Unoriented Laplacian maximizing graphs are degree maximal

A connected graph is said to be unoriented Laplacian maximizing if the spectral radius of its unoriented Laplacian matrix attains the maximum among all connected graphs with the same number of vertices and the same number of edges. A graph is said to be threshold (maximal) if its degree sequence is not majorized by the degree sequence of any other graph (and, in addition, the graph is connected). It is proved that an unoriented Laplacian maximizing graph is maximal and also that there are precisely two unoriented Laplacian maximizing graphs of a given order and with nullity 3. Our treatment depends on the following known characterization: a graph G is threshold (maximal) if and only if for every pair of vertices u,v of G, the sets N(u)?{v},N(v)?{u}, where N(u) denotes the neighbor set of u in G, are comparable with respect to the inclusion relation (and, in addition, the graph is connected). A conjecture about graphs that maximize the unoriented Laplacian matrix among all graphs with the same number of vertices and the same number of edges is also posed.     

Electrochemical properties of niosomes‐modified Au electrode and its interaction with 1‐anilino‐8‐naphthalene‐sulfonate

The gold electrode was modified by noisomes, prepared by sonicating the mixed solution of PEG 6000/Tween 80/Span 80/H₂O. Electrochemical cyclic voltammetry (CV) and impedance spectroscopy (EIS) were performed for characterizing the modification. The construction of multilayer films of octadecanethiol (ODT)‐niosomes had almost no pinholes, which elicited that niosomes‐coated electrode through ODT assembly was more effective immobilization compared to direct modification method. A large semicircle formation in the entire range of frequency indicated the complete electron‐transfer control for the redox reaction, implying a perfect blocking behavior. The Nyquist plot was consisting of two depressed semicircles after storage for 36 h in air, which implied a progressive and uniform construction manner, as expected for porous coatings. The modified electrode was used to investigate the interaction between 1‐anilino‐8‐naphthalene‐sulfonate (ANS) and noisomes. It was found that the low‐frequency semicircular arcs increase in diameter, indicating that the increase in the resistance R_p attributed mainly to the niosomes/solution interface. It was due to the binding of ANS to the niosomes‐modified electrode surface, exhibited against diffusing species through the pores. Copyright © 2009 John Wiley & Sons, Ltd.     

Lignanamides and Sesquiterpenoids from Stems of Mitrephora thorelii

The first phytochemical investigation on stems of Mitrephora thorelii led to the isolation of three new lignanamides, thoreliamides A–C ( 1 – 3 ), and a new sesquiterpenoid, thorelinin ( 4 ), together with ten known compounds. The structures of the new compounds were established on the basis of extensive spectroscopic analyses. Thoreliamide C is the first trimer derived from cinnamic acid amide units.     

酸度对CeCl3·nH2O晶体热分解过程的影响研究

采用热重-差式扫描量热法（TG—DSC）分析了不同酸度的盐酸-水合氯化铈饱和溶液中生成的CeCl3·nH2O晶体在空气氛围热分解脱水的过程，热分析表明酸度对CeCl3·nH2O晶体结晶形式有影响，氯化铈饱和溶液在盐酸中生成的CeCl3·nH2O晶体较商品CeCl3·nH2O晶体的热分解多一个恒温脱水失重的过程．X射线粉末衍射（XRD）结果表明此商品CeCl3·nH2O晶体为CeCl3·7H2O，盐酸-水合氯化铈饱和溶液中生成的CeCl3·nH2O晶体为含有不同个数结晶水的混合物．     

Effect of the ratio of transition dipole moments on few-cycle pulse propagation

Propagation of a few-cycle laser pulses in a dense V-type three-level atomic medium is investigated based on full-wave Maxwell-Bloch equations by taking the near dipole-dipole (NDD) interaction into account. We find that the ratio, γ, of the transition dipole moments has strong influence on the time evolution and split of the pulse: when γ≤ 1, the NDD interaction delays propagation and split of the pulse, and this phenomenon is more obvious when the value of γ is smaller; when γ = 2, the NDD interaction accelerates propagation and split of the pulse.     

The structural and optical properties of ZnO nanorod arrays

High quality vertical-aligned ZnO nanorod arrays were synthesized by a simple vapor transport process on Si (111) substrate at a low temperature of 520 °C. Field-emission scanning electron microscopy (FESEM) showed the nanorods have a uniform length of about 1 μm with diameters of 40-120 nm. X-ray diffraction (XRD) analysis confirmed that the nanorods are c-axis orientated. Selected area electron diffraction (SAED) analysis demonstrated the individual nanorod is single crystal. Photoluminescence (PL) measurements were adopted to analyze the optical properties of the nanorods both a strong UV emission and a weak deep-level emission were observed. The optical properties of the samples were also tested after annealing in oxygen atmosphere under different temperatures, deep-level related emission was found disappeared at 600 °C. The dependence of the optical properties on the annealing temperatures was also discussed.     

ZnSe单晶薄膜的MOCVD法生长

本文研究了常压MOCVD法制备宽禁带材料ZnSe的生长机制。通过经验公式和烟雾实验,从理论上和实验上分析了反应室的气流状态。观测了滞流层厚度及生长速率与位置、气流速度及衬底温度的关系。实现了反应器设计最优化,在热壁、常压、DEZ源的系统中也生长出高质量的ZnSe单晶外延层。     

Trace mild acid-catalysed Z → E isomerization of norbornene-fused stilbene derivatives: intelligent chiral molecular photoswitches with controllable self-recovery

Stilbene derivatives have long been known to undergo “acid-catalyzed” Z → E isomerization, where a strong mineral acid at high concentration is practically necessary. Such severe reaction conditions often cause undesired by-reactions and limit their potential application. Herein, we present a trace mild acid-catalyzed Z → E isomerization found with stilbene derivatives fused with a norbornene moiety. By-reactions, such as the migration of the C C double bond and electrophilic addition reactions, were completely inhibited because of the ring strain caused by the fused norbornene component. Direct photolysis of the E isomers at selected wavelengths led to the E → Z photoisomerization of these stilbene derivatives and thus constituted a unique class of molecular switches orthogonally controllable by light and acid. The catalytic amount of acid could be readily removed, and the Z → E isomerization could be controlled by turning on/off the irradiation of a photoacid, which allowed repeated isomerization in a non-invasive manner. Moreover, the Z isomer produced by photoisomerization could spontaneously self-recover to the E isomer in the presence of a catalytic amount of acid. The kinetics of Z → E isomerization were adjustable by manipulating catalytic factors and, therefore, unprecedented molecular photoswitches with adjustable self-recovery were realized.

Quantitative Z → E isomerization was catalyzed by trace mild acids to offer molecular switches orthogonally controllable by acid and light.