Transient dynamics of an adiabatic NEMS

This paper is focused on the transient dynamics of an adiabatic nano‐electromechanical system (NEMS), consisting of a nano‐mechanical oscillator coupled to a quantum dot. By numerically solving the nonlinear stochastic differential equation governing the oscillator, the time evolution of the oscillator position, of the dot occupation number and of the current are studied. Different parameter settings are studied where the system exhibits bi‐stable, tri‐stable or mono‐stable behavior on a finite‐time horizon. It is shown that, after a typically long transient, the system under investigation exhibits no hysteretic behavior and that a unique steady state is reached, independently of the initial conditions. The transient dynamics is marked out by one or two well separated characteristic times, depending on the considered case (i.e., mono‐ or multi‐stable). These times are evaluated for a dot on‐resonance or off‐resonance. It turns out that the characteristic time scales are long in comparison to the period of the uncoupled oscillator, particularly at low bias, suggesting that the predicted transient dynamics may be observed in state‐of‐the‐art experimental setups.

     

Asymmetric Synthesis of Highly Enantiomerically Enriched (S)(-)-β-Bisabolene

(S)-β-Bisabolene, (S)-1, was synthetized by a synthetic route in which (S)-4-methyl-3-cyclohexene carboxylic acid, (S)-10, which was the key intermediate, was prepared via a highly diastereoselective TiCl₄-catalyzed Diels-Alder reaction between isoprene and the acrylate of commercial (R)-pantolactone, followed by hydrolysis. Compound (S)-10 was then converted into ketone (S)-13 using two different procedures. The best one of these, as regards the degree of stereospecificity, involved the reaction of (S)-10 with 2 equiv of 4-methyl-3-penten-1-yllithium, 14, in the presence of CeCl₃, and gave (S)-13 having ca. 84% ee. The Zr-promoted methylenation of this ketone afforded highly enantiomerically enriched (S)-1.     

Chiral bidiaziridines by a two-step domino aziridination of meso-α-diimines

Chiral racemic α-diimines, tested in aziridination reactions with NsONHCO₂Et, for the first time led to the synthesis of (±)-bidiaziridines, stereoselectively derived from the corresponding meso (E-s-trans-E)-α-diimines. Moreover, a minor bidiaziridine isomer, probably a meso form that was lost under classical work-up conditions, can be obtained by adding water to the crude mixtures at the end of amination reactions. The results definitively prove that the imine aziridination by carbamates is a two-step domino process. The structures of the compounds were determined using 2D NMR on purified bidiaziridines.     

Application of modal analysis methods to the design of wireless power transfer systems

Meccanica - Wireless recharge of electric vehicles is an important field of research. Design of inductive power transfer systems involves the optimization of resonant coils coupled through mutually...     

Superfluidity and quantum melting of p-H2 clusters

Structural and superfluid properties of p-H2 clusters of size up to N=40 molecules, are studied at low temperature (0.5 K相似文献   

The adsorption of a substituted benzene,the ethynyl-trifluoro-toluene on Si(100)-2 × 1

The adsorption of 3-ethynyl-trifluoro-toluene (ETFT) on Si(100)-2 × 1 surface in ultra high vacuum is studied in the low coverage regime, through a joint experimental and theoretical approach. The STM images of both filled and empty states revealed few distinct adsorption configurations. On the basis of Density Functional Theory (DFT) calculations the STM images were simulated and three main adsorption configurations were identified, with a predominance of di-sigma bonded species that leave the benzene ring unreacted. A discussion of the reactivity of the reconstructed silicon surface towards benzene derivatives is proposed by comparing the adsorption of ETFT close related molecules, like styrene and phenylacetylene.     

Automorphisms of hyperbolic domains inR n

The main result of this paper is a fixed-point theorem for projective automorphisms of a bounded strongly convex domain inR ⁿ . Several corollaries and applications are derived, especially on the dimension of the full automorphism group in the smooth case.     

Aromatic compounds produced by endophytic fungi isolated from red alga Asparagopsis taxiformis - Falkenbergia stage

Endophytic fungi were isolated from red alga Asparagopsis taxiformis - Falkenbergia stage, collected from the Brazilian coast, and were identified as Annulohypoxylon stygium (AT-03) and A. yungensis (AT-06) based on their macro/micromorphological and molecular features. Bioassay-guided fractionation of the EtOAc extract from laboratory cultures of both strains yielded known compounds pyrogallol from A. stygium, (3R)-scytalone and (3R,4R)-4-hydroxy-scytalone from A. yungensis. Pyrogallol was active against methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli strains. An inactive fraction from A. stygium afforded two additional compounds, (3R,4R)-3,4,5-trihydroxy-1-tetralone and tyrosol. Optically active compounds had their stereochemistry determined by circular dichroism (CD) spectroscopy.     

Nonlinear asset-price dynamics and stabilization policies

Nonlinear Dynamics - We first present a brief review of nonlinear asset-pricing models and contributions in which such models have been used as benchmarks to evaluate the effectiveness of a number...