Synthesis and characterization of second-order nonlinear optical polyurethane with high thermal stability

A second-order nonlinear optical polyurethane was formed with an X-type multi-dimensional charge-transfer (CT) chromophore (DNPIPDHPI) and 3,3^′-dimethoxy-4,4^′-diphenyl diisocyanate. Simultaneous poling and polymerization and in situ second harmonic generation (SHG) measurement technique was carried on to evaluate the thermal stability of the poling induced orientation. The SHG signal of the poled polymer film was not decay below 150 °C and remains 90% of relative d₃₃ value at 200 °C, which is better than the results reported in literature. Comparison of thermal stability indicates that the X-type chromophores possess better property in controlling the decay of the SHG activity than classic chromophores.     

Bimetallic reactivity. On the use of oxadiazoles as binucleating ligands

Two (1,3,4)-oxadiazole ligands have been prepared. In one case the oxadiazole ring is flanked by two o-aniline groups, and in the other case it is an extension of the first where the amines are condensed with 2-picolyl groups. A monometallic copper(II) complex of the former has been prepared, and its crystal structure was determined. A number of bimetallic copper(II), cobalt(II), and nickel(II) complexes of the di-deprotonated latter ligand were prepared and isolated. The crystal structure of the cobalt(II) complex bearing two acetate bridges is reported. The work demonstrates that the seldom-employed oxadiazole ring can be used effectively for generating bimetallic complexes.     

分解水制氢的KNO3—I2循环之研究：Ⅲ.代替电解反应的一个子循环

本文提出了一个硫酸中间盐子循环用以代替分解水制氢的KNO_3-I_2混合循环中的电解反应,从而使原混合循环变为一个纯热化学循环。     

微量热法研究γ-Mo2N催化剂表面氢的微分吸附热

Differential heats of H 2 adsorption on γ-Mo2N catalysts were studied by using microcalorimetry. Samples with high and medium surface areas (90 and 17 m2•g -1 ) present a homogeneous energetic distribution of surface sites, which corresponds with the preferential orientation of their (200) planes. Molybdenum nitride with low surface area (8 m2•g -1 ) displays a heterogeneous energetic distribution of H 2 adsorption sites. The higher initial differential heat of hydrogen adsorption observed for the low surface Mo nitride was attributed to species adsorbed on surface sites associated with the (111) plane.     

制备方法对Mg1.9Al0.1Ni合金储氢性能的影响

文中采用机械合金化(MA)和氢化燃烧法(HCS)制备了Mg1.9Al0.1Ni,通过对它们储氢性能的对比研究发现,MA优于HCS.采用MA制得的Mg1.9Al0.1Ni储氢合金具有较高的活性和高储氢量,对PCT结果进行计算,得出温度和氢平衡压的关系式.Mg1.9Al0.1Ni(MA)553K时100s内吸放氢量分别为2.67和2.54 mass%H.用XRD方法进行物相分析,表明添加适量Al没有改变Mg2Ni的物相结构,由于MA能够制备出纳米晶粒,使得Mg1.9Al0.1Ni合金具有更好的储放氢动力学性能.     

Hydrogenated polybutadiene–polymethyl methacrylate (HPB–PMMA) block copolymer. I. Synthesis of polybutadiene–polymethyl methacrylate (PB–PMMA) block copolymer

To get hydrogenated polybutadiene-polymethyl methacrylate (HPB-b-PMMA) block copolymer to be used as a compatibilizer for blends of polyolefin/polar polymer, PB-b-PMMA was synthesized by anionic-free radical mechanism transformation polymerization. Selective extraction, gradient elution thin layer chromatography, and oil-oil emulsion separation techniques were tried to attempt to separate the copolymerization products. Hydrogenation of the PB sequence in PB-b-PMMA yielded HPB-b-PMMA. The compatibilizing function of PB-b-PMMA was shown in blending experiments. © 1993 John Wiley & Sons, Inc.     

Rapid—In—situ Determination of Chromium （VI） in Water Using Modified Diphenylcarbazine with Citrate

In recent years, the determination of Cr (VI) has attracted great attention because of its toxicity to human, plants and animals1-5. Usually, in the industrial waste water, the concentration of Cr (VI) is relatively high and should be determined frequently. So, an accurate, quick, and convenient method for the measurement of Cr (VI) in environmental water, as well as in river, lake, sea and tap water, is of great importance. The method for determination of Cr (VI) by diphenylcarbazine …     

Selective bonding of pyrazine to silicon(100)-2x1 surfaces: the role of nitrogen atoms

The covalent binding of pyrazine on Si(100) have been investigated using high-resolution electron energy loss spectroscopy (HREELS) and x-ray photoelectron spectroscopy. Experimental results clearly suggest that the attachment occurs exclusively through the bonding of the two para-nitrogen atoms with the surface without the involvement of the carbon atoms, as evidenced from the retention of the (sp2) C-H stretching mode in HREELS and a significant down shift of 1.6 eV in the binding energy of N 1s. The binding mechanism for pyrazine on Si(100) demonstrates that reaction channels for heteroatomic aromatic molecules are strongly dependent on the electronic properties of the constituent atoms.     

Highly enantioselective hydrogenation of N-phthaloyl enamides

Rh- or Ru-catalyzed highly enantioselective hydrogenation of N-phthaloyl enamides is presented. Electron-rich TangPhos and DuanPhos are found to be effective ligands for Rh-catalyzed hydrogenation of α-aryl enamides and up to 99% ee has been achieved. In contrast, for the hydrogenation of α-alkyl enamide, the Ru-C₃-TunePhos complex is more effective and up to 69% ee can be observed. This work is the first report of the hydrogenation of N-phthaloyl enamides.     

邻苯二甲酸在异丙醇-水混合溶剂中电离热力学性质的研究

The first thermodynamic dissociation constants of o-phthalic acid were determined at five temperatures from 278.15 to 318.15 K in 10, 14.93 and 20 wt% isopropanol-water solvent mixtures, by precise e. m. f. measurements of hydrogen-silver chlorld electrodes in cells without liquid junction. On the basis of Pitzer's theory, the method of polynomial approximation was used to determine the dissociation constants of H_2P and the results obtained were compared with traditional extrapolation according to the extended Debye-Huckel equation Results obtained from both methods agree within experimental error. The dependence of the first thermodynamic dissociation constant on temperature was given as a function of the thermodynamic temperature T by the empirical equation: pK_1=A_0+A_1/T+A_2/T. The thermodynamic quantities of dissociation in the mixed solvents have been calculated, and the results have been discussed.