An one-pot epitaxial growth method to synthesize cactus-like ZnO

In this work, we have developed a one-pot, morphology controlled epitaxial growth method to synthesize novel cactus-like ZnO in solution. Utilizing zinc acetate and hexamethylenetetramine as the precursors, ZnO nanorods synthesized in the first step remained in the solution, without any separation, served directly as the matrix for the epitaxial growth in the second step. Control experiments revealed that a proper mass of precursors added in the second step was crucial to form cactus-like ZnO. The as-synthesized ZnO was single crystalline and possessed three photoluminescence emissions centered at 390, 425 and 490 run. Finally, a possible mechanism for the epitaxial growth ZnO was proposed and discussed.

Crystal structure of tris(methylcyclopentadienyl) tetrahydrofuranatosamarium

The first crystal structure of tris(methylcyclopentadienyl) tetrahydrofuranato (THF) lanthanide complexes, (CH3Cp)(3)Sm . THF, is determined. The complex crystallizes from mixed solvents of tetrahydrofuran and hexane as a monomer in the orthorhombic space group Pc2(1)n with the unit cell parameters a = 9.135(2) Angstrom, b = 13.263(2) Angstrom, c = 16.176(3) Angstrom, and Z = 4.

Novel bipolar conjugated polymer containing both triphenylamine and oxadizole units

A novel bipolar conjugated polymer containing triphenylamine and 1, 3, 4-oxadiazole units was synthesized by Suzuki reaction. Its structure and properties were characterized by NMR, IR, UV-Vis, PL spectroscopy and electrochemical measurement. The photo luminescent spectroscopy and cyclic voltammograms measurement demonstrated that the resulting polymer shows blue emission (477 nm) and possesses both electron and hole-transporting property.

Synthesis, characterization and crystal structures of dibenzo-18-crown-6 sodium isopolytungstates

Two novel dibenzo-18-crown-6 sodium isopolytungstates, [(DB18C6)(CH3OH)Na](2)W(6)O(19)(.)DB18C6(.)H(2)O 1 and [(DB18C6)(DMF)(2)Na](4)W(10)O(32)(.)2DMF(.)2H(2)O 2, have been synthesized in mixed methanol and acetonitrile solvents and characterized by elemental analysis, TGA, IR and single crystal X-ray diffraction. The compound 1 crystallizes in the monoclinic space group C2/c with a = 23.182(8), b = 19.527(2), c = 18.737(3) Angstrom, beta = 115.15(2)degrees, V = 7678(3) Angstrom(3), Z = 4, and R1(wR2) = 0.0611(0.1504). The compound 2 crystallizes in the monoclinic space group P21/n with a = 16.516(2), b = 22.325(6), c = 20.425(7) Angstrom, beta = 91.78(2)degrees, V = 7528(3) Angstrom(3), Z = 2, and R1(wR2) = 0.0397(0.0773). The compound 1 exhibits a novel organic-inorganic sandwich-type structure, in which the crown ether-sodium complexes are coordinated to the terminal oxygen atoms of W6O192-. In compound 2, all Na+ ions are thoroughly enveloped into the organic moieties of crown ether and DMF molecules and are connected with the 'naked' polyanions W10O324- via the electrostatic attraction.

仲壬基苯氧基乙酸萃取金属离子

研究了仲壬基苯氧基乙酸在盐酸介质中对 Eu3+ ,Zn2 + ,Cd2 + ,Co2 + ,Ni2 + ,Cu2 + ,Mn2 + ,Mg2 + 等金属离子的萃取行为 ,考察了平衡水相酸度 ,萃取剂浓度等因素对萃取平衡的影响 ,得到了萃取平衡方程 .根据金属离子之间的分离系数值可看出 ,通过控制适当的酸度 ,有可能分离 Eu3+中通常伴生的一些金属离子 ,同时还可能达到 Co2 +与 Ni2 + ,Zn2 +与 Cd2 +等金属离子之间的相互分离

Luminescence centers and valence change of Eu2+ in KCaF3

The nature of the emission centers and the valence change of Eu2+ in KCaF3:Eu2+ depends strongly on preparation conditions. Experimental results show that there are two different d-->f emission bands, located at 425 and 510 nm, respectively. Their origin, relationship, and the effect of doping concentration on them are discussed. A Eu2+-Eu3+ valence change process is proposed. (C) 2000 Elsevier Science Ltd. All rights reserved.

M_2B_5O_9Cl:Eu(M=Ca,Sr,Ba)的真空紫外光谱特性的研究

采用高温固相反应法合成了M_2B_5O_9Cl:Eu(M=Ca,Sr,Ba)中荧光体,测量了荧光体的真空紫外激发光谱,研究了M_2B_5O_9Cl:Eu(M=Ca,Sr,Ba)的真空紫外光谱特性,观察到基质吸收带位于120～200 nm区域,Eu~(2+)离子的5d能级劈裂随着M~(2+)的半径的增加而减小,同时也观察到基质与稀土离子之间存在的能量传递。

Combination of amperometric detector & UV detector for capillary electrophoresis

A new electrochemical cell assembly with the combination of UV and amperometric detector (AD) based on their complementarity was described. A Nafion tubing junction was used to decouple the high voltage from the separation capillary in the rear of on-column UV detector. In this mode, the electroactive and inert compounds could be detected by UV and AD at the same time. Aromatic amines were determined with the UV and the end-column AD detection to evaluate the performances of the cell assembly. Such an improved electrochemical detector could match the capillary with different diameters. By simple adjustment of the screws, the positioning of the working electrode and the detection capillary was easily gained without microscope. It is also very easy to assemble and disassemble the working electrode when needed. (C) 1999 Elsevier Science B.V. All rights reserved.

Preparation of the phosphor BaMgAl10O17 : Eu2+ by the surface diffusion method

A surface diffusion method was proposed and applied to prepare blue phosphor BaMgAl10O17:Eu2+. The results show that, compared with the direct synthesis method by common high temperature solid state, the concentration of Eu2+ in the phosphor BaMgAl10O17:Eu2+ prepared by the surface diffusion method can be greatly reduced owing to the activator Eu2+ ions distributed mainly over the surface of the phosphor. It is possible to reduce the cost of this kind of the luminescent materials with the aid of the surface diffusion method.

Main-chain photosensitive polyamic acids using alkaline aqueous solution as developer

In order to develop photosensitive polyimides (PSPIs) imaged in alkaline aqueous solution, a photosensitive diamine and relevant polymer containing conjugated double bonds in the main chain have been synthesized. The photosensitive characteristics and thermal stability of the polymers were investigated. These polymers possess good thermal stability and sensitivity to UV irradiation, and could be used to form a PSPI resist using alkaline aqueous solution as developer. (C) 1999 Society of Chemical Industry.

表面扩散法制备BaMgAl_(10)O_(17):Eu~(2+)荧光体

本文提出表面扩散法的思想并应用于稀土三基色发光材料中蓝色组份BaMgAl10O17:Eu2＋的制备．结果表明，同直接高温因相法制得的荧光体相比，利用表面扩散法制备的蓝色荧光体BuMgAl10O17：Eu2＋,在相同的发光亮度条件下，激活剂Eu2＋的浓度可以大为降低，从而为降低这类材料的成本提出了依据和可能.

Isothermal and nonisothermal melt crystallization kinetic behavior of poly(aryl ether biphenyl ether ketone ketone): PEDEKK

Isothermal and nonisothermal melt crystallization kinetics of a novel poly(aryl ether ketone), PEDEKK, were investigated by differential scanning calorimetry. Several kinetic analyses were used to describe the crystallization behavior. The activation energies were determined as 425 and 176 KJ/mol for isothermal and nonisothermal crystallization, respectively. The equilibrium melting point T-m(o) was estimated to be 444 degrees C by using the Hoffman-Weeks approach. The observed crystallization characteristics of PEDEKK were compared with those of the other members of the poly(arpl ether ketone) family.

Synthesis and properties of two series of H-bonded and non-H-bonded thermotropic liquid crystal monomers

Two series of monomers, namely n-1-bromo-(4-(4-nitrophenylazo)phenyloxy]alkanes (Bn, n = 2, 3, 4, 5, 6, 8, 10) and N-n-[4-(4-nitrophenylazo)phenyloxy]alkyl diethanolamines (Cn, n = 3, 5, 6, 10), were synthesized and characterized. Their thermal behaviour was studied by differential scanning calorimetry (DSC), wide angle X-ray diffractometry (WAXD) and polarizing optical microscopy (POM) equipped with a hot stage. The results showed that the Bns (n greater than or equal to 6) exhibit monotropic nematic liquid crystalline behaviour; no liquid crystalline phase was found for the Bns (n < 6), while for the Cns, enantiotropic smectic liquid crystallinity for n = 5, 6, 10 was seen, and for n = 3 monotropic smectic phases were found. This different phase behaviour between Bn and Cn compounds is attributed to their different end groups. The FTIR analysis of Cn indicated that there exists an intermolecular hydrogen bond between hydroxy groups, so that more stable liquid crystalline phase are formed. The effect of the length of the flexible chain on the thermal behaviour is also discussed.

新型有机二硫化物电池正极材料的研究进展

综述了有机二硫化物正极材料的发展过程。有机二硫化物可以用作锂二次电池的正极活性材料，在充电过程中，－ＳＨ氧化而生成Ｓ－Ｓ作为储能官能团；在放电过程中，Ｓ－Ｓ断裂还原成－ＳＨ，完成化学能向电能的转化。有机二硫化物正极活性材料具有非常高的比能量，但必须在高温下工作。用聚苯胺与有机二硫化物复合，形成新的复合正极活性材料，在常温下即获得良好的性能，以０．１ｍＡ／ｃｍ２的电流密度放电，正极的比能量达到６００Ｗｈ／ｋｇ以上。其中，聚苯胺不仅作为活性材料，而且起到电化学催化剂的作用。