Management of thermal effects in high-repetition-rate pulsed optical parametric oscillators

We report on the investigation of thermal effects in high-repetition-rate pulsed optical parametric oscillators emitting in the mid-IR. We find that the thermal load induced by the nonresonant idler absorption plays a critical role in the emergence of thermally induced bistability. We then demonstrate a significant improvement of the conversion efficiency (more than 30%) when a proper axial temperature gradient is applied to the nonlinear crystal by use of a two-zone temperature-controlled oven.     

A novel and simplified procedure for patterning hydrophobic and hydrophilic SAMs for microfluidic devices by using UV photolithography

This work describes how selective patterning of hydrophobic and hydrophilic areas inside microchannels of microfluidic devices can be achieved by combining well-known chemical protocols and standard photolithography equipment (365 nm). Two techniques have been performed and compared. The first technique is based on the preparation of self-assembled monolayers of photocleavable organosilane and the second one on photoassisted grafting (365 nm) of self-assembled monolayers (SAMs) on a silicon or glass substrate. In the first case, we begin with monolayers carrying an o-nitrobenzyl function (hydrophobic area) that is photochemically cleaved, revealing a carboxylic acid group (hydrophilic area). The problem is that the energy necessary to cleave this monolayer is too high and the reaction time is more than 1 h with 50 mW/cm(2) irradiation flux. To overcome this practical disadvantage, we propose another approach that is based on the thiol-ene reaction with benzophenone as photoinitiator. In this approach, a monolayer of mercaptopropyltrimethoxysilane (MPTS) is prepared first. Subsequently, a hydrocarbon chain is photografted locally onto the thiol layer, forming a hydrophobic surface while the reminding unmodified thiol surface is oxidized into sulfonic acid (hydrophilic area). We demonstrated the feasibility of this approach and synthesized high-quality self-assembled monolayers by UV grafting with an irradiation time of 30 s at 365 nm (50 mW/cm(2)). The modified surfaces have been characterized by contact angle measurements, X-ray photoelectron spectroscopy (XPS), AFM, and multiple internal reflection infrared spectroscopy (MIR-FTIR). The difference in the contact angles on the hydrophilic and hydrophobic surfaces reached a remarkable 77 degrees. We have also demonstrated that this method is compatible with selective surface grafting inside microfluidic channels.     

Rapid analysis of organic acids in plant extracts by capillary electrophoresis with indirect UV detection: directed metabolic analyses during metal stress

A fast, reliable capillary zone electrophoresis (CZE) method with indirect UV detection was optimized and validated to determine the main organic acids contained in plants. Citric, malic, succinic, oxalic, formic, fumaric, acetic acids, and phosphate were quantified. A rapid separation while keeping a good resolution was obtained by optimizing capillary length, separation voltage, electrolyte composition, and pH. Analyses were performed in a 30 cm uncoated fused-silica capillary (length to the detector window) in the co-electroosmotic mode with reversed electroosmotic flow and anodic detection using a -30 kV separation voltage. The pH 9.0 electrolyte contained 3 x 10(-4)mol/L tetradecyltrimethylammonium and 10(-2)mol/L trimellitate. Separation with baseline return was achieved in 100 s. Linearity, detection limits, repeatability, reproducibility, and recoveries were evaluated. Mean precision values of 0.2 and 3.4% for migration times and time-corrected peak areas, respectively, enabled accurate identification and quantification whether in standard solutions or in samples. Such performances were perfectly adapted to high-throughput routine determinations of organic acids in research or industry. Organic acids were assayed in different plant tissues and cells, including sycamore, arabidopsis, buttercup, and pea. Citrate and malate were the most abundant in all plants tested with concentrations reaching 18.9 and 22.3 micromol/g fresh matter, respectively. Cadmium effect on pea leaves metabolism was also assessed.     

First approach to the use of liquid crystal elastomers for chemical sensors

Liquid crystalline thin films elastomers that are able to bind pesticides have been developed. The synthesis involves grafting mesogen and crosslinkable groups on a polysiloxane chain in the presence of a template molecule. The molecular imprinted material is obtained after thin film deposition, UV crosslinking and washing. Experiments of readsorption of pesticide are presented. Development of a multisensor platform based on thermal and capacitive sensors is described and tests of deposition of the polymer film are presented.     

Representation, searching and discovery of patterns of bases in complex RNA structures

We describe a graph theoretic method designed to perform efficient searches for substructural patterns in nucleic acid structural coordinate databases using a simplified vectorial representation. Two vectors represent each nucleic acid base and the relative positions of bases with respect to one another are described in terms of distances between the defined start and end points of the vectors on each base. These points comprise the nodes and the distances the edges of a graph, and a pattern search can then be performed using a subgraph isomorphism algorithm. The minimal representation was designed to facilitate searches for complex patterns but was first tested on simple, well-characterised arrangements of bases such as base pairs and GNRA-tetraloop receptor interactions. The method performed very well for these interaction types. A survey of side-by-side base interactions, of which the adenosine platform is the best known example, also locates examples of similar base rearrangements that we consider to be important in structural regulation. A number of examples were found, with GU platforms being particularly prevalent. A GC platform in the RNA of the Thermus thermophilus small ribosomal subunit is in an analogous position to an adenosine platform in other species. An unusual GG platform is also observed close to one of the substrate binding sites in Haloarcula marismortui large ribosomal subunit RNA.     

Surjectivité de l'application restriction à un compact dans des classes de fonctions ultradifférentiables

Résumé Etant donnée {M _p } _p0 une suite de réels strictement positifs, on considère la classe de CarlemanC{p!M _p } (resp. BeurlingB{p!M _p }) des fonctionsf indéfiniment dérivables sur ⁿ . SoitE un sous ensemble compact de ⁿ ; on peut associer à la classeC{p!M _p } (resp.B{p!M _p }) la classe des jets de Whitney surE,C _E {p!M _p }, (resp.B _E {p!M _p }) et on a une application de restriction naturelle deC{p!M _p } dansC _E {p!M _p } (resp.B{p!M _p } dansB _E {p!M _p }).Dans ce travail, on donne des conditions sur deux suites {M _p } _p0 et {M _p } _p0 pour que l'on ait les inclusions suivantes ou Ceci est, en quelque sorte, une généralisation du problème de prolongement de Whitney.

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1-AZA-1,3-dienes. Diels-alder reactions with α, β-unsaturated hydrazones.

The α,β unsaturated hydrazone $\text{3}$ reacts regioselectivity with a wide range of dienophiles to give the corresponding [4+2] adducts. Reductive cleavage of the NN bond in the adducts gives tetrahydropyridines.     

Synthesis of hybrid dendrimer-star polymers by the RAFT process

A first generation phosphorus-containing dendrimer with twelve terminal benzyl dithiobenzoate functions was designed and subsequently used as a multifunctional agent to derive hybrid star copolymers consisting of a dendritic core surrounded by twelve polystyrene branches by reversible addition-fragmentation chain transfer (RAFT).     

Pedicelloside,nouveau phtalide isole de gentiana pedicellata wall.

The title compound, isolated from $\text{Gentiana pedicellata}$ leaves, is a new alkyl-3-phthalide characterized by an acylated side chain. It has been identified by spectral analysis as [3-(1-β-D-glucosyloxy)-2-hydroxy]benzoyl 3-(3-phthalidyl)-propyl ester.