K型区间删失数据下参数的置信限

基于K型区间删失数据,利用样本空间排序法给出参数优良的置信下限和计算置信下限的递推公式.     

Degenerate cascade fluorescence: Optical spectral-line narrowing via a single microwave cavity

For a three-level atom, two nondegenerate(even microwave and optical) electric dipole transitions are usually allowed; for either of these, the fluorescence spectra are well-described in terms of spontaneous transitions from a triplet of dressed sublevels to an adjacent lower-lying triplet. When the three dressed sublevels are equally spaced from each other, a remarkable feature known as degenerate cascade fluorescence takes place, which displays a five-peaked structure. We show that a single cavity can make all the spectral lines extremely narrow, whether they arise from cavity-coupled or cavity-free transitions. This effect is based on intrinsic cascade lasing feedback and makes it possible to use a single microwave cavity(even a bad cavity) to narrow the spectral lines in the optical frequency regime.     

Chaotic behavior of a stack of intrinsic Josephson junctions at the transition to branching for overcritical currents

Phase dynamics of a stack of coupled intrinsic Josephson junctions was investigated in the framework of capacitively coupled Josephson junctions with diffusion current model. We study the transition from the current-voltage characteristic specific to Josephson junctions arrays with small dissipation and weak coupling between the junctions to the arrays with strong coupling between the junctions and high dissipation. Low dissipative arrays of Josephson junctions are characterized by the absence of branching for overcritical currents which appears for highly dissipative arrays. Described branching appears due to charging on the superconducting layers and charge traveling waves generation. Arrays of Josephson junctions with intermediate values of coupling and dissipation parameters are characterized by the chaotic behavior, confirmed by positive Lyapunov exponent, and branching on the current voltage characteristic for both sub- and overcritical currents.     

含NO_4五齿配体的一维铜配位聚合物的合成、晶体结构与生物活性(英文)

利用邻氧乙酸苯甲醛与水杨酰肼合成了五齿配体Schiff碱H2L及其一维链状聚合物[(CuL)DMSO]n。产物经元素分析、红外、差热-热重分析及X-射线单晶结构分析等表征。在配位聚合物中Cu(Ⅱ)与配体的羰基氧、亚胺基氮、醚氧基氧及羧基氧配位形成一个O2N2平面,进一步被另一个配体的羧基氧桥联而形成一维配位聚合物。选取6种真菌对配体及其Cu(Ⅱ)配合物进行了抗真菌活性测试,测试结果表明配体及配合物均表现出了一定抗真菌活性。     

para-Sulfonatocalix[6]arene-modified silver nanoparticles electrodeposited on glassy carbon electrode: Preparation and electrochemical sensing of methyl parathion

In this paper, a new electrochemical sensor, based on modified silver nanoparticles, was fabricated using one-step electrodeposition approach. The para-sulfonatocalix[6]arene-modified silver nanoparticles coated on glassy carbon electrode (pSC₆-Ag NPs/GCE) was characterized by attenuated total reflection IR spectroscopy (ATR-IR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), etc. The pSC₆ as the host are highly efficient to capture organophosphates (OPs), which dramatically facilitates the enrichment of nitroaromatic OPs onto the electrochemical sensor surface. The combination of the host-guest supramolecular structure and the excellent electrochemical catalytic activities of the pSC₆-Ag NPs/GCE provides a fast, simple, and sensitive electrochemical method for detecting nitroaromatic OPs. In this work, methyl parathion (MP) was used as a nitroaromatic OP model for testing the proposed sensor. In comparison with Ag NPs-modified electrode, the cathodic peak current of MP was amplified significantly. Differential pulse voltammetry was used for the simultaneous determination of MP. Under optimum conditions, the current increased linearly with the increasing concentration of MP in the range of 0.01-80 μM, with a detection limit of 4.0 nM (S/N = 3). The fabrication reproducibility and stability of the sensor is better than that of enzyme-based electrodes. The possible underlying mechanism is discussed.     

Dispersive liquid-liquid microextraction based on the solidification of floating organic droplet for the determination of polychlorinated biphenyls in aqueous samples

In the proposed method, an extraction solvent with a lower toxicity and density than the solvents typically used in dispersive liquid-liquid microextraction was used to extract seven polychlorinated biphenyls (PCBs) from aqueous samples. Due to the density and melting point of the extraction solvent, the extract which forms a layer on top of aqueous sample can be collected by solidifying it at low temperatures, which form a layer on top of the aqueous sample. Furthermore, the solidified phase can be easily removed from the aqueous phase. Based on preliminary studies, 1-undecanol was selected as the extraction solvent, and a series of parameters that affect the extraction efficiency were systematically investigated. Under the optimized conditions, enrichment factors for PCBs ranged between 494 and 606. Based on a signal-to-noise ratio of 3, the limit of detection for the method ranged between 3.3 and 5.4 ng L⁻¹. Good linearity, reproducibility and recovery were also obtained.     

Preparation of anionic phosphine ligands in situ for the palladium-catalyzed Buchwald/Hartwig amination reactions of aryl halides

2-Phenylindenyl phosphine ligand can be changed into anionic phosphine ligand in situ and utilized in the palladium-catalyzed Buchwald/Hartwig amination reactions in DME, providing good to excellent yields of amination products from aryl chlorides, bromides and iodides. ³¹P NMR studies show that the resonance for the anionic phosphine appeared between those of the (2-phenylindenyl)-dicyclohexyl phosphonium salt and (2-phenylindenyl)dicyclohexylphosphine. The calculated results were consistent with the experimental results.     

Determination of silver(I) ion in water samples by graphite furnace atomic absorption spectrometry after preconcentration with dispersive liquid-liquid microextraction

A method was developed for the determination of silver ion (Ag) by combining dispersive liquid-liquid microextraction preconcentration with graphite furnace atomic absorption spectrometry. Diethyldithiocarbamate was used as a chelating agent, and carbon tetrachloride and methanol as extraction and dispersive solvent. Factors influencing the extraction efficiency of Ag and its subsequent determination were studied and optimized. The detection limit is 12 ng L^?1 (3 s) with an enrichment factor of 132, and the relative standard deviation is 3.5% (n?=?7, at 1.0 ng mL^?1). The method was successfully applied to the determination of trace amounts of Ag in water samples.     

Application of DLLME Based on the Solidification of Floating Organic Droplets for the Determination of Dinitrobenzenes in Aqueous Samples

Dispersive liquid–liquid microextraction (DLLME) based on the solidification of floating organic droplets (DLLME-SFO) combined with gas chromatography-electron-capture detection (GC–ECD) has been developed for extraction and analysis of three dinitrobenzenes. The extraction conditions including extraction solvent, disperser solvent, extraction time, salt effect and temperature were investigated and optimized systematically. The limits of detection were 0.019 μg L^?1 for 1,4-dinitrobenzene, 0.079 μg L^?1 for 1,3-dinitrobenzene and 0.034 μg L^?1 for 1,2-dinitrobenzene. Moreover, it offered good repeatability and high recovery. This method was successfully applied to monitor DNBs in different water samples.     

Synthesis and biological activity of novel phenyltriazolinone derivatives

Phenyltriazolinones are one of the most important classes of herbicides targeting the protoporphyrinogen oxidase enzyme. A series of triazolinone derivatives containing a strobilurin pharmacophore were designed and synthesized with the aim of discovering new phenyltriazolinone analogues with high activity. The herbicidal activity of the synthesized compounds was assayed and some of the test compounds displayed moderate herbicidal activity at 150 g ai/ha.