analysis of the scattering matrix coefficients points out the modal conversion properties that depend on the number of HQ tubes along the circumference. Results of the transmission loss show that the choice of an optimal HQ configuration with respect to the liner properties can substantially improve the liner efficiency.