铷原子磁光阱中超冷等离子体的形成和演化

在铷原子的磁光阱中,通过光电离冷原子方法和稠密里德堡原子的自发演化方法产生了超冷等离子体。磁光阱中冷却并囚禁了10^7个原子,温度约为500μK,之后用一束脉冲激光将冷原子电离或者激发至高里德堡态,通过调节脉冲激光的能量控制离子数量或者里德堡原子的数量。利用延迟斜坡电场或脉冲电场引出超冷等离子体中的电子,对超冷等离子体的形成和演化进行了研究,并利用库仑势阱模型对实验结果进行了解释。实验结果表明,由于来自长寿命里德堡原子的贡献,里德堡原子自发演化形成的超冷等离子体的寿命比光电离形成的超冷等离子体的寿命长。     

Phosphate-Based Self-Immolative Linkers for the Delivery of Amine-Containing Drugs

Amine-containing drugs often show poor pharmacological properties, but these disadvantages can be overcome by using a prodrug approach involving self-immolative linkers. Accordingly, we designed l-lactate linkers as ideal candidates for amine delivery. Furthermore, we designed linkers bearing two different cargos (aniline and phenol) for preferential amine cargo release within 15 min. Since the linkers carrying secondary amine cargo showed high stability at physiological pH, we used our strategy to prepare phosphate-based prodrugs of the antibiotic Ciprofloxacin. Therefore, our study will facilitate the rational design of new and more effective drug delivery systems for amine-containing drugs.     

Role of gemini surfactants (m‐s‐m type; m = 16, s = 4–6) on the reaction of [Zn(II)‐Gly‐Phe]+ with ninhydrin

In the present paper, reaction of zinc‐glycylphenylalanine ([Zn(II)‐Gly‐Phe]⁺) with ninhydrin has been investigated in gemini (m‐s‐m type; m = 16, s = 4–6) surfactants at temperature (70 °C) and pH (5.0). Monitoring the appearance of product at 400 nm was used to follow the kinetics, spectrophotometrically. The order of the reaction with respect to [Zn(II)‐Gly‐Phe]⁺ was unity while with respect to [ninhydrin] was fractional. The reaction constants involved in the mechanism were obtained. In addition to the rate constant (k_Ψ) increase and leveling‐off regions are observed with the geminis, just like as seen with conventional surfactant hexadecyltrimethylammonium bromide (CTAB), the former produced a third region of increasing k_Ψ at higher concentrations. A close agreement between observed and calculated rate constants was found under varying experimental conditions. A suitable mechanism consistent with the experimental findings has been proposed. Copyright © 2014 John Wiley & Sons, Ltd.     

Priority-based parameter optimization strategy for reducing the effects of four-wave mixing on WDM system

In order to meet the ultra high speed and ultra long-haul transmission distance in wavelength division multiplexing (WDM) systems, the nonlinear impairment affecting the overall spectral efficiency and system performance should be minimized. This paper proposes a strategy to mitigate the four-wave mixing (FWM) effect in WDM system. The strategy determines the effect of both single and combined effects of second, third, and fourth optimization priority parameters such as fiber length, input power, dispersion, channel spacing, and effective area on FWM power. A comparison study was made under different types of optical fiber such as single-mode fiber (SMF), dispersion shifted fiber, non-zero dispersion fiber, and non-zero dispersion shifted fiber. In addition, the system performance in term of bit-error-rate was calculated in the case of single priority (impact of effective area) and combined priority (impact of effective area, input power, fiber length and channel spacing). The results show that the FWM effect was reduced based on the transmission parameters order of optimization, i.e., priority selection proposed. Moreover, the results indicated that increasing sequentially the effective area, fiber length; channel spacing and decreasing the input power provide the most significant sequence in suppressing the effects of FWM. This priority sequence brought the suppression ratio to approximately 26.3% in SMF, which suppressed the FWM effects up to −50 dBm. In term of BER; the combined priority introduces improvement in BER of 2.31 × 10⁻²⁵ in comparison with single priority that has value of BER 4 × 10⁻¹⁴. Finally, this work suggests that the proposed priority-based parameter optimization strategy is an ideal solution for optimum performance of WDM system.     

基于高频雷达多普勒谱预测风向的一种新方法

通过高频雷达一阶多普勒谱与海上风向的关系, 提出了一种基于神经网络和多波束采样法相结合预测海面风向的新方法. 在神经网络不同输入、输出参数情况下对扩展因子为奇数时的仿真数据进行了风向预测, 并在扩展因子为偶数时结合多波束采样法进行风向预测, 消除了风向的模糊性. 通过预测数据和仿真数据对比, 发现两者符合较好. 从神经网络和多波束采样法相结合的预测结果中可以看出, 风向的误差大约为4°—6°, 风向扩展因子的平均误差为0.26, 为预测海面风场的研究提供一种新的思路和方法.     

Comparative analysis of photoluminescence and Raman enhancement by metal nanoparticles

We present a comparative study on the enhancement of photoluminescence and Raman processes by a single metal nanoparticle. Taking an analytical approach, we show the physics behind strikingly different orders of magnitude in enhancement that have been observed, provide fundamental explanation for not observing quenching of Raman processes, and outline the path to optimization of both photoluminescence and Raman enhancement.     

One-pot thioetherification of aryl halides with thiourea and benzyl bromide in water catalyzed by Cu-grafted furfural imine-functionalized mesoporous SBA-15

Surface functionalization of SBA-15 followed by its reaction with Cu(OAc)(2) has been carried out to develop a new Cu-grafted functionalized mesoporous material, which catalyzes one-pot three component coupling of different aryl halides with thiourea and benzyl bromide in aqueous medium to produce aryl thioethers in very good yields (80-88%).     

Recent trends in chiral separations on immobilized polysaccharides CSPs

Polysaccharide CSPs are recognized widely in chiral chromatography but the introduction of immobilized phases (Chiralpak IA, Chiralpak IB and Chiralpak IC columns) is a remarkable achievement. The immobilized CSPs can be used with organic, normal and reversed phase modes; even with prohibited solvents too (tetrahydrofuran, chlorofom, dichloromethane, acetone, 1,4-dioxane, ethylacetate, and certain other ethers). Their susceptibilities to work with a wide range of solvents have increased the range of applications including chiral recognition mechanisms. Besides, these are also useful for monitoring the progress of stereo-specific reactions; normally need prohibited solvents. The present review describes the various aspects of commercial available immobilized chiral columns. Attempts have been made to discuss immobilized polysaccharides CSPs, immobilized vs coated CSPs, comparison of immobilized CSPs, method development, optimization, chiral recognition mechanism and applications. The chiral recognition capabilities of commercial columns were in the order of Chiralpak IA > Chiralpak IB > Chiralpak IC columns; but complimentary to each other. Of course, these CSPs are not fully developed and need more advancements and applications. Definitely, the future of immobilized CSPs is quite better. Hopefully, in the coming years they will be the choice of the chromatographers for chiral separations in liquid chromatography.     

Comparative estimate of the efficiency of the sorption extraction of iodine from chloride solutions

The possibility of applying activated carbon and polymeric sorbents poly(4-vinylpyridine), polytrimethylsilylpropyne (PTMSP), bromo-substituted PNMSP (Br-PNMSP), poly(N-methyl-4-vinylpyridinium iodide) for the sorption recovery of iodine from a 0.5 M solution of sodium chloride is studied. The dependence of iodine sorption on the pH of solution, the amount of adsorbent, and the duration of contact between the solution and adsorbent is studied. The highest sorption capacity (G = 616.78 mg/g) is attained by using poly(N-methyl-4-vinylpyridinium iodide) anionite with the addition of iodine to form complex triiodide ions. The dynamics of iodine adsorption on poly(4-vinylpyridine) is described by a kinetic model of pseudosecond order. The composition and structure of the iodine compounds sorbed by polymers and activated carbon are studied by Raman spectroscopy (RS).     

Bis{(μ-acetato)[μ-bis(salicylidene)-1,3-propanediaminato]zinc(II)}zinc(II)

In the title linear trinuclear compound, [Zn{Zn(CH₃COO)(C₁₇H₁₆N₂O₂)}₂], the central Zn²⁺ ion, which is located on an inversion centre, has a distorted octahedral coordination involving four bridging O atoms from two N,N′-bis­(salicyl­idene)-1,3-propane­diaminate ligands in the equatorial plane and one O atom from each bridging acetate group in the axial positions. The coordination around the terminal Zn²⁺ ion is irregular square pyramidal, with two O and two N atoms of the ligand in the basal plane and one O atom from an acetate group in the apical position. The acetate bridges linking the central and terminal Zn²⁺ ions are mutually trans. The Zn⃛Zn distance is 3.0520 (8) Å. The relationship of this structure to that of [Zn{Cu(CH₃COO)(C₁₇H₁₆N₂O₂)}₂] is discussed.