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271.
The photoelectron spectra (PES) of anions of uracil-glycine and uracil-phenylalanine complexes reveal broad features with maxima at 1.8 and 2.0 eV. The results of ab initio density functional B3LYP and second order M?ller-Plesset theory calculations indicate that the excess electron occupies a π* orbital localized on uracil. The excess electron attachment to the complex can induce a barrier-free proton transfer (BFPT) from the carboxylic group of glycine to the O8 atom of uracil. As a result, the four most stable structures of the anion of uracil-glycine complex can be characterized as the neutral radical of hydrogenated uracil solvated by the anion of deprotonated glycine. The similarity between the PES spectra for the uracil complexes with glycine and phenylalanine suggests that the BFPT is also operative in the case of the latter anionic species. The BFPT to the O8 atom of uracil may be related to the damage of nucleic acid bases by low energy electrons because the O8 atom is involved in a hydrogen bond with adenine in the standard Watson-Crick pairing scheme. Received 6 April 2002 Published online 13 September 2002  相似文献   
272.
A method of controlling global stochasticity in Hamiltonian systems by applying nonlinear perturbation is proposed. With the well-known standard map we demonstrate that this control method can convert global stochasticity into regular motion in a wide chaotic region for arbitrary initial condition, in which the control signal remains very weak after a few kicks. The system in which chaos has been controlled approximates to the original Hamiltonian system, and this approach appears robust against small external noise. The mechanism underlying this high control efficiency is intuitively explained. Received 15 January 2002 Published online 6 June 2002  相似文献   
273.
It was found that a beta-fructofuranosidase produced by Microbacterium sp. H-1 has potent trans-beta-fructofuranosylation activity from sucrose (donor). By means of this enzyme system, rebaudioside A (RA), the second major sweet steviol glycoside of the leaves of Stevia rebaudiana, was subjected to transfructosylation, affording a mono-beta-fructofuranosylated product (RA-F) in a high yield. The structure of RA-F was elucidated as beta-D-fructofuranosyl-(2----6)-beta-D-glucopyranosyl ester of steviol-13-O-[beta-D-glucopyranosyl-(1----2)]- [beta-D-glucopyranosyl-(1----3)]-beta-D-glucopyranoside. Some improvement in the quality of sweetness was observed for RA-F.  相似文献   
274.
Dynamically obtained current/voltage curves of bilayer lipid membranes partitioning a solution of lipophilic ions are compared with the results of the type expected in a voltammetry experiment involving ionic transport across a liquid/liquid interface. Lipophilic ions yielding “voltammograms” analogous to reversible and irreversible voltammograms (in conventional electrochemical systems) are reported. Also reported are examples of ions which yield what may be analogous to a masked response, a phenomenon known in the literature of liquid/liquid interfaces. Although the behavior of the two systems is similar, there exist differences in the interpretation of the voltammograms and suggestions are offered for an energetic and mechanistic interpretation of the membrane voltammogram.  相似文献   
275.
276.
Barotropic FRW cosmologies are presented from the standpoint of nonrelativistic supersymmetry. First, we reduce the barotropic FRW system of differential equations to simple harmonic oscillator differential equations. Employing the factorization procedure, the solutions of the latter equations are divided into the two classes of bosonic (nonsingular) and fermionic (singular) cosmological solutions. We next introduce a coupling parameter denoted by K between the two classes of solutions and obtain barotropic cosmologies with dissipative features acting on the scale factors and spatial curvature of the universe. The K-extended FRW equations in comoving time are presented in explicit form in the low coupling regime. The standard barotropic FRW cosmologies correspond to the dissipationless limit K = 0.  相似文献   
277.
The yet unknown intermetallic phase La5Al3Ni2 was obtained by partially crystallizing amorphous La50Al25Ni25 at 550 K (further heating above 600 K leads to irreversible disappearance of this phase), and its crystal structure was determined from X‐ray powder diffraction data. The crystal structure of the La5Al3Ni2 phase constitutes a new structure type (Cmcm, a = 14.231Å, b = 6.914Å, c = 10.460Å, oC40) and is built from [Al3Ni2] chains surrounded by La atoms. In the ternary system La‐Al‐Ni La5Al3Ni2 is located on the section La50Al50−nNin (0 ≤ n ≤ 50) with the binary compounds LaAl and LaNi as end members. Strikingly, also the crystal structures of the end members can be conceived as chain structures with Al and Ni chains surrounded by La, respectively.  相似文献   
278.
279.
We use the spectral ballistic imaging technique to measure the impulse response of a Fabry–Pérot etalon with less than 0.2 ps temporal resolution. The results show excellent agreement with the theoretical predictions and negligible noise. Comparison to the Kramers–Kronig method along with its limitations is also presented. PACS 42.65.Re; 07.60.Ly; 42.30.Kq  相似文献   
280.
Current techniques of water wave visualization such as shadowgraphy and stereo photography are widely used but are deficient in many aspects. Refraction based visualization observes the bending of light as it traverses across a liquid-air interface. This work describes the continued development of techniques to measure the surface height of a liquid free surface. The method, Reference Image Topography, utilizes refraction of light at the free surface as a function of the local angle of that surface. Particle Image Velocimetry (PIV) software is used to evaluate apparent dislocations of the target image viewed through the free surface, which are approximately proportional to the surface angle. High-resolution images are presented of the dynamic surface topography for a point source and the shallow water flow around a vertical cylinder.  相似文献   
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