Site-Specific Detection of Free Radicals in Membranes Using an Amphiphilic Spin Trap

The detection of free radicals and related species has attracted considerable attention in recent years due to their critical roles in physiological and pathological processes. Among the various methods for the detection of free radicals, electron spin resonance coupled with spin-trapping technique has been an effective approach for the characterization and quantification of free radicals due to its high specificity. In this study, we designed and synthesized a novel amphiphilic spin trap, 2-(diethoxyphosphoryl)-2-heptadecanyl-3,4-dihydro-2H-pyrrole-1-oxide (DEPHdPO), from 5-(diethoxyphosphoryl)-5-methyl-1-pyrroline-N-oxide with a long hydrocarbon chain at the C-5 position of the pyrroline ring, providing the amphiphilic character. The free-radical-trapping ability of DEPHdPO was evaluated by capturing hydroxyl radicals (^·OH), superoxide anions (\( {\text{O}}_{2}^{ \cdot - } \)), and carbon-centered free radicals in a model membrane prepared from sodium dodecyl sulfate (SDS). The results indicate that the hydrophobic hydrocarbon chain of DEPHdPO can be inserted into the inner core of SDS micelles, and the hydrophilic nitronyl functional moiety is located on the surface layer. Thus, various free radicals, including ^·OH radicals, \( {\text{O}}_{2}^{ \cdot - } \) anions, and carbon-centered radicals could be site-specifically detected near the membrane surface. Moreover, DEPHdPO could be successfully located on the surface of thylakoid membranes, and the nearby photo-initiated \( {\text{O}}_{2}^{ \cdot - } \) anions could be trapped site-specifically.     

基于CAN总线的遥测数据处理模块软件设计

随着飞行器电子综合化技术的发展,数据总线在飞行器中得到大量应用。为满足某飞行器总线系统测量的需求,本文设计了一种基于CAN总线的遥测数据处理模块。硬件部分主要由CAN总线驱动器模块、DSP数字信号处理模块、FPGA逻辑处理模块组成。软件设计包括TMS320F28335的初始化,CAN总线数据处理和外部中断处理三部分。该模块用于某飞行器双路CAN总线数据的采集及处理,并经过了多次飞行试验验证。该模块简化了系统设计,实现了高速、可靠的CAN总线遥测数据处理。     

综合传动装置起动扭矩测试试验研究

低温环境起动性能是表征车辆动力性能的一项重要指标。对液力机械传动车辆而言,由于综合传动装置自身技术特点,改善车辆起动性能除应当考虑发动机自身起动阻力外,还应当考虑综合传动装置的起动阻力。在系统分析综合传动装置技术特点和功率流向的基础上,总结了发动机起动过程的主要特征,提出采用稳态试验与动态试验相结合的台架试验方法进行综合传动装置起动扭矩测试。以某高速履带车辆为研究对象,进行了综合传动装置起动扭矩测试。试验结果表明,传动油温的变化和各类油泵的功率消耗是决定综合传动装置起动扭矩大小的关键因素,为改进车辆总体设计和提高车辆起动性能提供了依据。     

Singer-Thorpe bases for special Einstein curvature tensors in dimension 4

Let (M, g) be a 4-dimensional Einstein Riemannian manifold. At each point p of M, the tangent space admits a so-called Singer-Thorpe basis (ST basis) with respect to the curvature tensor R at p. In this basis, up to standard symmetries and antisymmetries, just 5 components of the curvature tensor R are nonzero. For the space of constant curvature, the group O(4) acts as a transformation group between ST bases at T _p M and for the so-called 2-stein curvature tensors, the group Sp(1) ? SO(4) acts as a transformation group between ST bases. In the present work, the complete list of Lie subgroups of SO(4) which act as transformation groups between ST bases for certain classes of Einstein curvature tensors is presented. Special representations of groups SO(2), T ², Sp(1) or U(2) are obtained and the classes of curvature tensors whose transformation group into new ST bases is one of the mentioned groups are determined.     

Principal direction-based Hough transform for line detection

A robust and fast line detection method based on Hough transform (HT) is proposed in this paper. Edge pixels are extracted based on the summation and ratio of principal curvatures. Probabilistic sampling on the edge pixels is applied to reduce the count of voting. Then a one-to-one voting strategy is applied by taking advantages of the information of principal direction. The principal direction is also conducive for the successive accurate line segment extraction. The experiments demonstrate that the proposed method shows better locating accuracy and computation efficiency compared with several significant variations of HT.     

Synthesis of binuclear palladium complexes with a rigid phenylene bridge linker

The complexes [PdX₂Py]₂(di-NHC) (X = Br or Cl) in which di-NHC represents a di-N-heterocyclic carbene, featuring a rigid phenylene spacer between the carbene units, have been prepared from reactions of the corresponding diimidazolium halide salts with PdCl₂ in pyridine. The molecular structures of three of the complexes were determined by X-ray diffraction studies. The influences of different substitutions and of the halide ligand (Br or Cl) on the structure and reactivity of the complexes have been studied. The catalytic activity of the binuclear palladium complexes was tested in the Mizoroki–Heck reaction of styrene with bromobenzene.     

Influence of TiO2 impregnated with a novel copper(II) carboxylic porphyrin and its application in photocatalytic degradation of 4-Nitrophenol

A novel 5,15-di-[4-carboxylatomethoxy]phenyl-10,20-diphenylporphyrin, its copper complex and the corresponding metalloporphyrin-TiO₂ photocatalyst were synthesized and characterized by DRS, SEM, XRD, and FT–IR. The photocatalytic effects of anataseTiO₂ impregnated with this copper(II) porphyrin was investigated by photodegradation of 4-nitrophenol(4-NP) in aqueous solution under Xenon lamp irradiation. The results indicated that the photoactivity of copper(II) porphyrin-TiO₂ composite was evidently enhanced by the interaction between carboxyl of the porphyrin molecule and hydroxyls anchored on the TiO₂. Futhermore, the copper(II) carboxylic porphyrin displayed good adsorption behavior and activity of the dye-sensized TiO₂ system.     

Three-dimensional Octameric Assembly of Icosahedral M13 Units in [Au8Ag57(Dppp)4(C6H11S)32Cl2]Cl and its [Au8Ag55(Dppp)4(C6H11S)34][BPh4]2 Derivative

The high-dimensional (that is, three-dimensional (3D)) assembly of nanomaterials is an effective means of improving their properties; however, achieving this assembly at the atomic level remains challenging. Herein, we obtained a novel nanocluster, [Au₈Ag₅₇(Dppp)₄(C₆H₁₁S)₃₂C_l2]Cl (Dppp=1,3-bis(diphenylphosphino)propane) showing a 3D octameric assembly mode involving the kernel penetration of eight complete icosahedral Au@Ag₁₀Au₂ units for the first time. The atomically precise structure was determined by single-crystal X-ray diffraction, and further confirmed by thermogravimetric analysis, X-ray photoelectron spectroscopy, and electrospray ionization mass spectrometry measurements. Furthermore, ligand-induced transformation prompted the conversion of [Au₈Ag₅₇(Dppp)₄(C₆H₁₁S)₃₂Cl₂]Cl, with complete octameric fusion into [Au₈Ag₅₅(Dppp)₄(C₆H₁₁S)₃₄][BPh₄]₂, with incomplete octameric fusion. These observations will hopefully facilitate further research on the assembly of M₁₃ nanobuilding blocks.