K3ReH6 – Synthese,Struktur und magnetische Eigenschaften

K₃ReH₆ – Synthesis, Structure, and Magnetic Properties K₃ReH₆ and K₃ReD₆ were synthesized by the reaction of potassium hydride (deuteride) with rhenium powder under a hydrogen pressure between 3000–3500 bar at 850 K. X-ray investigations on powdered samples and elastic neutron diffraction experiments on the deuterated compound at the triple axis spectrometer TAS 1 in the temperature range 5–600 K led to the atomic arrangement, which corresponds to that of the cryolite with [ReH₆]^3–-octahedra as characteristic units. Magnetic susceptibility measurements in the temperature range from 3.5 K and room temperature revealed a weak temperature independent paramagnetism. Quantum mechanical calculations confirm these facts and show in detail that the large value of the spin-orbit coupling parameter is essential for the magnetic behaviour.     

Electromyography Activity of Vastus Medialis Obliquus and Vastus Lateralis Muscles During Lower Limb Proprioceptive Neuromuscular Facilitation Patterns in Individuals with and without Patellofemoral Pain Syndrome

Objective: Exercise therapy to strengthen quadriceps muscle is recommended in rehabilitation program for people with patellofemoral pain syndrome (PFPS). This study aimed to investigate the electromyography (EMG) activity of vastus medialis obliquus (VMO), vastus lateralis (VL) and VMO/VL ratio during PNF in individuals with and without PFPS. Methods: 26 persons with PFPS and 26 healthy subjects participated to study. All subjects performed PNF patterns (Flexion-Adduction-External Rotation (D₁FL), Extension-Adduction-External Rotation (D₂EX), D₁FL+ load, D₂EX+ load) and straight leg raise (SLR). The normalized EMG activity of VMO, VL and VMO/VL ratio were measured and analyzed using repeated measure ANOVA. Results: There were significant main effects of group and exercises for the both VMO and VL (p<0.05). It was found that except SLR and D₂EX, in the other motions PFPS group had lower VMO activity compared to healthy group (p<0.05). For VL except SLR, in the other motions PFPS group had lower VL activity too (p<0.05). The PNF patterns activated VMO more than SLR, however it was not significant (p>0.05). Also; there weren''t any significant difference between the two groups in VMO/VL activation ratios. Also, performing the PNF patterns with load increased VMO and VL muscles activity significantly (p<0.05). It also found that in PFPS group the VMO/VL ratio values in PNF patterns were significantly more than SLR and the highest VMO/VL ratio value (0.96) was found during D₂EX. Conclusion: The PNF patterns due to provide optimal VMO/VL ratio value than SLR and proper balance between these two muscles can be recommended in rehabilitation of individuals with PFPS.     

无损残余应力测量及其新技术

简述及比较了主要的残余应力无损测量技术，重点为磁力法，并介绍一台新的磁力仪MAPS，且对MAPS及传统磁力仪作了比较，同时以X射线及中子衍射得到的结果验证了MAPS的可靠性，也介绍了文献上较少见的火车钢轨残余应力分布图。     

透明质酸纳米材料在荧光/光声成像和光疗中的应用

荧光/光声成像和光疗技术的生物医学应用引起了人们越来越多的关注, 然而很多荧光/光声造影剂存在生物相容性较差, 缺乏肿瘤靶向性, 信噪比较低, 功能单一等共性问题, 严重限制其诊疗应用. 透明质酸具有优异的生物相容性和主动肿瘤靶向性, 可被透明质酸酶降解, 并且易于化学修饰和实现多种超分子弱相互作用力协同工作. 因此, 人们将透明质酸与荧光/光声造影剂结合制备纳米材料, 使其在细胞乃至活体的标记性能和治疗效果获得了很大的改善. 本文综述了将两类物质结合制备纳米材料的方法, 着重阐述了纳米材料的结构与性能关系, 为其未来设计和开发提供了指导, 最后对存在的主要问题以及未来的重要研究方向进行了分析和展望.     

Structural and optical investigation of nonpolar α-plane GaN grown by metalben organic chemical vapour deposition on r-plane sapphire by neutron irradiation

Nonpolar (1120) α-plane GaN films are grown by metal-organic chemical vapour deposition (MOCVD) on r-plane (1102) sapphire. The samples are irradiated with neutrons under a dose of 1 × 10¹⁵ cm^-2. The surface morphology, the crystal defects and the optical properties of the samples before and after irradiation are analysed using atomic force microscopy (AFM), high resolution X-ray diffraction (HRXRD) and photoluminescence (PL). The AFM result shows deteriorated sample surface after the irradiation. Careful fitting of the XRD rocking curve is carried out to obtain the Lorentzian weight fraction. Broadening due to Lorentzian type is more obvious in the as-grown sample compared with that of the irradiated sample, indicating that more point defects appear in the irradiated sample. The variations of line width and intensity of the PL band edge emission peak are consistent with the XRD results. The activation energy decreases from 82.5 meV to 29.9 meV after irradiation by neutron.     

Acceleration Effect in the Field of Neutron Star with Electric and Magnetic Charge and Magnetic Moment

The expression of acceleration in the external gravitational field of neutron star with electric and magnetic charge and magnetic moment is obtained. And some gravitational effects and properties of the field are discussed respectively from the contributions of the electric and magnetic charge and magnetic moment on the acceleration.     

Adducts of (C6F5)3B with Selected Nitrogen

The Lewis acid (C₆F₅)₃B was reacted with ICN, NH₂CN, C₃N₃X₃ (X = H, Cl, F). The resulting Lewis acid base adducts ( 1—5 ) were fully characterized by analytic and spectroscopic methods. Additionally, the structures of the adducts 1—4 were determined by single crystal X‐ray analyses. It has been qualitatively shown, that a high field shift of the ¹¹B as well as the ¹⁹F NMR resonances of the o‐F atoms of the C₆F₅‐substituents suggests a longer B—N distance.     

Aufbau und Abbau von (NH4)[BF4] und H3N‐BF3

Production and Decomposition of (NH₄)[BF₄] and H₃N‐BF₃ (NH₄)[BF₄] is produced as single crystals during the reaction of elemental boron and NH₄HF₂ (B : NH₄HF₂ = 1 : 2) and NH₄F (B : NH₄F = 1 : 4), respectively, in sealed copper ampoules at 300 °C. The crystal structure (baryte type, orthorhombic, Pnma, Z = 4) was redetermined at ambient temperature (a = 909.73(18), b = 569.77(10), c = 729.47(11) pm, R_all = 0.0361) and at 140 K (a = 887.3(2), b = 574.59(12), c = 717.10(12) pm, R_all = 0.0321). Isolated (NH₄)⁺ and [BF₄]^— tetrahedra are the important building units. The thermal behaviour of (NH₄)[BF₄] was investigated under inert (Ar, N₂) and reactive conditions (NH₃) with the aid of DTA/TG and DSC measurements and with in‐situ X‐ray powder diffraction as well. Finally, (NH₄)[BF₄] is decomposed yielding NH₃ and BF₃, BN is not produced under the current conditions. Colourless single crystals of H₃N‐BF₃ were prepared directly from the components NH₃ and BF₃. The crystal structure was determined anew at 293 and 170 K (orthorhombic, Pbca, Z = 8, a = 815.12(10), b = 805.91(14), c = 929.03(12) pm, R_all = 0.0367; a = 807.26(13), b = 800.48(10), c = 924.31(11) pm, R_all = 0.0292, T = 170 K). The crystal structure contains isolated molecules H₃N‐BF₃ in staggered conformation with a B‐N distance of 158 pm. The thermal behaviour of H₃N‐BF₃ was studied likewise.     

Structure and dynamics of solutions of a polystyrene–polybutadiene pentablock copolymer in a styrene‐selective solvent

We have examined solutions of a polystyrene–polybutadiene pentablock copolymer in 1,4‐dioxane, a slightly selective solvent for polystyrene and a θ solvent for polybutadiene, with static light scattering (SLS), dynamic light scattering (DLS), and small‐angle neutron scattering (SANS). The SANS data have been analyzed with the Percus–Yevick model to represent the scattering from interacting cores, approximated as hard spheres, and with a Lorentzian function to represent the scattering from unassociated and associated polymer chains. The SANS data at 25 °C clearly reveal interacting domains, approximately 6 nm in radius, formed by the association of the insoluble polybutadiene block in the 20% sample. The 4% sample does not show such domains, whereas the 7% sample represents an intermediate situation, with both unassociated polymer and associated polymer. At higher temperatures, the domains dissolve. The DLS data for samples with concentrations of 2–22% show two diffusive modes: a fast mode corresponding to the cooperative dynamics of concentration fluctuations and a slow mode corresponding to the diffusion of clusters. The large length‐scale heterogeneities, indicated by the strong angular dependence of SLS, implies that the small microdomains of about 10–15 polybutadiene blocks are bridged by the polystyrene chains, forming large aggregates with randomly distributed crosslinks on length scales much larger than the domain size. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 2807–2816, 2002     

CsC2H: Synthese,Kristallstruktur und spektroskopische Eigenschaften

CsC₂H: Synthesis, Crystal Structure, and Spectroscopic Properties CsC₂H was synthesised by the reaction of caesium solved in liquid ammonia with acetylene. The crystal structure could be solved and refined from X‐ray and neutron powder diffraction data (space group: R3c, Z = 18). The structure is characterised by C₂H^– trimers which are surrounded by caesium ions. Spectroscopic investigations (IR and Raman) of the stable monoalkalimetal acetylides mainly confirm the data given in the literature and show that the alkalimetal cation has a marked influence on the vibrational properties of the C₂H^– anion.