A novel stereoselective synthesis of 1,2-trans-thioaldoses

A mild and one-pot protocol for the efficient and stereoselective synthesis of 1,2-trans-aldosyl mercaptans is presented.     

Benzofuran–isatin Hybrids: Design,Synthesis, and In Vitro Anti‐cancer Activities

A series of novel benzofuran–isatin hybrids 6a – s tethered through propylene and butylene were designed, synthesized, and evaluated for their in vitro anti‐cancer activities against HepG2 (liver carcinoma), Hela (cervical cancer), A549 (lung adenocarcinoma), DU145 (prostatic cancer), SKOV3 (ovarian carcinoma), MCF‐7 (breast cancer), and drug‐resistant MCF‐7/DOX (doxorubicin‐resistant MCF‐7) human cancer cell lines. The majority of the synthesized hybrids displayed weak to moderate in vitro activities against the tested seven cancer cell lines, but the enriched structure–activity relationship may pave the way for further optimization.     

Benign Recycling of Spent Batteries towards All-Solid-State Lithium Batteries

Lithium-ion batteries (LIBs) are one of the most significant energy storage devices applied in power supply facilities. However, a huge number of spent LIBs would bring harmful resource waste and environmental hazards. In this study, a benign hydrometallurgical method using phytic acid as precipitant is proposed to recover useful metallic Mn ions from spent LiMn₂O₄ batteries. Besides Mn-based cathodes, this recovery process is also applicable for other commercial batteries. More importantly, for the first time, the as-obtained manganous complex is employed as a nanofiller in a polyethylene oxide matrix to largely improve Li⁺ conductivity and transference number. As a result, when applied in all-solid-state lithium batteries, high capacity and outstanding cyclic stability are achieved with capacity retention of 86.4 % after 60 cycles at 0.1 C. The recovery of spent lithium batteries not only has benefits for the environment and resources, but also shows great potential application in all-solid-state lithium batteries, which opens up a costless and efficient circulation pathway for clean and reliable energy storage systems.     

Studies of Adsorption Kinetics and Defects of Self‐Assembled Thiol Monolayers on Gold by Capacitance Plane Plot

The capacitive property of an electrode/electrolyte interface can be described by complex capacitance. The capacitance plane plots (CPPs) of ideal polarized and kinetic controlled electrodes are derived based on the concept of complex capacitance. By using CPPs, the capacitance of electrode/electrolyte interface can be conveniently determined. In this work, CPPs obtained in ac impedance experiments are employed for the first time in studying the kinetics of adsorption process of the thiol monolayer. The coverage of octadecanethiol (ODT) monolayer on gold is examined as a function of adsorption time. The adsorption process of ODT molecules on gold exhibits two distinct phases: an initial rapid step followed by a slow one. The simple Langmuir model best explains our experimental data in the initial adsorption stage. CPPs and cyclic voltammetry (CV) indicate that, in the initial adsorption step, the ODT monolayer contains defects whose number decreases with the increasing of adsorption time.     

基于蒙特卡洛方法的钛氧化物忆阻器辐射损伤研究

纳米钛氧化物忆阻器有望成为新一代阻性存储器基本单元并应用于辐射环境中的航天器控制及数据存储系统. 辐射能量, 强度, 方向, 持续时间等要素发生改变均可能对钛氧化物忆阻器受到的辐射损伤构成影响, 然而, 目前尚无相关具体研究. 基于以蒙特卡洛方法为核心的SRIM仿真, 本文针对宇宙射线主体组成部分——质子及 α射线定量研究了各个辐射要素与钛氧化物忆阻器辐射损伤的关联, 依据器件实测数据研究了辐射要素与导通阻抗, 截止阻抗及氧空缺迁移率等忆阻器主要参数的关系, 进一步利用SPICE仿真讨论了辐射对杂质漂移与隧道势垒共存特性的影响, 从而为评估及降低钛氧化物忆阻器辐射损伤, 提高器件应用于辐射环境的可靠性提供依据.     

Effective condition numbers and small sample statistical condition estimation for the generalized Sylvester equation

In this paper,we investigate the effective condition numbers for the generalized Sylvester equation(AX-YB,DX-YE)=(C,F),where A,D∈R m×m,B,E∈R n×n and C,F ∈ R m×n.We apply the small sample statistical method for the fast condition estimation of the generalized Sylvester equation,which requires O(m2n+mn2) flops,comparing with O(m3+n3) flops for the generalized Schur and generalized HessenbergSchur methods for solving the generalized Sylvester equation.Numerical examples illustrate the sharpness of our perturbation bounds.     

Electron transfer between ferrocene-modified Au/octadecanethiol/lipid BLM electrode and redox couples in solution

Bilayers incorporated with ferrocene consisting of self-assembled octadecanethiol and lipid monolayer on gold substrates were fabricated. Its electrochemical behaviors in solutions containing different redox couples were investigated by cyclic voltammetry and ac impedance. The transmembrane electron transfer reaction across octadecanethiol self-assembled film and an adsorbed phospholipid layer mediated by ferrocene have been observed in the solution of Fe(CN)6(3-/4-). The formal potential difference between mediator in bilayer lipid membrane (BLM) and redox couple in solution has a great impact on the transmembrane electron transfer behavior. The ferrocene-modified BLM electrodes might be useful for constructing a bilayer-based electrochemical current rectifying device.     

Interplay of mechanical and binding properties of Fibronectin type I

Fibronectins (FNs) are a major component of the extracellular matrix (ECM), and provide important binding sites for a variety of ligands outside and on the surface of the cell. Similar to other ECM proteins, FNs are consistently subject to mechanical stress in the ECM. Therefore, it is important to study their structure and binding properties under mechanical stress and understand how their binding and mechanical properties might affect each other. Although certain FN modules have been extensively investigated, no simulation studies have been reported for the FN type I (Fn1) domains, despite their prominent role in binding of various protein modules to FN polymers in the ECM. Using equilibrium and steered molecular dynamics simulations, we have studied mechanical properties of Fn1 modules in the presence or the absence of a specific FN-binding peptide (FnBP). We have also investigated how the binding of the FnBP peptide to Fn1 might be affected by tensile force. Despite the presence of disulfide bonds within individual Fn1 modules that are presumed to prevent their extension, it is found that significant internal structural changes within individual modules are induced by the forces applied in our simulations. These internal structural changes result in significant variations in the accessibility of different residues of the Fn1 modules, which affect their exposure, and, thus, the binding properties of the Fn1 modules. Binding of the FnBP appears to reduce the flexibility of the linker region connecting individual Fn1 modules (exhibited in the form of reduced fluctuation and motion of the linker region), both with regard to bending and stretching motions, and hence stabilizes the inter-domain configuration under force. Under large tensile forces, the FnBP peptide unbinds from Fn1. The results suggest that Fn1 modules in FN polymers do contribute to the overall extension caused by force-induced stretching of the polymer in the ECM, and that binding properties of Fn1 modules can be affected by mechanically induced internal protein conformational changes in spite of the presence of disulfide bonds which were presumed to completely abolish the capacity of Fn1 modules to undergo extension in response to external forces.     

Vortex states in soft magnets in two and three dimensions

The magnetization curves of arrays of near-spherical soft ferromagnetic particles are compared with those of quasi-two-dimensional dots with similar radius prepared by a rapid e-beam lithographic technique. Curves for the three-dimensional particles are anhysteretic and fit a M(H)/M_s=tanh(cμ₀H) law, whereas the two-dimensional arrays show irreversible segments in the first and third quadrants where the planar vortex state transforms to a collinear state by discontinuous rotation of magnetization about an axis perpendicular to the vortex axis. The additional symmetry of the spherical particle allows this rotation to occur continuously, without energy barriers due to the demagnetizing field.