Comparing a mononuclear Zn(II) complex with hydrogen bond donors with a dinuclear Zn(II) complex for catalysing phosphate ester cleavage

Introducing ligand based hydrogen bond donors to increase the activity of a mononuclear Zn(II) complex for catalysing phosphate ester cleavage can be a more effective strategy than making the dinuclear analogue.     

A miniaturized HTS microwave receiver front-end subsystem for radar and communication applications

This paper presents a miniaturized high performance high temperature superconducting (HTS) microwave receiver front-end subsystem, which uses a mini stirling cryocooler to cool a high selective HTS filter and a low noise amplifier (LNA). The HTS filter was miniaturized by using specially designed compact resonators and fabricating with double-sided YBCO films on LAO substrate which has a relatively high permittivity. The LNA was specially designed to work at cryogenic temperature with noise figure of 0.27 dB at 71 K. The mini cryocooler, which is widely used in infrared detectors, has a smaller size (60 mm × 80 mm × 100 mm) and a lighter weight (340 g) than the stirling cryocoolers commonly used in other HTS filter subsystem. The whole front-end subsystem, including a HTS filter, a LNA, a cryocooler and the vacuum chamber, has a size of only φ120 mm × 175 mm and a weight of only 3.3 kg. The microwave devices inside the subsystem are working at 71.8 K with a consumed cooling power of 0.325 W. The center frequency of this subsystem is 925.2 MHz and the bandwidth is 2.7 MHz (which is a fractional bandwidth of 0.2%), with the gain of 19.75 dB at center frequency and the return loss better than ?18.11 dB in the pass band. The stop band rejection is more than 60 dB and the skirt slope is exceeding 120 dB MHz^?1. The noise figure of this subsystem is less than 0.8 dB. This front-end subsystem can be used in radars and communication systems conveniently due to it’s compact size and light weight.     

Relative Transpose and its Dual with Respect to a Bimodule

For a class of modules \(\mathcal {X}\), we introduce the \(\mathcal {X}\)-transpose of a module with respect to a bimodule, which unifies some well-known transposes. Let \(\mathcal {V}\) be a subclass of \(\mathcal {X}\). The relations between \(\mathcal {X}\)-transposes and \(\mathcal {V}\)-transposes are investigated under the condition that \(\mathcal {V}\) is a generator or cogenerator of \(\mathcal {X}\). The dual aspects of \(\mathcal {X}\)-transposes are also discussed. Then we give some applications of these results. In particular, the dual counterparts of Gorenstein transposes are established.     

求一阶数值微分的L-广义解方法cTSVD

<正>1引言数值微分也就是给定一个函数在一个区间或某些离散点上的扰动数据来求函数的导数,它产生于很多实际问题当中,比如,图象处理中的边界识别问题;Abel积分方程的求解问题;化学中波谱的波峰识别问题.以及一些数学物理反问题当中.数值微     

Effect of Fe on the glass-forming ability,structure and devitrification behavior of Zr–Cu–Al bulk glass-forming alloys

We report on the glass-forming ability and devitrification behavior of Zr₆₀Cu₃₀Al₁₀, Zr₆₀Cu₂₅Al₁₀Fe₅ and Zr_62.5Cu_22.5Al₁₀Fe₅ bulk glass-forming alloys on heating. The effect of Fe addition on the structure of Zr–Al–Cu alloys is also discussed. Crystallization kinetics and structural changes in the glassy alloys were studied using X-ray diffraction, transmission electron microscopy, differential scanning and isothermal calorimetry methods. The results indicate that good glass-formers, such as Zr_62.5Cu_22.5Al₁₀Fe₅, are located somewhat beyond the equilibrium eutectic point. Possible phase separation in the supercooled liquid on heating and electron beam-induced in situ crystallization are observed and discussed.     

Skin Thickness and β-Crystals Development in Injection-Molded iPP Along the Flow Direction

In this study, iPP was injection molded at 180°C, 200°C, and 220°C. According to polarization optical microscopy (POM) results, for a given part, the skin thickness steadily decreases along the flow direction. However, at the same distance from the gate, the skin thickness of the parts molded at lower melt temperature is larger than that molded at higher melt temperature. It is found that flow time (here, the time taken for melt to pass the specific position along the flow direction) and melt temperature are two significant factors leading to this phenomenon, while the gate size is another one.

The DSC and WAXD results show that the relative fraction of β-form crystals, for a specific part, decreases along the flow direction, which is mainly determined by flow time. However, for the parts molded at different molding temperatures, the fraction of the β-form crystals is mainly determined by the molding temperature, though this influence is very complex.     

Effect of Stretching on β-Phase Content of Isotactic Polypropylene Melt Containing β-Nucleating Agent

Pure isotactic polypropylene (iPP) and that containing 0.2 wt% of a β-nucleating agent (β-NA) were extruded through a slit die. Simultaneously, the extruded melt was stretched at the die exit with different stretching rates (SR). The change of β-phase content with different SR was investigated by differential scanning calorimetry (DSC) and wide-angle X-ray diffraction (WAXD). The results indicate that, for pure iPP, the content of β-phase first increases with increasing SR till it reaches a maximum and then it gradually decreases. However, for the case of β-nucleated iPP, it decreases monotonously with increasing SR. The spatial confinement is considered as the best explanation for the suppression of β-phase in the nucleated iPP melt upon stretching.     

Chemoselective Borane‐Catalyzed Hydroarylation of 1,3‐Dienes with Phenols

A B(C₆F₅)₃‐catalyzed hydroarylation of a series of 1,3‐dienes with various phenols has been established through a combination of theoretical and experimental investigations, affording structurally diverse ortho‐allyl phenols. DFT calculations show that the reaction proceeds through a borane‐promoted protonation/Friedel–Crafts pathway involving a π‐complex of a carbocation–anion contact ion pair. This protocol features simple and mild reaction conditions, broad functional‐group tolerance, and low catalyst loading. The obtained ortho‐allyl phenols could be further converted into flavan derivatives using B(C₆F₅)₃ with good cis diastereoselectivity. Furthermore, this transformation was applied in the late‐stage modification of pharmaceutical compounds.     

Platinum/Nickel Bicarbonate Heterostructures towards Accelerated Hydrogen Evolution under Alkaline Conditions

Heterostructured nanomaterials, generally have physicochemical properties that differ from those of the individual components, and thus have potential in a wide range of applications. New platinum (Pt)/nickel bicarbonate (Ni(HCO₃)₂) heterostructures are designed for an efficient alkaline hydrogen evolution reaction (HER). Notably, the specific and mass activity of Pt in Pt/Ni(HCO₃)₂ are substantially improved compared to the bare Pt nanoparticles (NPs). The Ni(HCO₃)₂ provides abundant water adsorption/dissociation sites and modulate the electronic structure of Pt, which determine the elementary reaction kinetics of alkaline HER. The Ni(HCO₃)₂ nanoplates offer a platform for the uniform dispersion of Pt NPs, ensuring the maximum exposure of active sites. The results demonstrate that, Ni(HCO₃)₂ is an effective catalyst promoter for alkaline HER.     

Stereoconvergent,Redox‐Neutral Access to Tetrahydroquinoxalines through Relay Epoxide Opening/Amination of Alcohols

We present an economical catalytic procedure to convert readily available 1,2‐diaminobenzenes and terminal epoxides into valuable 1,2,3,4‐tetrahydroquinoxalines in a highly enantioselective fashion. This procedure operates through relay zinc and iridium catalysis, and achieves redox‐neutral and stereoconvergent production of valuable chiral heterocycles from racemic starting materials with water as the only side product. The use of commercially available reagents and catalysts and a convenient procedure also make this catalytic method attractive for practical application.