Unsteady axisymmetric stagnation flow on a circular cylinder

Unsteady, axisymmetric stagnation flow about a circular cylinderis examined when the far-field flow is a periodic function oftime with a fixed time average and an oscillatory part of prescribedamplitude and frequency. Solutions are computed for arbitraryvalues of the Reynolds number, quantifying the effects of surfacecurvature, and a frequency parameter based on the period ofthe far-field flow. It is found that solutions remain regularand periodic provided that the far-field amplitude lies belowa critical value. Above this value, solutions terminate in afinite-time singularity. The blow-up time is delayed by increasingthe curvature of the surface. These results are corroboratedby asymptotic predictions valid in the limits of small and largeamplitude and frequency. For large Reynolds number, the problemreduces to the two-dimensional stagnation-point flow againsta plane wall studied by previous authors.     

Polyethylene glycol matrix reduces the rates of photochemical and thermal release of nitric oxide from S-nitroso-N-acetylcysteine

S -nitrosothiols have many biological activities and may act as nitric oxide (NO) carriers and donors, prolonging NO half-life in vivo. In spite of their great potential as therapeutic agents, most S -nitrosothiols are too unstable to isolate. We have shown that the S -nitroso adduct of N -acetylcysteine (SNAC) can be synthesized directly in aqueous and polyethylene glycol (PEG) 400 matrix by using a reactive gaseous (NO/O₂) mixture. Spectral monitoring of the S–N bond cleavage showed that SNAC, synthesized by this method, is relatively stable in nonbuf-fered aqueous solution at 25°C in the dark and that its stability is greatly increased in PEG matrix, resulting in a 28-fold decrease in its initial rate of thermal decomposition. Irradiation with UV light (λ= 333 nm) accelerated the rate of decomposition of SNAC to NO in both matrices, indicating that SNAC may find use for the photogeneration of NO. The quantum yield for SNAC decomposition decreased from 0.65 ± 0.15 in aqueous solution to 0.047 ± 0.005 in PEG 400 matrix. This increased stability in PEG matrix was assigned to a cage effect promoted by the PEG microenvironment that increases the rate of geminated radical pair recombination in the homolytic S–N bond cleavage process. This effect allowed for the storage of SNAC in PEG at −20°C in the dark for more than 10 weeks with negligible decomposition. Such stabilization may represent a viable option for the synthesis, storage and handling of S -nitrosothiol solutions for biomedical applications.     

Electron delocalization in linearly pi-conjugated systems: a concept for quantitative analysis

Donor- and/or acceptor-substituted pi-conjugated systems represent an important class of compounds in organic chemistry. However, up to now, a general method to quantitatively address the efficiency of a conjugated path is still missing. In this work, a novel computational approach based on deletion energies and on second-order orbital interaction energies in a natural bond orbital (NBO) scheme is employed to quantitatively assess ("measure") delocalization energies. Moreover, the purpose of this work is to assess the efficiency of distinct pi-conjugated paths, that is, geminal, cis, and trans, as well as to predict the impact of substituents on a given backbone. This study is focused on various mono-, di-, tri-, and tetrasubstituted tetraethynylethenes (TEEs). These model systems are suitable for our analysis, because they offer distinct conjugation paths within the same molecule, and can also be substituted in multiple ways. Differences between conjugation paths, the effect of neighbor paths, and the impact of donor and acceptor substituents on the various paths are discussed.     

广义Bethe树上奇偶马尔可夫链场上的若干极限性质

通过构造两个非负鞅证明了一个强极限定理,然后把它应用到本文所定义的广义Bethe树上的奇偶马尔可夫链场上,从而获得了此马氏链场上的一类强极限定理.     

Through versus cross electron delocalization in polytriacetylene oligomers: a computational analysis.

Herein, we report a systematic theoretical investigation of the molecular and electronic properties of unsubstituted polytriacetylene (PTA) and iso-polytriacetylene (iso-PTA) oligomers, which are characterized by through and cross pi-conjugation pathways, respectively. The goal of the study is to compare through versus cross conjugation on the basis of the computed molecular geometries of the neutral, anionic, and cationic species, the electron affinities, ionization potentials, excitation energies, and nonlinear optical properties for oligomers up to the nonamer. Differences in the effective conjugation length are directly related to electron delocalization in cross- and through-conjugated pathways. As in the through-conjugated oligomers, that is, the PTAs, the frontier orbitals of the iso-PTA oligomers are delocalized along the entire carbon backbone, suggesting that pi-delocalization can extend through cross-linked carbon atoms. However, in contrast to the PTA oligomers, the bond lengths remain strictly constant and the reduction of the energy gap beyond the trimer is completely due to the correlation contribution. On the other hand, in the anions and cations, the bond lengths do change significantly with increasing chain length. Therefore, oxidation or reduction of the iso-PTA oligomer appears to switch on delocalization through cross-linked carbon atoms. Obviously, the effective conjugation length is specific and depends on the observable considered.     

Suppression of plasma turbulence during optimized shear configurations in JET

Correlation of density turbulence suppression and reduced plasma transport is observed in the internal transport barrier (ITB) region of JET tokamak discharges with optimized magnetic shear. The suppression occurs in two stages. First, low frequency turbulence and ion transport are reduced across the plasma core by a toroidal velocity shear generated by intense auxiliary heating. Then with the ITB formation, high frequency turbulence and electron transport are reduced locally within the steep pressure gradient region of the ITB.     

trans versus geminal electron delocalization in tetra- and diethynylethenes: a new method of analysis

trans-Diethynylethene [(E)-hex-3-ene-1,5-diyne (1 a)], geminal-diethynylethene [3-ethynyl-but-3-ene-1-yne (1 b)], and tetraethynylethene [3,4-diethynyl-hex-3-ene-1,5-diyne (2)] are flexible molecular building blocks for pi-conjugated polymers with interesting electronic and photonic properties. The type of functionalization, the length of the polymer chain, and the choice of pi-conjugation pattern, play a crucial role in determining the properties of these compounds. To rationalize the impact of the different delocalization pathways in the various types of isomers (trans or geminal) on the molecular and electronic structure, a detailed theoretical investigation is presented. We develop a method based on the natural bond orbital (NBO) analysis of Weinhold, which allows one to correlate electron delocalization with molecular and electronic structure observables. The method reveals that the difference between trans (or through) and geminal (or cross) conjugation is not only due to the vertical pi conjugation, but also to the in-plane sigma hyperconjugation. The method is used to correlate the changes in molecular and electronic observables, such as the bond lengths or the absorption frequencies, with the electronic structure of the compounds under investigation. Moreover, this method allows us to predict how a certain substituent will affect the molecular structure and the electronic properties of a given backbone.     

Antibacterial properties of composite UHMWPE/\mathrm {TiO}_{2-{\it x}} surfaces

Due to the diffusion of severe pathogens, everyday life is exposed to the risks of contracting severe diseases. For this reason, efficient antimicrobial surfaces are of paramount importance. In this work we present the first evidences of a new technique to obtain an antibacterial ultra high molecular weight polyethylene based on a non-stoichiometric, visible light responsive, titanium oxide coating. The coating was obtained through a process in which titanium ions, resulting from laser ablation of a corresponding target, were accelerated and implanted on the samples. The samples were tested against a Staphylococcus aureus strain, in order to assay their antimicrobial efficacy. Results show that this treatment strongly discourages bacterial colonization of the treated surfaces.     

Nuclear orbiting and anomalies in nuclear reactions

In this paper, we report our measurements of back-angle oxygen and carbon particle yields from ¹⁶O+⁸⁹Y, ¹²C+⁹³Nb reactions forming the same compound nucleus ¹⁰⁵Ag at the same excitation energy and spin distribution. We find anomalously large oxygen yield and entrance channel dependence at high excitation energies from ¹⁶O+⁸⁹Y reaction implying formation of a dinuclear orbiting complex. Possible connection between nuclear orbiting and fast fission is also discussed.