强流电子束泵浦XeCl准分子激光动力学模型

强流电子束泵浦XeCl准分子激光动力学模型由三部分组成,即电子束能量沉积的计算;电子温度、电子反应速率的计算和化学/激光动力学。这个模型可以准确地预报小信号增益、吸收等激光特征量的时间变化规律。 该模型是在文献[1]、[2]、[3]报导的动力学模型的基础上提出的。采用四阶龙格_库塔法在VAX—11/780机器上进行数值求解。 计算给出XeCl准分子激光反应过程中各种粒子浓度、小信号增益、吸收、输出光强、激发速率以及平均电子能量随时间的变化规律。计算结果表明本征效率是激发速率,电流密度和工作气体(Ne/Xe/HCl)的各分压比的函数。 该模型可为高功率准分子激光器的研制提供设计参数和最佳实验条件。     

Superconductivity,magnetic susceptibility and thermal relaxation in amorphous CuZr

From measurements of the superconducting transition temperature and valence magnetic susceptibility ξ_v, of amorphous Cu_100?xZr_x (30? x ? 80), we find that ln T_c varies as (ξ_v)^?1 implying that with changing x, T_c is controlled only by the electronic density of states. By contrast, thermal relaxation reduces T_c substantially, leaving ξ_v almost unaltered, implying that T_c is changed only by change in the effective electron-electron coupling.     

使用α粒子轰击天然镱靶制备~(178m2)Hf同质异能素及样品γ能谱分析

178m2Hf是一种长半衰期(T1/2=31 a)、高自旋态(Iπ=16+)的Hf同质异能素.利用四川大学CS-30回旋加速器产生的30 MeV,100μA的α束流轰击天然Yb靶,通过176Yb(α,2n)反应制备178m2Hf.采用高纯Ge探测器测量未提纯样品和放化分离后的样品的γ能谱,选取178m2Hf的426,495和574 keV三个特征峰,使用高斯双峰拟合方法解谱,确定了未提纯样品中178m2Hf的含量达到1012量级,提纯后的样品中178m2Hf含量为1011量级.还对靶中其他放射性杂质核素(175Hf,172Lu,172Hf,177Lu,173Lu)的含量进行了分析.     

Elliptic flow of transported and produced protons in Au+Au collisions with the UrQMD model

Within the framework of the UrQMD model, by tracing the number of initial quarks in protons, we study the elliptic flow of protons with 3, 2, 1, 0 initial quarks and anti-protons in Au+Au collisions at SNN~(1/2)= 7.7, 11.5, 39,200 GeV. The difference of elliptic flow between protons with 2, 1, 0 initial quarks and anti-protons is smaller than 0,or consistent with 0, respectively. The difference of elliptic flow between transported protons(with 3 initial quarks)and anti-protons is larger than 0 at 7.7, 11.5 and 39 GeV. This is in good agreement with the STAR results at 7.7 and 11.5 GeV, but overestimates the STAR results at 39 GeV. The yield of transported protons with 3 initial quarks is smaller than of protons with 2 and 1 initial quarks, and v_2 of all protons is much smaller than the STAR results. The observation of the v_2 difference of elliptic flow between transported protons and anti-protons in the UrQMD model partly explains the difference between protons and anti-protons observed in the Beam Energy Scan program at the Relativistic Heavy Ion Collider(RHIC).     

On proximality with Banach density one

Let (X,T)$(X,T)$ be a topological dynamical system. A pair of points (x,y)∈X²$(x,y)\in X^2$ is called Banach proximal if for any ε>0$\epsilon >0$, the set {n∈_Z+:d(Tⁿx,Tⁿy)<ε}$\{n\in {\mathbb{Z}}_{+}:d(T^{n}x,T^{n}y)<\epsilon \}$ has Banach density one. We study the structure of the Banach proximal relation. A useful tool is the notion of the support of a topological dynamical system. We show that a dynamical system is strongly proximal if and only if every pair in X²$X^2$ is Banach proximal. A subset S of X is Banach scrambled if every two distinct points in S form a Banach proximal pair but not asymptotic. We construct a dynamical system with the whole space being a Banach scrambled set. Even though the Banach proximal relation of the full shift is of first category, it has a dense Mycielski invariant Banach scrambled set. We also show that for an interval map it is Li–Yorke chaotic if and only if it has a Cantor Banach scrambled set.     

Palladium complexes with bis(diphenylphosphinomethyl)amino ligands and their application as catalysts for the Heck reaction

Aminomethylphosphine (P–C–N) type ligands, (Ph₂PCH₂)₂NR R = –(CH₂)₃Si(OEt₃)₃ or –CH₂CH₂OH, and their Pd(II) complexes have been synthesized. All the compounds were characterized by ¹H-, ³¹P-NMR, and elemental analysis. The complexes are proposed to have a square planar geometry. They were investigated as catalysts for the Heck reaction of aryl halides (I, Br, Cl) with methyl acrylate. Both complexes showed high activity to give methyl cinnamate in good yields, with the best turnover numbers found for [PdCl₂(Ph₂PCH₂)₂N(CH₂)₃Si(OEt)₃].     

Green and high efficient synthesis of triaza‐benzo[b]fluoren‐6‐one derivatives in water under microwave irradiation

Triaza‐benzo[b]fluoren‐6‐one derivatives were synthesized via the three‐component reaction of aldehyde, cyclohexane‐1,3‐dione compound and 2‐aminobenzimidazole in water under microwave irradiation. The new protocol has the advantages of excellent yield, low cost, reduced environment impact, wide scope and convenient procedure.     

Improved binary PSO for feature selection using gene expression data

Gene expression profiles, which represent the state of a cell at a molecular level, have great potential as a medical diagnosis tool. Compared to the number of genes involved, available training data sets generally have a fairly small sample size in cancer type classification. These training data limitations constitute a challenge to certain classification methodologies. A reliable selection method for genes relevant for sample classification is needed in order to speed up the processing rate, decrease the predictive error rate, and to avoid incomprehensibility due to the large number of genes investigated. Improved binary particle swarm optimization (IBPSO) is used in this study to implement feature selection, and the K-nearest neighbor (K-NN) method serves as an evaluator of the IBPSO for gene expression data classification problems. Experimental results show that this method effectively simplifies feature selection and reduces the total number of features needed. The classification accuracy obtained by the proposed method has the highest classification accuracy in nine of the 11 gene expression data test problems, and is comparative to the classification accuracy of the two other test problems, as compared to the best results previously published.     

Application of polarity switching in the identification of the metabolites of RO9237

Polarity switching mass spectrometry is an efficient way to collect structural data on drug metabolites. The value of this approach is illustrated with the in vitro metabolism of RO9237. Metabolites are identified by positive and negative electrospray ionization (ESI) full scan mass spectrometry, MS/MS and MS(3) using unlabelled and (14)C-radiolabelled versions of the drug. Comparison of the relative detectability of these metabolites by +ESI and -ESI shows that neither ESI mode is universal. It is advantageous to screen for metabolites using both positive and negative ionization modes. This is especially true for phase II metabolism which tends to make molecules more polar and often more acidic. Identification of phase II metabolites also benefits greatly from MS(3) experiments because the conjugating groups typically are cleaved in MS/MS and information on the core structure is only obtained in MS(3). A special case of phase II metabolism is the generation of glutathione (GSH) conjugates from reactive metabolites. The detection of GSH conjugates also benefits from generating both positive and negative ESI mass spectral data.     

(±) Gancochlearols A and B: cytotoxic and COX-2 inhibitory meroterpenoids from Ganoderma cochlear

Abstract

(+)- and (?)-gancochlearols A (1) and B (2), two pairs of dimeric mertoterpenoid enantiomers were isolated from the fruiting bodies of Ganoderma cochlear. Their structures were identified by spectroscopic methods. Biological assessments show that the enantiomers of 1 and 2 are cytotoxic against three human cancer cell lines (A549, K562, Huh-7) and could inhibit COX-2 expression with IC₅₀ values less than 10?μM.