Writing Reusable Digital Geometry Algorithms in a Generic Image Processing Framework

Digital Geometry software should reflect the generality of the underlying mathe- matics: mapping the latter to the former requires genericity. By designing generic solutions, one can effectively reuse digital geometry data structures and algorithms. We propose an image processing framework focused on the Generic Programming paradigm in which an algorithm on the paper can be turned into a single code, written once and usable with various input types. This approach enables users to design and implement new methods at a lower cost, try cross-domain experiments and help generalize resultsComment: Workshop on Applications of Discrete Geometry and Mathematical Morphology, Istanb : France (2010

Multiple-Bridged Bis-Tetrathiafulvalenes: New Synthetic Protocols and Spectroelectrochemical Investigations

Synthetic strategies for preparing dimeric tetrathiafulvalenes (TTFs) linked by either one, two, or four bridges have been developed. In particular, we report efficient few-step protocols for the preparation of face-to-face overlapped quadruple-bridged bis-TTFs. The ready interconversion of cis and trans TTFs in the presence of catalytic amounts of acid was implemented in one synthetic protocol as a way to control the isomeric outcome. The compounds were characterized by NMR spectroscopy, mass spectrometry, and elemental analysis. Moreover, the X-ray crystal structure of the macrocycle 4b is presented and compared to semiempirical (PM3) geometry optimizations. Cyclic voltammetry and spectroelectrochemistry were used to describe the interactions established between two TTF units upon oxidation, that is, their ability to form mixed-valence complexes and π-dimers either intra- or intermolecularly. The length, flexibility, and number of bridging units in a bis-TTF, as well as the specific TTF positions being connected, determine the extent of these interactions. Thus, rigid linkers enhance the formation of intermolecular mixed-valence complexes. For 4b, the absorption spectrum of this mixed-valence state of TTF in solution has been recorded for the first time. Finally, preliminary complexation experiments with different electron-deficient molecules are described

3,4-Vinylenedioxythiophene (VDOT): a new building block for thiophene-based π-conjugated systems

The synthesis of the title compound and its use as a building block in π-conjugated systems are presented

Effects of structural factors on the pi-dimerization and/or disproportionation of the cation radical of extended TTF containing thiophene-based pi-conjugated spacers.

The electrochemical and chemical oxidation of extended TTF 4 and 5 are analysed by cyclic voltammetry, Visible/NIR and ESR spectroscopies, and the X-ray structures of the new salts 5·BF4(CH2Cl2) and 4·ClO4(THF)1/2 are presented. The effects of structural factors on the π-dimerization or the disproportionation reaction of the cation radical are shown. The oxidation of compound 4 presents the successive formation of stable cation radical and dication species both in dichloromethane (DCM) and in a CH3CN/THF mixture. In contrast, for compound 5, the stability of the oxidation states strongly depends on the nature of the solvent. In DCM, the oxidation of 5 proceeds by two close one-electron transfers while in CH3CN/THF the dication is directly formed via a two-electron process. The X-ray structures of the two salts reveal the formation of pi-dimers of cation radical. While the dimer (5(2))2+ is due mainly to π–π interactions between the conjugating spacer, the multiplication of the sulfur atoms in compound 4 contributes to stabilize the dimer by the combined effects of S–S and π–π interactions. Visible/NIR and ESR experiments confirm the higher tendency of 4+· to dimerize with the occurrence of dimer and monomer in solution, while for 5+· only the monomer is detected in DCM. On the other hand, by dissolution of 5·BF4(CH2Cl2) in CH3CN, only the neutral and the dicationic states of compounds 5 are observed owing to the disproportionation reaction

Diagnosis and Management of Field Pollution in the Case of an Organochlorine Pesticide, the Chlordecone

International audienc

On making nD images well-composed by a self-dual local interpolation

International audienceNatural and synthetic discrete images are generally not well-composed, leading to many topological issues: connectivities in binary images are not equivalent, the Jordan Separation theorem is not true anymore, and so on. Conversely, making images well-composed solves those problems and then gives access to many powerful tools already known in mathematical morphology as the Tree of Shapes which is of our principal interest. In this paper, we present two main results: a characterization of 3D well-composed gray-valued images; and a counter-example showing that no local self-dual interpolation satisfying a classical set of properties makes well-composed images with one subdivision in 3D, as soon as we choose the mean operator to interpolate in 1D. Then, we briefly discuss various constraints that could be interesting to change to make the problem solvable in nD

A promising method for efficient analysis of secondary metabolites in plant extracts by a matrix-free Desorption/Ionization on self-Assembled Monolayer Surfaces (DIAMS) technique

Plants are one of the major sources for the biologically active organic compounds and play a key role in medicinal chemistry for the treatment of various diseases [1]. DIAMS method is able to determine the secondary metabolites of complex vegetal extracts. The high throughput analyses of vegetal extracts are relatively difficult to perform in MALDI mass spectrometry, since the preparation of the sample involves the co-crystallization of the matrix with the analyte. Moreover irradiation of the matrix ion produces many low-m/z vs high-intensity ions preventing the detection of low molecular weight molecules such as secondary metabolites. We have developed a matrix-free alternative to MALDI analyses by the means of an original desorption/ionization on self-assembled monolayers surfaces (DIAMS) technique [2]. Monolayers were formed by using novel thiophene and coumarin-triazole analogues that absorbs the laser beam at 337nm. We herein disclose our findings with respect to the DIAMS method which is well suitable for the detection and quantification of the low molecular weight compounds that are present in plant extracts. Some of the isoquinoline alkaloids from the root extracts of Thalictrum flavum have been detected by the DIAMS method. Indeed, this technique would be promising suitable for the qualitative and quantitative analysis of polar and non-polar organic components that are widely distributed in the plants, without any preliminary chromatographic resolution [3]

Controlling the Host-Guest Interaction Mode through a Redox Stimulus

A proof-of-concept related to the redox-control of the binding/releasing process in a host-guest system is achieved by designing a neutral and robust Pt-based redox-active metallacage involving two extended-tetrathiafulvalene (exTTF) ligands. When neutral, the cage is able to bind a planar polyaromatic guest (coronene). Remarkably, the chemical or electrochemical oxidation of the host-guest complex leads to the reversible expulsion of the guest outside the cavity, which is assigned to a drastic change of the host-guest interaction mode, illustrating the key role of counteranions along the exchange process. The reversible process is supported by various experimental data (1 H NMR spectroscopy, ESI-FTICR, and spectroelectrochemistry) as well as by in-depth theoretical calculations performed at the density functional theory (DFT) level

Lithium n-Doped Polyaniline as a High-Performance Electroactive Material for Rechargeable Batteries

The discovery of conducting lithium-doped polyaniline with reversible redox chemistry allows simultaneous unprecedented capacity and stability in a non-aqueous Li battery. This compound (lithium emeraldinate) was synthesized by lithium–proton exchange on the emeraldine base in an anhydrous lithium-based electrolyte. A combination of UV/Vis-NIR spectroelectrochemistry, XPS, FTIR, and EQCM characterization allowed a unified description of the chemical and electrochemical behavior, showing facile charge delocalization of the doped states and the reversibility of the redox processes in this form of polyaniline. From a practical point of view, lithium emeraldinate behaves as a high-capacity organic active material (230 mAh g−1) that enables preparation of relatively thick composite electrodes with a low amount of carbon additives and high energy density (460 Wh kg−1). Concomitantly, at 1C rate, 400 cycles were achieved without significant capacity loss, while the coulombic efficiency is greater than 99 %