Synthesis，Crystal Structure and Thermode－composition Kinetics of Copper（Ⅱ） Complex with bis－（Schiffbase） Derived from 3－Methoxysalicylaldehyde and Ethanolamine

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Liquid chromatography tandem mass spectrometry method for determination of bisoprolol in human plasma using d5‐bisoprolol as the internal standard

A simple, reliable and sensitive liquid chromatography tandem mass spectrometry (LC‐MS/MS) protocol was developed and validated for quantification of bisoprolol in human plasma. The sample was pretreated with a simple procedure of protein precipitation and an isotope‐labeled d5‐bisoprolol was used as internal standard. The chromatographic separation was performed on a Capcell Pak C₁₈ MG III column (100 mm × 2.0 mm, 5 µm). The protonated ion of the analyte was detected in positive ionization by multiple reaction monitoring mode. The mass transition pairs of m/z 326.3 → 116.3 and m/z 331.3 → 121.3 were used to detect bisoprolol and the internal standard, respectively. Linearity, accuracy, precision, recovery, matrix effect, dilution test and stability were evaluated during method validation over the range of 0.5–100 ng/mL. The validated method was successfully applied to analyze human plasma samples in a bisoprolol bioavailability study. Copyright © 2009 John Wiley & Sons, Ltd.     

Topographies of Organized Monolayer of α-Amylase Observed by Atomic Force Microscopy

Preparing the organized ultrathin film of proteins is the key to developing of protein-based molecular devices such as biosensors. In the past, the organized molecular layers were fabricated by the means of Langmuir-Blodgett (LB), which utilized the amphipathy of molecules. Molecular deposition (MD) which is based on the electrostatic interaction between the charged substrates and oppositely charged absorbate is a new and versatile method for preparing organized self-assembled ultrathin film…     

Microwave-Promoted Rapid Synthesis of 1-Aryl-1,2,3-Triazoles

1, 2, 4- and 1, 2, 3-triazole derivatives have found wide applications as plant growth regulators1, bactericides and medical fungicides2, insecticides3 and in dyeing and color development4.One of the general routes of synthesis of 1-aryl-1, 2, 3-triazoles was to treat aryl azides with a-keto phosphorus ylides in dry refluxing benzene for 0.5 to 2 days5. Herein we report, for the first time, a very quick and simple, microwave-promoted synthesis of 1-aryl-1, 2, 3-triazoles 3 from aryl azides 1 an…     

From Lead Iodide to a Radical Form Lead‐Iodide Superlattice: High Conductance Gain and Broader Band for Photoconductive Response

Superlattice materials offer new opportunities to modify optical and electrical properties of recently emerging 2D materials. The insertion of tetraethylbenzidine (EtDAB) into interlamination of the established 2D PbI₂ semiconductor through a mild solution method yielded the first lead iodide superlattice, EtDAB?4PbI₂ (EtDAB=tetraethylbenzidine), with radical and non‐radical forms. The non‐radical form has a non‐ionic structure that differs from the common ionic structures for inorganic–organic hybrid lead halides. The radical form shows five orders of magnitude greater conductance and broader photoconductive response range (UV/Vis → UV/Vis‐IR), than pure PbI₂ and the non‐radical form of the superlattice.     

Facet-Control versus Co-Catalyst-Control in Photocatalytic H2 Evolution from Anatase TiO2 Nanocrystals

Titanium dioxide (TiO₂) and, in particular, its anatase polymorph, is widely studied for photocatalytic H₂ production. In the present work, we examine the importance of reactive facets of anatase crystallites on the photocatalytic H₂ evolution from aqueous methanol solutions. For this, we synthesized anatase TiO₂ nanocrystals with a large amount of either {001} facets, that is, nanosheets, or {101} facets, that is, octahedral nanocubes, and examined their photocatalytic H₂ evolution and then repeated this procedure with samples where Pt co-catalyst is present on all facets. Octahedral nanocubes with abundant {101} facets produce >4 times more H₂ than nanosheets enriched in {001} facets if the reaction is carried out under co-catalyst-free conditions. For samples that carry Pt co-catalyst on both {001} and {101} facets, faceting loses entirely its significance. This demonstrates that the beneficial role of faceting, namely the introduction of {101} facets that act as electron transfer mediator is relevant only for co-catalyst-free TiO₂ surfaces.     

极大谱距离的注记

Two equivalent conditions are given for the non-commutative unital C^＊-subalgebras of B（H） algebras A and B to be quantum C^＊ independent.     

The qualitative analysis of a class of planar Filippov systems

We use the theory of differential inclusions, Filippov transformations and some appropriate Poincaré maps to discuss the special case of two-dimensional discontinuous piecewise linear differential systems with two zones. This analysis applies to uniqueness and non-uniqueness for the initial value problem, stability of stationary points, sliding motion solutions, number of closed trajectories, existence of heteroclinic trajectories connecting two saddle points forming a heteroclinic cycle and existence of the homoclinic trajectory     

Characterization of signs change of nonlinear refraction in ZnSe based on a modified double 4f imaging system with a phase object

Signs change of nonlinear refractive index in ZnSe is observed by employing a modified double 4f imaging system at the wavelength of 800 nm using picosecond pulses with different pulse energies. This process results from the competition of the bound electronic nonlinear refraction and the free carrier refraction. At low intensity, positive nonlinear refraction is obtained, which is attributed to bound electrons. As the increase of laser beam intensity, the nonlinear refractive index become small, and changes to negative. This is ascribed to free carriers generated by two-photon absorption. Additionally, the nonlinear refractive index of bound electron and the refractive index change of free carrier are determined unambiguously by a simple method.     

有机过氧化物-芳叔胺体系引发甲基丙烯酸甲酯聚合的研究

以过氧化二酰(BPO、LPO)或有机过氧化氢物(TBH、CHP)和芳叔胺如DMA或对位具有不同取代基的衍生物组成的引发体系进行MMA聚合,研究过氧化物与胺的结构对聚合的影响。结果表明,过氧化二酰的活性要比有机过氧化氢物大,其顺序为BPO>LPO>CHP>TBH。对于BPO-芳叔胺或LPO-芳叔胺体系,芳叔胺中给电子取代基能提高聚合速度,而吸电子取代基能降低聚合速度。测定了MMA聚合的总活化能E_α,BPO-芳叔胺体系时E_α=36-54kJ/mole,LPO-芳叔胺体系时E_α=56-71kJ/mole;还研究聚合动力学。