COS Activation by Zr~＋ in the Gas Phase：A Case of Two-state Reactivity Process

To elucidate the mechanisms of Zr + reacting with COS,both the quartet and doublet potential energy surfaces (PESs) for reactions of Zr + (4 F,2 D) with COS in the gas phase have been investigated in detail by means of density functional method (B3LYP).To obtain more accurate results,the coupled cluster single-point calculations (CCSD(T)) using B3LYP optimized geometries were performed.For the C-O bond activation,the calculated results indicate that both the quartet and doublet states proceed via an insertion-elimination mechanism.For the C-S bond activation,the quartet reaction has an insertion-elimination mechanism,but the doublet reaction is a direct abstraction of the sulfur atom by Zr +.The C-S bond activation is found to be energetically more favorable than the C-O bond activation.It is found that the reaction of the 4 F gound state of Zr + to yield ZrO + is spin-forbidden (Zr + (4 F) + COS (1 Σ) → ZrO + (2) + CS (1 Σ)) and the crossing points were approximately determined.All the results have been compared with the existing experimental and theoretical data.     

非奇H矩阵的充分条件

文章通过引进一类具有非零元素链的矩阵,利用α对角占优矩阵性质,给出了一个新的非奇H矩阵的充分条件,扩大了非奇H矩阵的判定范围．     

毛细管电泳-联吡啶钌电化学发光法对血浆中丁卡因与普鲁卡因的同时测定

建立了毛细管电泳-电致化学发光同时测定丁卡因和普鲁卡因的新方法.考察了毛细管电泳流动相和检测池中磷酸盐缓冲液pH和浓度、进样时间和电压、分离电压和检测电位等对丁卡因和普鲁卡因的分离以及联吡啶钌电致化学发光检测的影响.基于循环伏安法考察了丁卡因和普鲁卡因的电化学行为与发光机理.在优化的实验条件下,丁卡因和普鲁卡因的标准曲线分别在6.6 ～265.6 μmol/L和0.7 ～219.0 μmol/L范围内呈良好的线性,检出限(S/N=3)分别为1.9 μmol/L和0.2 μmol/L.对23 μmol/L丁卡因和15 μmol/L普鲁卡因的标准溶液连续测定5次,迁移时间的相对标准偏差(RSD)分别为0.13%、0.16%,电化学法发光强度的RSD分别为3.7%和4.9%.该方法已成功用于血浆中丁卡因和普鲁卡因的同时检测,平均回收率均为94%,相对标准偏差低于4%.     

The Interaction of Peregrine Solitons

We theoretically investigate the interaction of two in-phase and out-of-phase Peregrine sofitons in a Kerr nonlinear medium, addressing both the cases of first- and second-order solitons. Upon adjusting the interval between the sofitons, their interactions exhibit different properties. If the interval is sufficiently large, two Peregrine sofitons will propagate individually and will not interact each other. However, if the interval is not very large, the Peregrine solitons will strongly interact and display varying behavior.     

Fourth-Order Spatial Correlation of Thermal Light

We investigate the fourth-order spatial correlation properties of pseudo-thermal light in the photon counting regime, and apply the Klyshko advanced-wave picture to describe the process of four-photon coincidence counting measurement. We deduce the theory of a proof-of-principle four-photon coincidence counting configuration, and find that if the four randomly radiated photons come from the same radiation area and are indistinguishable in principle, the fourth-order correlation of them is 24 times larger than that when four photons come from different radiation areas. In addition, we also show that the higher-order spatial correlation function can be decomposed into multiple lower-order correlation functions, and the contrast and visibility of low-order correlation peaks are less than those of higher orders, while the resolutions all are identical. This study may be useful for better understanding the four-photon interference and multi-channel correlation imaging.     

可允许集上的广义向量拟均衡问题

主要讨论可允许集上的广义向量拟均衡问题,推广L in的一些结果.     

1,2-二（二苯基膦）乙烷氯化钯(II)的合成及催化活性

以卤化钯（X=Cl、 Br、 I）为原料,乙腈为溶剂,与1,2-二（二苯基膦）乙烷反应,合成了1,2-二（二苯基膦）乙烷卤化钯[Pd(dppe)X₂, dppe=1,2-二（二苯基膦）乙烷],产率均高于96％,其结构经¹H NMR, XRD和元素分析确证。以Suzuki反应和Stille C—C偶联反应为模板反应,研究了Pd(dppe)Cl₂的催化活性。结果表明：Pd(dppe)Cl₂对2-氯噻吩和对甲氧基苯硼酸的Suzuki偶联反应、4,7-二氯苯并噻二唑核或其他含苯并噻二唑核的卤代芳烃与其他芳香核的锡试剂的Stille C—C偶联反应的催化转化率分别为80%~85%和52%~60%,催化活性优于四（三苯基膦）钯(70%~85%和43%~50%)。     

非自伴Sturm-Liouville算子的渐近迹

<正> 本文研究下列带一般两点边界条件的一维Schrodinger方程的特征值问题的渐近迹其中q(x)是[0,π]上的光滑复值函数,a_k,b_k是复常数. (E)的古典情形(Sturm-Liouville问题)的迹,自1953年以来,已引起国内外一系     

一个产生Bargmann势与N带势的三次系统

在位势与特征函数的一个代数约束:u=f(ψ)=-4〈Bψ,ψ〉下,KdV方程的Lax对被非线性化为一个三次系统和一个发展方程。二者自然相容:前者的解簇是后者决定的流的不变集,此外,三次系统的解ψ给出的u=f(ψ)满足驻定的KdV方程,在衰减情形与周期情形分别给出Bargmann势与N带势。     

SOME TRACE FORMULAS FOR THE SCHRDINGER EQUATION WITH ENERGY-DEPENDENT POTENTIAL

The importance of the inverse scattering problem for the Schrdinger equation with energy-dependent potential: has been noticed by quite a few authors. Jaulent and Miodek have used it to solve some nonlinear evolution equations with isospectral condition ξ_t=0. Li and Zhuang have further made use of (1) to expand the solvable class of nonlinear evolution equations. Several physical problems in absorption media can be reduced to the inverse scattoring problem of(1) (see [4]).