Stepwise fusion of porphyrin β,β'-pyrrolic positions to imidazole rings

A strategy for the stepwise annulation of pyrrolic rings of a porphyrin to imidazole rings is presented. Mono(imidazole), Janus and corner bis(imidazole), T-shaped tris(imidazole), and tetrakis(imidazole) porphyrins have been synthesized and characterized.     

Use of multiple reaction monitoring for multiplex analysis of colorectal cancer-associated proteins in human feces

Colorectal cancer (CRC) is the second most common cause of cancer-related deaths worldwide with an annual incidence of almost a million cases and an annual mortality around 500,000. The fecal occult blood test is currently the first line method for CRC screening, but has unacceptably low sensitivity and specificity. Improved screening tests are therefore urgently required for early-stage CRC screening when therapy is most likely to be effective. We describe a discovery-based proteomics hypothesis using orthogonal multi-dimensional fractionation (1-D SDS-PAGE, RP-HPLC, size exclusion chromatography) to mine deep into the fecal proteome for the initial discovery process, which generated a library containing 108 human fecal proteins with the associated peptide and MS/MS data. These data were then used to develop and optimize a multiplex multiple reaction monitoring assay for 40 non-redundant human proteins present in the feces. To show proof of principal for clinical analysis, multiplex screening of these 40 proteins was carried out on fecal samples from eight CRC patient and seven normal volunteers. We identified 24 proteins consistently found in all samples and nine proteins found only in the CRC patients, showing the potential of this approach for the analysis of potential CRC biomarkers. Absolute quantitation using C-terminal isotopically labeled synthetic peptides corresponding to hemoglobin and carcinoembryonic antigen 5 was also performed.     

Development of fast,simultaneous and multi‐technique scanning hard X‐ray microscopy at Synchrotron Soleil

A distributed fast‐acquisition system for synchronized multi‐technique experiments is presented, in which the collection of metadata and the asynchronous merging of large data volumes from multiple detectors are managed as part of the data collection process. This fast continuous scanning scheme, named FLYSCAN, enables measurement of microscopy data on a timescale of milliseconds per pixel. Proof‐of‐principle multi‐technique experiments, namely scanning X‐ray fluorescence spectrometry combined with absorption, differential phase contrast and dark‐field imaging, have been performed on biological and geological samples.     

Towards Reversible High-Voltage Multi-Electron Reactions in Alkali-Ion Batteries Using Vanadium Phosphate Positive Electrode Materials

Vanadium phosphate positive electrode materials attract great interest in the field of Alkali-ion (Li, Na and K-ion) batteries due to their ability to store several electrons per transition metal. These multi-electron reactions (from V²⁺ to V⁵⁺) combined with the high voltage of corresponding redox couples (e.g., 4.0 V vs. for V³⁺/V⁴⁺ in Na₃V₂(PO₄)₂F₃) could allow the achievement the 1 kWh/kg milestone at the positive electrode level in Alkali-ion batteries. However, a massive divergence in the voltage reported for the V³⁺/V⁴⁺ and V⁴⁺/V⁵⁺ redox couples as a function of crystal structure is noticed. Moreover, vanadium phosphates that operate at high V³⁺/V⁴⁺ voltages are usually unable to reversibly exchange several electrons in a narrow enough voltage range. Here, through the review of redox mechanisms and structural evolutions upon electrochemical operation of selected widely studied materials, we identify the crystallographic origin of this trend: the distribution of PO₄ groups around vanadium octahedra, that allows or prevents the formation of the vanadyl distortion (O^…V⁴⁺=O or O^…V⁵⁺=O). While the vanadyl entity massively lowers the voltage of the V³⁺/V⁴⁺ and V⁴⁺/V⁵⁺ couples, it considerably improves the reversibility of these redox reactions. Therefore, anionic substitutions, mainly O²⁻ by F⁻, have been identified as a strategy allowing for combining the beneficial effect of the vanadyl distortion on the reversibility with the high voltage of vanadium redox couples in fluorine rich environments.     

High‐temperature kinetics of the reaction between CN and hydrocarbons using a novel high‐enthalpy flow tube

More than 70 molecules of varied nature have been identified in the envelopes of carbon‐rich stars through their spectral fingerprints in the microwave or far infrared regions. Many of them are carbon chain molecules and radicals, and a significant number are unique to the circumstellar medium. The determination of relevant laboratory kinetics data is critical to keep up with the development of the high spectral and spatial resolution observations and of the refinement of chemical models. Neutral–neutral reactions of the CN radical with unsaturated hydrocarbons could be a dominant route in the formation of cyanopolyynes, even at low temperatures and deserve a detailed laboratory investigation. The approach we have developed aims to bridge the temperature gap between resistively heated flow tubes and shock tubes. The present kinetic measurements are obtained using a new reactor combining a high‐enthalpy source with a flow tube and a pulsed laser photolysis–laser‐induced fluorescence system to probe the undergoing chemical reactions. The high‐enthalpy flow tube has been used to measure the rate constant of the reaction of the CN radical with propane (C₃H₈), propene (C₃H₆), allene (C₃H₄), 1,3‐butadiene (1,3‐C₄H₆), and 1‐butyne (C₄H₆) over a temperature range extending from 300 to 1200 K. All studied reactions of CN with unsaturated hydrocarbons are rapid, with rate coefficients greater than 10^?10 cm³ · molecule^?1 · s^?1 and exhibit slight negative temperature dependence above room temperature. © 2012 Wiley Periodicals, Inc. Int J Chem Kinet 44: 753–766, 2012     

Gaalas-based micromachined accelerometer

Abstract

GaAlAs-based microstructures have been designed and realized in order to take advantage of their favorable intrinsic properties. Piezoresistive properties were determined on macrostructures. Microfabrication process was established and first micro-accelerometers were produced.     

Curiosities and counterexamples in smooth convex optimization

Mathematical Programming - Counterexamples to some old-standing optimization problems in the smooth convex coercive setting are provided. We show that block-coordinate, steepest descent with exact...     

Identification of Local Viscoplastic Properties in P91 Welds from Full Field Measurements at Room Temperature and 625 °C

A methodology to obtain visco-plastic laws in heterogeneous materials with digital image correlation (DIC) is proposed based on tensile and tensile-relaxation tests conducted at room temperature and at 625 °C. Tested samples are manufactured from a P91 weld in which a microstructural heterogeneity translates into graded mechanical properties. To simplify the problem, a classical decomposition of the weld into five different domains is considered. Strain field in each domain is obtained by means of digital image correlation applied to high magnification pictures recorded with an optical long distance microscope. The conducted identifications exhibit key features in the behaviour of each domain in terms of yield stress, ultimate tensile stress and hardening at both room temperature and 625 °C. Experimental fields are compared to the fields provided by finite element simulations. Eventually, the benefit of accounting for transverse strains in the identification procedure is examined, and the robustness of the procedure with addition of noise (representative of experimental conditions) in the measurement is characterized.     

Ballistic imaging of liquid breakup processes in dense sprays

Ballistic imaging is the name applied to a category of optical techniques that were originally developed for medical applications. Recently, ballistic imaging was adapted to acquire instantaneous images of the liquid core inside atomizing sprays; a region that has been heretofore inaccessible to spray researchers. An important difference between spray research and the medical imaging problem is the need for high fidelity single-shot (within 10 μs) imaging in a spray whereas stationary tissue images can be averaged. Transient ballistic imaging diagnostics have been used to reveal details of the primary breakup process in a LOX injector, a turbulent water jet, a water jet in cross-flow, a transient diesel fuel spray, a rocket fuel injector, and an aerated spray. This paper briefly discusses various methods for imaging the liquid core, it introduces ballistic imaging and provides specific examples, it describes detailed studies of photon transmission through dense media, and it then discusses incorporation of those results into a model for a ballistic imaging instrument that can evaluate and optimize various concepts.     

Strong-field molecular ionization: determination of ionization probabilities calibrated with field-free alignment

We report an original optical method providing the probability of molecular ionization induced by femtosecond laser pulses. The approach consists of exploiting molecular alignment to extract reliable information about ionization. The cross defocusing technique implemented for this purpose reveals a sensitivity with respect to postpulse alignment, as well as to the free electron density induced by the ultrashort laser pulse. The analysis of the resulting signal thus gives access to absolute single-ionization probabilities calibrated through the degree of alignment, provided that free electrons are produced mainly by single ionization. The relevance of the method is assessed in N2.