Tuning the polarization along linear polyaromatic strands for rationally inducing mesomorphism in lanthanide nitrate complexes

The opposite orientation of the ester spacers in the rodlike ligands L 4C12 (benzimidazole-OOC-phenyl) and L 5C12 (benzimidazole-COO-phenyl) drastically changes the electronic structure of the aromatic systems, without affecting their meridional tricoordination to trivalent lanthanides, Ln(III), and their thermotropic liquid crystalline (i.e., mesomorphic) behaviors. However, the rich mesomorphism exhibited by the complexes [Ln(L 4C12)(NO3)3] (Ln=La-Lu) vanishes in [Ln(L 5C12)(NO3)3], despite superimposable molecular structures and comparable photophysical properties. Density functional theory (DFT) and time-dependant DFT calculations performed in the gas phase show that the inversion of the ester spacers has considerable effects on the electronic structure and polarization of the aromatic groups along the strands, which control residual intermolecular interactions responsible for the formation of thermotropic liquid-crystalline phases. As a rule of thumb, an alternation of electron-poor and electron-rich aromatic rings favors intermolecular interactions between the rigid cores and consequently mesomorphism, a situation encountered for L 4C12, L 5C12, [Ln(L 4C12)(NO3)3], but not for [Ln(L 5C12)(NO3)3]. The intercalation of an additional electron-rich diphenol ring on going from [Ln(L 5C12)(NO3)3] to [Ln(L 6C12)(NO3)3] restores mesomorphism despite an unfavorable orientation of the ester spacers, in agreement with our simple predictive model.     

Theoretical investigation of the adsorption of methanol on the (110) surface of γ-alumina

The adsorption of methanol on the (110) surface of γ-alumina was investigated using both ab initio and density functional theory quantum chemical methods. A [Al₃O₉H₁₀]⁺ cluster model comprising one tetrahedral and two octahedral aluminum cations were used to describe the surface and the mechanism of adsorption of methanol. This has allowed us to rationalize the stable structures of adsorbate and the mode of bonding. The IR frequency shifts between the gas phase and the adsorbed species were also calculated and they exhibit good agreement with experiment.     

Synthesis of novel graft polyhydroxyalkanoates

Graft copolymers were synthesized by direct condensation of methoxy-poly(ethylene glycol) (MePEG) or methoxy-poly(lactic acid) (MePLA) onto a reactive polyhydroxyalkanoate (PHA) backbone in organic solvent. Side carboxylic groups of the PHA were coupled with end hydroxyl groups of MePEG or MePLA in the presence of N,N′-dicylohexylcarbodiimide (DCC). Graft copolymers were characterized by ¹H NMR spectroscopy and size exclusion chromatography (SEC). NMR spectra of PHA-g-PEG and PHA-g-PLA showed the presence of significant amounts of PEG and PLA, respectively. No noticeable unreacted PEG or PLA were detected in SEC chromatograms. Grafting of hydrophilic polymers chains as PEG or biodegradable oligomers as PLA onto PHA backbone will generate polyesters with a more rapid water uptake and faster biodegradation rates. These PHA polymers conjugates could be interesting for bioactive agent delivery systems.     

A nodal discontinuous Galerkin finite element method for nonlinear elastic wave propagation

A nodal discontinuous Galerkin finite element method (DG-FEM) to solve the linear and nonlinear elastic wave equation in heterogeneous media with arbitrary high order accuracy in space on unstructured triangular or quadrilateral meshes is presented. This DG-FEM method combines the geometrical flexibility of the finite element method, and the high parallelization potentiality and strongly nonlinear wave phenomena simulation capability of the finite volume method, required for nonlinear elastodynamics simulations. In order to facilitate the implementation based on a numerical scheme developed for electromagnetic applications, the equations of nonlinear elastodynamics have been written in a conservative form. The adopted formalism allows the introduction of different kinds of elastic nonlinearities, such as the classical quadratic and cubic nonlinearities, or the quadratic hysteretic nonlinearities. Absorbing layers perfectly matched to the calculation domain of the nearly perfectly matched layers type have been introduced to simulate, when needed, semi-infinite or infinite media. The developed DG-FEM scheme has been verified by means of a comparison with analytical solutions and numerical results already published in the literature for simple geometrical configurations: Lamb's problem and plane wave nonlinear propagation.     

All-optical generation of 40 Gb/s single sideband signals using a fiber Bragg grating

In this work, we demonstrate a reliable all-optical technique for performing optical double sideband (ODSB) to single sideband (OSSB) format conversion of a 40 Gb/s non-return-to-zero signal. It is based on the optimization of a detuned optical filter, which was implemented on a fiber Bragg grating (FBG) with a complex apodization profile. An OSSB signal with negligible distortion was obtained, as the FBG presented a nearly ideal frequency response. Higher tolerance to chromatic dispersion enabled by the OSSB signal in comparison to the ODSB signal was demonstrated on both simulation and experimental results.     

New Reactions with Thioaldehydes and Thienium Cations

Abstract

i) When generated under FVT conditions α-imino-thioaldehydes undergo a cyclization to dihydro-1,3-thiazoles. ii) Thienium cations, generated during a Pummerer reaction, can be trapped with dienes.     

Thermodynamics, structure and properties of polynuclear lanthanide complexes with a tripodal ligand: insight into their self-assembly

Self-assembly processes between a tripodal ligand and Ln(III) cations have been investigated by means of supramolecular analytical methods. At an equimolar ratio of components, tetranuclear tetrahedral complexes are readily formed in acetonitrile. The structural analysis of the crystallographic data shows a helical wrapping of binding strands around metallic cations. The properties of this series of highly charged 3D compounds were examined by using NMR spectroscopy and optical methods in solution and in the solid state. In the presence of excess metal, a new trinuclear complex was identified. The X-ray crystal structure elucidated the coordination of metallic cations with two ligands of different conformations. By varying the metal/ligand ratio, a global speciation of this supramolecular system has been evidenced with different spectroscopic methods. In addition, these rather complicated equilibria were successfully characterised with the thermodynamic stability constants. A rational analysis of the self-assembly processes was attempted by using the thermodynamic free energy model and the impact of the ligand structure on the effective concentration is discussed.     

N-Fmoc-α-sulfo-β-alanine: a versatile building block for the water solubilisation of chromophores and fluorophores by solid-phase strategy

An easy and efficient solid-phase synthesis strategy to obtain rapidly water-soluble chromophores/fluorophores in highly pure form has been developed. This first successful use of N-Fmoc-α-sulfo-β-alanine as a SPPS building block opens the way to the future development of promising direct "on-resin" peptide labelling and water-solubilising methods.