四种三唑化合物的合成及它们在盐酸介质中对碳钢缓蚀性能的研究

本文通过“点击化学”的方法合成了四种1,2,3-三唑化合物(3a, 3b, 4a和4b)，通过IR, ¹H NMR, ¹³C NMR 和 single crystal X-ray 晶体结构衍射分析对化合物进行了表征。通过交流阻抗和动电位扫描极化曲线研究四种化合物在1 mol/L HCl 中对碳钢的缓蚀性能。研究结果表明，四种化合物均可作为高效阳离子缓蚀剂，其中化合物4b的缓蚀效果最好，最高抑制效率可达97％。     

Preparation and evaluation of ammonia decomposition catalysts by high-throughput technique

The high-throughput technique has been successfully employed to investigate systematically NH₃ decomposition catalysts for COx-free hydrogen production. Supported γ-Mo₂N catalysts not only could be prepared and evaluated by the high-throughput experiment, but are also active for NH₃ decomposition luke supported Ni and Co catalysts. Additionally, the preparation process and support play important roles on the catalytic performance of supported γ-Mo₂N catalysts.     

Construction of Ka-Band Preselected Harmonic Mixer

In this paper, a new method to realize pre-selected harmonic mixer is introduced. It includes a harmonic mixer, and a YIG turning filter (YTF) design. A digital driver is used for YTF, which can realize linearization modification and temperature compensation. The spectrum analyzer's out scanning voltage is given an A/D conversion and interface to digital driver.     

HYPERBOLIC-PARABOLIC CHEMOTAXIS SYSTEM WITH NONLINEAR PRODUCT TERMS

We prove the local existence and uniqueness of week solution of the hyperbolic-parabolic Chemotaxis system with some nonlinear product terms. For one dimensional case, we prove also the global existence and uniqueness of the solution for the problem.     

The Synthesis of 2‐(Chromon‐2/3‐yl)‐3‐(5‐thione‐4‐hydro‐1,3,4‐thiadiazol‐2‐yl)‐4‐oxo‐thiazolidine

2‐Formylchromones and 3‐formylchromones as the first materials singly reacted with 2‐amino‐5‐mercapto‐1,3,4‐thiadiazole to give the corresponding Schiff bases, which on cyclocondensation with mercapto‐acetic acid in 1,4‐dioxane yielded target compounds named 4‐oxo‐thiazolidines. The structures of all the synthetic compounds were confirmed by elemental analysis and IR, ¹H NMR, LC‐MS (ESI) spectral data.     

算子权移位的换位代数的交换性

令T是以{Wk}∞k=1B(Cn)为权序列的内射算子权移位.设T是强不可约的,而且sup1k<∞‖W-1k‖< ∞.用A′(T)表示T的换位代数,radA′(T)表示A′(T)的Jacobson根.本文刻划了radA′(T)并且证明了商代数A′(T)/radA′(T)是交换的.     

信息技术与大学数学课程整合的方式与理论探讨

信息技术与大学数学课程整合正成为当前我国信息技术教育乃至整个教育信息化进程中的一个热点问题,探讨其整合的方式及理论基础是非常必要的.本文首先结合大学数学案例探讨了整合的三种方式:动态的课堂演示型、单机的数学实验型和全交互的网络教学型,其次探讨了整合所依据的四种理论:传播理论、建构主义理论、教学设计理论和系统理论,最后提出了自己对信息技术与大学数学课程整合的一些思考.     

Half‐titanocene complexes bearing dianionic 6‐benzimidazolylpyridyl‐2‐carboximidate ligands: Synthesis,characterization, and their ethylene polymerization

6‐Benzimidazolylpyridyl‐2‐carboximidic half‐titanocene complexes, Cp′TiLCl (Cp′ = C₅H₅, MeC₅H₄, C₅Me₅, L = 6‐benzimidazolylpyridine‐2‐carboxylimidic, C1–C13 ), were synthesized and characterized along with single‐crystal X‐ray diffraction. The half‐titanocene chlorides containing substituted cyclopentadienyl groups, especially pentamethylcyclopentadienyl groups were more stable, while those without substituents on the cyclopentadienyl groups were easily transformed into their dimeric oxo‐bridged complexes, (CpTiL)₂O ( C14 and C15 ). In the presence of excessive amounts of methylaluminoxane (MAO) or modified methylaluminoxane (MMAO), all half‐titanocene complexes showed high catalytic activities for ethylene polymerization. The substituents on the Cp groups affected the catalytic behaviors of the complexes significantly, with less substituents favoring increased activities and higher molecular weights of the resultant polyethylenes. Effects of reaction conditions on catalytic behaviors were systematically investigated with catalytic systems of mononuclear C1 and dimeric C14 . With C1 /MAO, large MAO amount significantly increases the catalytic activity, while the temperature only has a slight effect on the productivity. In the case of C14 /MAO catalytic system, temperature above 60 °C and Al/Ti value higher than 5000 were necessary to observe good catalytic activities. In both systems, higher reaction temperature and low cocatalyst amount gave the polyethylenes with higher molecular weights. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3396–3410, 2008