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61.
Philippe Bertani Jsus Raya Pierre Reinheimer Rgis Gougeon Luc Delmotte Jrme Hirschinger 《Solid state nuclear magnetic resonance》1999,13(4):255-229
19F/29Si Hartmann–Hahn continuous wave cross-polarization (CP) has been applied under fast magic-angle spinning (MAS) to a powder sample of octadecasil. Strong oscillations occur during CP on a sideband matching condition between the isolated 29Si–19F spin pairs formed by the silicons in the D4R units and the fluoride anions. The magnitude of the dipolar coupling constant was deduced directly from the line-splitting between the intense singularities of the Pake-like patterns obtained by Fourier transformation of the oscillatory polarization transfer. The corresponding Si–F internuclear distance, r=2.62±0.05 Å, is found to be in very good agreement with the X-ray crystal structure and the value of 2.69±0.04 Å recently reported from rotational echo double resonance (REDOR) and transferred echo double resonance (TEDOR) nuclear magnetic resonance (NMR) experiments. Furthermore, the CP technique is still reliable under fast MAS where both REDOR and TEDOR sequences suffer from severe artefacts due to finite pulse lengths. In octadecasil, a spinning frequency of 14 kHz is shown to be necessary for an effective suppression of 19F–19F spin diffusion. The influences of experimental missettings and radiofrequency (RF) field inhomogeneity are taken into account. 相似文献
62.
63.
Wenqi Zeng Tammy Gillis Michael Hakky Luc Djoussé Richard H Myers Marcy E MacDonald James F Gusella 《BMC neuroscience》2006,7(1):62-9
Background
In Huntington's disease (HD), age at neurological onset is inversely correlated with the length of the CAG trinucleotide repeat mutation, but can be modified by genetic factors beyond the HD gene. Association of a relatively infrequent 16 TAA allele of a trinucleotide repeat polymorphism in the GRIK2 3'UTR with earlier than expected age at neurological onset has been suggested to reflect linkage disequilibrium with a functional polymorphism in GRIK2 or an adjacent gene. 相似文献64.
Mounir Bennoune Mohammed Lemou Luc Mieussens 《Journal of computational physics》2008,227(8):3781-3803
In this paper, we develop a numerical method to solve Boltzmann like equations of kinetic theory which is able to capture the compressible Navier–Stokes dynamics at small Knudsen numbers. Our approach is based on the micro/macro decomposition technique, which applies to general collision operators. This decomposition is performed in all the phase space and leads to an equivalent formulation of the Boltzmann (or BGK) equation that couples a kinetic equation with macroscopic ones. This new formulation is then discretized with a semi-implicit time scheme combined with a staggered grid space discretization. Finally, several numerical tests are presented in order to illustrate the efficiency of our approach. Incidentally, we also introduce in this paper a modification of a standard splitting method that allows to preserve the compressible Navier–Stokes asymptotics in the case of the simplified BGK model. Up to our knowledge, this property is not known for general collision operators. 相似文献
65.
Dr. David Tejedor Samuel Delgado-Hernández Lucía Colella Dr. Fernando García-Tellado 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(66):15046-15049
A universal, practical and scalable organocatalytic hydrocyanation manifold to provide β-substituted acrylonitriles bearing an electron-withdrawing functionality has been implemented. The catalytic manifold operates under the reactivity generation principle “a good nucleophile generates a strong base”, and it uses 1,4-diazabicyclo[2.2.2]octane (DABCO) as the catalyst, activated terminal alkynes as substrates and acetone cyanohydrin as the cyanide source. The acrylonitriles obtained as E,Z mixtures are straightforwardly resolved by simple flash chromatography delivering the pure isomers in preparative amounts. 相似文献
66.
Charlotte Menager Nathanaël Guigo Luc Vincent Nicolas Sbirrazzuoli 《Journal of polymer science. Part A, Polymer chemistry》2020,58(12):1717-1727
The curing of epoxidized linseed oil (ELO) with three different bio-based dicarboxylic acids (sebacic acid, suberic acid, and succinic acid) has been investigated. No accelerators or catalysts were used and the resulting thermosets are 100% bio-based. Structural investigations of the three crosslinked ELO resins were made using FTIR spectroscopy and TMA, that is, tensile tests, TGA, and DMA. As evidenced by FTIR measurements ELO and dicarboxylic acids reacts but no major differences can be distinguished between the dicarboxylic acids. Non-isothermal curing has been conducted by rheological and DSC measurements. Advanced isoconversional analysis applied to DSC data in association with the complex viscosity variations gives new insights into the polymerization mechanism. The length of dicarboxylic acid carbon chain modifies the reaction rate. Then, a correlation between reaction rate, activation energy, pre-exponential factors, polymerization mechanism, and change in rate-limiting step was shown. DMA and tensile tests highlight the relationship between the carbon chain length, reactivity, and thermomechanical properties. The use of succinic acid allows reaching a higher Tg and thermal stability. 相似文献
67.
Dr. Silvia Castro-Fernández Carlos M. Cruz Dr. Inês F. A. Mariz Dr. Irene R. Márquez Vicente G. Jiménez Lucía Palomino-Ruiz Prof. Juan M. Cuerva Dr. Ermelinda Maçôas Dr. Araceli G. Campaña 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(18):7205-7211
A new family of distorted ribbon-shaped nanographenes was designed, synthesized, and their optical and electrochemical properties were evaluated, pointing out an unprecedented correlation between their structural characteristics and the two-photon absorption (TPA) responses and electrochemical band gaps. Three nanographene ribbons have been prepared: a seven-membered-ring-containing nanographene presenting a tropone moiety at the edge, its full-carbon analogue, and a purely hexagonal one. We have found that the TPA cross-sections and the electrochemical band gaps of the seven-membered-ring-containing compounds are higher and lower, respectively, than those of the fully hexagonal polycyclic aromatic hydrocarbon (PAH). Interestingly, the inclusion of additional curvature has a positive effect in terms of non-linear optical properties of those ribbons. 相似文献
68.
Tania Merhi Alban Jonchère Dr. Luc Girard Dr. Olivier Diat Miquel Nuez Prof. Clara Viñas Dr. Pierre Bauduin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(61):13935-13947
Metalla-bis-dicarbollides, such as the cobalta-bis-dicarbollide (COSAN) anion [Co(C2B9H11)2]−, have attracted much attention in biology but a deep understanding of their interactions with cell components is still missing. For this purpose, we studied the interactions of COSAN with the glucose moiety, which is ubiquitous at biological interfaces. Octyl-glucopyranoside surfactant (C8G1) was chosen as a model as it self-assembles in water and creates a hydrated glucose-covered interface. At low COSAN content and below the critical micellar concentration (CMC) of C8G1, COSAN binds to C8G1 monomers through the hydrophobic effect. Above the CMC of C8G1, COSAN adsorbs onto C8G1 micelles through the superchaotropic effect. At high COSAN concentrations, COSAN disrupts C8G1 micelles and the assemblies become similar to COSAN micelles but with a small amount of solubilized C8G1. Therefore, COSAN binds in a versatile way to C8G1 through either the hydrophobic or superchaotropic effect depending on their relative concentrations. 相似文献
69.
70.
Daniel Arnaudon Jean Avan Luc Frappat Eric Ragoucy Junichi Shiraishi 《Annales Henri Poincare》2006,7(7-8):1327-1349
From the defining exchange relations of the
elliptic quantum algebra, we construct subalgebras which can be characterized as q-deformed WN algebras. The consistency conditions relating the parameters p, q, N and the central charge c are shown to be related to the singularity structure of the functional coefficients defining the exchange relations of specific
vertex operators representations of
available when N = 2.
Communicated by Petr Kulish
Submitted: January 13, 2006; Accepted: March 6, 2006
Dedicated to our friend Daniel Arnaudon 相似文献