Search results for "coupling [Lambda(1520)]"

Nickel‐Catalyzed C(sp2)−C(sp3) Kumada Cross‐Coupling of Aryl Tosylates with Alkyl Grignard Reagents

2019

Aryl tosylates are an attractive class of electrophiles for cross‐coupling reactions due to ease of synthesis, low price, and the employment of C−O electrophiles, however, the reactivity of aryl tosylates is low. Herein, we report the Ni‐catalyzed C(sp2)−C(sp3) Kumada cross‐coupling of aryl tosylates with primary and secondary alkyl Grignard reagents. The method delivers valuable alkyl arenes by cross‐coupling with challenging alkyl organometallics possessing β‐hydrogens that are prone to β‐hydride elimination and homo‐coupling. The reaction is catalyzed by an air‐ and moisture stable‐Ni(II) precatalyst. A broad range of electronically‐varied aryl tosylates, including bis‐tosylates, underwe…

Synthesis of Mammalian Gonadoliberin Analogs with the N-terminal glutamine or glutamine or glutamic acid

1991

Synthesis of two mammalian gonadoliberin analogs, [Gln1]GnRH and [Glu1]GnRH, in solution by the peptide segment coupling of the [(2 + 4) + 4] type has been described.

Iron-Catalyzed C(sp2)-C(sp3) Cross-Coupling of Alkyl Grignard Reagents with Polyaromatic Tosylates

2017

Synthesis of brominated tetrathiafulvalenes via phosphite-mediated cross-coupling

2010

The synthesis of polybrominated tetrathiafulvalenes (TTF-Brn, 2-4) containing 2-4 bromine atoms via phosphite-mediated cross-coupling of bromo-substituted 1,3-dithiole-2-thiones and 1,3-dithiole-2-ones is reported. © 2010 Elsevier B.V.

Coherent Electronic Coupling versus Localization in Individual Molecular Dimers

2004

International audience; The electronic excitation transfer and coherent electronic coupling strength were investigated in molecular dimers by spectrally resolved confocal fluorescence spectroscopy. The direct probe of electronic coupling strength distribution was possible due to static disorder in polymer host by single molecule measurements. The dimers with delocalized excitation were also found in comparison to emission originated from localized states. The delocalized and localized state transitions were observed for dimers which were attributed to structural fluctuations of guest-host system.

Ferroelectric LC-elastomers

1997

Ferroelectric liquid crystalline elastomers combine the rubber elasticity of polymer networks with liquid crystalline phases and ferroelectric ordering. Ferroelectric switching leads therefore to a deformation of the polymer network and an elastic stress. The coupling between both effccts can be varied by changing the topology of the netpoints.

Complete in-plane elastic characterisation under tensile tests of angle-ply laminates composed of polymer-matrix layers

2002

In this paper we present a new strategy to completely characterise the in-plane elastic properties of a large range of angle-ply laminates using only unidirectional tests. We consider laminates having the same number of identical plies in the α and – α directions. This new method uses some preceding results found by Verchery for orthotropic laminates, namely the conditions of existence of a specific direction ω, in which the shear-extension coupling is null. The characterisation of the laminate is then made using the results of three tensile tests: two in the orthotropy axes, and the third one in the ω direction, in order to have always a pure one-dimensional state of stress. We show that …

Reduction of the glass transition temperature in polymer films: A molecular-dynamics study

2001

We present results of molecular dynamics (MD) simulations for a non-entangled polymer melt confined between two completely smooth and repulsive walls, interacting with inner particles via the potential $U_{\rm wall}\myeq (\sigma/z)^9$, where $z \myeq |z_{\rm particle}-z_{\rm wall}|$ and $\sigma$ is (roughly) the monomer diameter. The influence of this confinement on the dynamic behavior of the melt is studied for various film thicknesses (wall-to-wall separations) $D$, ranging from about 3 to about 14 times the bulk radius of gyration. A comparison of the mean-square displacements in the film and in the bulk shows an acceleration of the dynamics due to the presence of the walls. %Consistent…

Electron-relaxation-mode interaction in BaTiO3:Nb.

1992

Dielectric relaxation was previously reported in ${\mathrm{BaTiO}}_{3}$ and ${\mathrm{BaTiO}}_{3}$:Fe single crystals at radio frequencies [M. Maglione et al., Phys. Rev. B 40, 11 441 (1989)]. We have measured the dielectric dispersion in four ${\mathrm{BaTiO}}_{3}$:Nb samples (${\mathit{x}}_{\mathrm{Nb}}$0.3 at. %) as a function of frequency (10f${10}^{9}$ Hz) and temperature (20T450 K). The electronic conductivity of ${\mathrm{BaTiO}}_{3}$:Nb enhances drastically the relaxation step at all temperatures. In the rhombohedral phase of ${\mathrm{BaTiO}}_{3}$:Nb (T180 K), an unusual slowing down of the relaxation motion is measured. The relaxation time increases to more than ${10}^{\mathrm{\en…

Photoaffinity labeling of the coupling factor 1 from the thermophilic bacterum PS3 by 8-azido ATP

1984

AbstractTo localize the nucleotide binding sites of the F1ATPase (TF1) from the thermophilic bacterium PS3 we have used 14C-labeled 8-azido ATP (8-N3ATP) as photoaffmity label. 8-N3ATP is hydrolyzed by the F,ATPase in the absence of ultraviolet light. Irradiation by ultraviolet light of the enzyme in the presence of 8-N3ATP results in reduction of ATPase activity and in preferential nucleotide specific labeling of the α subunits (0.8–0.9 mol 8-N3ATP/TF1,α:β = 4:1). Inactivation and labeling do not depend on the presence of Mg2+. Both effects decrease upon addition of various nucleotide di- or triphosphates.