新型2-胺基-1,3,4-噻二唑类化合物的合成及其抗肿瘤活性的研究

设计合成了一系列新型的N1-(5-取代基-1,3,4-噻二唑-2-基)-N3-取代苯基-脲类化合物,并测定了它们的抗肿瘤活性.标题化合物对肿瘤转移的生物活性实验是以荷Lewis肺癌小鼠为模型的.生物活性表明部分标题化合物对肿瘤的转移和肿瘤生长具有较好的抑制作用.其结构经元素分析、红外光谱及1H NMR确证.     

含脱氢松香骨架的1,8-萘酰亚胺衍生物的合成及其对阴离子的识别

以歧化松香胺为原料合成了6个新型含脱氢松香骨架的1,8-萘酰亚胺衍生物2a～2b和3a～3d,其结构用1H NMR,13C NMR,MS和元素分析进行了表征.对3a～3d进行了阴离子识别研究,并对其识别机理进行了讨论.     

常压高频放电等离子体炬改进制备CO2/CH4重整用Ni/MgO催化剂

比较了常规法、等离子体炬法和等离子体炬辅助焙烧法制得的Ni/MgO催化剂上CO2/CH4重整反应性能差异,并利用X射线衍射、透射电镜、X射线光电子能谱和CO2程序升温表面反应等技术对反应前后催化剂进行了表征,结果表明,采用等离子体炬辅助焙烧法制备的催化剂上Ni晶粒粒径小,分散度较高,低温活性和抗积炭性能较高;在常压,7...     

A hevein-like protein and a class I chitinase with antifungal activity from leaves of the paper mulberry

Paper mulberry (Broussonetia papyrifera, syn. Morus papyrifera L.) is a Chinese traditional medicine and its low‐molecular‐weight extracts are reported to have antifungal activity. In this study, two proteins (PMAPI and PMAPII) with activity against Trichoderma viride were obtained from paper mulberry leaves with a fast protein liquid chromatography (FPLC) unit. The purification protocol employed (NH₄)₂SO₄ precipitation, ion‐exchange chromatography and hydrophobic‐interaction chromatography on FPLC. Molecular masses were 18,798 Da for PMAPI, and 31,178 Da for PMAPII determined by Matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry. Peptide mapping fingerprint analysis showed that PMAPI has no peptides similar to PMAPII. N‐terminal amino acid sequencing revealed that PMAPI is a hevein‐like protein, and PMAPII is a class I chitinase. They both had a half‐maximal inhibitory concentration (IC50) of 0.1 µg/µL against T. viride. This is the first report of high‐molecular‐weight extracts with antifungal activity from paper mulberry. Copyright © 2011 John Wiley & Sons, Ltd.     

Spatial bandgap engineering along single alloy nanowires

Bandgap engineering of semiconductor nanowires is important in designing nanoscale multifunctional optoelectronic devices. Here, we report a facile thermal evaporation method, and realize the spatial bandgap engineering in single CdS(1-x)Se(x) alloy nanowires. Along the length of these achieved nanowires, the composition can be continuously tuned from x = 0 (CdS) at one end to x = 1 (CdSe) at the other end, resulting in the corresponding bandgap (light emission wavelength) being modulated gradually from 2.44 eV (507 nm, green light) to 1.74 eV (710 nm, red light). In spite of the existing composition (crystal lattice) transition along the length, these multicolor nanowires still possess high-quality crystallization. These bandgap engineered nanowires will have promising applications in such as multicolor display and lighting, high-efficiency solar cells, ultrabroadly spectral detectors, and biotechnology.     

Communication: vacuum ultraviolet laser photodissociation studies of small molecules by the vacuum ultraviolet laser photoionization time-sliced velocity-mapped ion imaging method

We demonstrate that the vacuum ultraviolet (VUV) photodissociation dynamics of N(2) and CO(2) can be studied using VUV photoionization with time-sliced velocity-mapped ion imaging (VUV-PI-VMI) detection. The VUV laser light is produced by resonant sum frequency mixing in Kr. N(2) is used to show that when the photon energy of the VUV laser is above the ionization energy of an allowed transition of one of the product atoms it can be detected and characterized as the wavelength is varied. In this case a β parameter = 0.57 for the N((2)D°) was measured after exciting N(2)(o(1)Π(u), v(') = 2, J(') = 2) ← N(2)(X(1)Σ(g) (+), v(") = 0, J(") = 1). Studies with CO(2) show that when there is no allowed transition, an autoionization resonance can be used for the detection of a product atom. In this case it is shown for the first time that the O((1)D) atom is produced with CO((1)Σ(+)) at 92.21 nm. These results indicate that the VUV laser photodissociation combined with the VUV-PI-VMI detection is a viable method for studying the one-photon photodissociation from the ground state of simple molecules in the extreme ultraviolet and VUV spectral regions.     

Ti0.10Zr0.15V0.35Cr0.10Ni0.30+5wt% LaNi5复合储氢合金的电化学性能与协同效应

为了改善钛钒基固溶体合金的电化学性能,利用两步电弧熔炼法制备复合储氢合金Ti0.10Zr0.15V0.35Cr0.10Ni0.30+5wt%LaNi5,X-射线衍射(XRD)和场发射扫描电镜-能谱(FESEM-EDS)显示:复合储氢合金的主相是体心立方结构的钒基固溶体相和六方结构的C14 Laves相,复合过程中生成了第二相。电化学测试结果表明:复合合金电极的P-C-T特征、活化性能、最大放电容量、循环稳定性、低温放电性能和动力学特性均较母体合金有显著改善。复合合金电极的活化周期数为5,最大放电容量为353.9 mAh.g-1,233 K时低温放电能力为50.26%。该复合合金电极的最大储氢容量、平台压、电荷转移电阻和交换电流密度均存在协同效应;在任意循环、在高/低温下以及在高倍率放电过程中,该复合合金电极的放电容量均存在协同效应。     

Microwave-assisted synthesis of α-hydroxy aromatic ketones from α-bromo aromatic ketones in water

A reaction ofα-bromo aromatic ketones in water with microwave irradiation gave the correspondingα-hydroxy aromatic ketones in good yields.The use of microwaves was found to significantly improve yields and shorten the reaction time.This reaction afforded a very clean,convenient method for the synthesis ofα-hydroxy aromatic ketones.     

High performance liquid chromatography with immobilized Ru(bpy)_3~(2+)-KMnO_4 chemiluminescence detection and its application in metabolism of repaglinide in pig liver microsomes

A novel high performance liquid chromatography-chemiluminescence（HPLC-CL） method for investigation of in vitro metabolism of repaglinide in pig liver microsomes with microdialysis sampling technique was developed.The chromatographic separation was performed on a Hypersil BDS-C18 column with an isocratic mobile phase consisting of methanol and 0.01 mol/L KH₂PO₄（pH 3.0）（volume ratio 75:25） at a flow rate of 1.0 mL/min.The detection was based on the chemiluminescence reaction of repaglinide with acidic potassium permanganate（KMnO₄） and tris（2,2’-bipyridyl）ruthenium（Ⅲ）(Ru（bpy）₃³⁺),which was immobilized on the cationic ion-exchange resin for obtaining high sensitivity and reducing consumption of expensive reagent.