KI与无机铵盐催化CO2与环氧丙烷合成碳酸丙烯酯

以无毒、合成简单、廉价的无机铵盐(氨基甲酸铵、碳酸氢铵、碳酸铵等)为助催化剂,研究其对卤化钾(KCl、KBr、KI)催化CO2与环氧丙烷合成碳酸丙烯酯(PC)的影响.结果表明,卤化钾与无机铵盐显示出很好的协同催化效应.其中以氨基甲酸铵为助催化剂,KI为主催化剂时,催化合成PC的效果最好.同时考察了催化剂用量、反应温度、CO2初始压力、PC的预加入量、反应时间等因素对反应的影响.在优化条件下,PC收率大于99%.     

Structural and magnetic properties of self assembled Fe-doped Cu2O nanorods

Cuprous oxide (Cu₂O) nanorods doped with iron impurities have been synthesized by the polyol method using sodium dodecyl sulfate as the surfactant. The X-ray diffraction measurement reveals the pure phase of simple cubic Cu₂O and the electron microscopy displays its one dimensional morphology. Ferromagnetism was observed at room temperature in the magnetic measurements of the doped samples while undoped sample exhibits only diamagnetism. Room temperature Mössbauer spectra for the samples exhibited only doublets but no sextet, which corresponds to the presence of paramagnetic iron sites. As magnetic moment contribution of the doped ions was insignificant for the observed magnetism, ferromagnetic property in the doped samples could have been originated from the defects as cation vacancies. Existence of the defects was supported by the room temperature photoluminescence spectra of the doped samples in reference to the undoped sample.     

导电聚苯胺/TiO_2微/纳米球的制备及其结构表征

采用具有八面体形貌的氧化亚铜为模板,制备了聚苯胺/TiO2(PANI/TiO2)微/纳米球,TiO2纳米粒子很均匀地分散在聚苯胺中.研究了不同TiO2/苯胺(TiO2/ANI)摩尔比对PANI/TiO2复合物的结构、形貌和电学性能的影响.实验结果表明,随着TiO2/ANI摩尔比的增加,PANI/TiO2复合物的直径逐渐减小,当TiO2/ANI摩尔比为0.16时,复合物的平均直径为373nm,而当TiO2/ANI摩尔比增加到1.6时,复合物的平均直径降到80nm.PANI/TiO2复合微/纳米球的电导率随着TiO2/ANI摩尔比的增加先升高后降低,当TiO2/ANI摩尔比达到1.6时,电导率由10-4S/cm提高到100S/cm,达到最大值.产物的形貌和结构分别采用扫描电镜、透射电镜、红外吸收光谱和X-射线衍射等手段进行了表征.     

Short-living absorption and emission of CsI(Na)

This paper investigates the short-living absorption and the emission of CsI(Na) under a pulsed electron beam (Е_e=0.25 MeV, t_1/2=15 ns and W=0.003…0.16 J/cm²). The bands of singlet self-trapped excitons, as well as Na⁰ and V_k color centers have been detected in the transient absorption spectrum of CsI(Na). It has been found that the activator luminescence spectrum, peaking at 3.0 eV, fits a Gaussian (E_m=3.0 eV and FWHM=0.44±0.02 eV at 80 K) and remains the same at different time delays within 10⁻⁸-10⁻³ s. The decay kinetics of the 3.0 eV emission has one nanosecond exponential component and two microsecond ones with time constants 1.0 and 3.0 μs, which remain unchanged within 78-150 K. It is concluded that the activator emission is due to the radiative annihilation of sodium-perturbed two halide excitons from the non-relaxed singlet state. The pathways of such excitons creation are discussed.     

Mild and efficient oxy-iodination of alkynes and phenols with potassium iodide and tert-butyl hydroperoxide

An efficient synthesis of 1-iodoalkynes and iodophenols was easily achieved by employing simple KI and TBHP. The reaction does not involve the use of a metal and base combination. A variety of substituted alkynes and phenols were prepared with good to excellent yield.     

State of Water in Hydration Spheres of Potassium Iodide

Ion hydration has been studied for potassium iodide solutions with concentrations from 0 to 51 wt.% at temperatures from 288.15 to 308.15 K based on ultrasonic measurements and molar adiabatic compressibility data. For hydration complexes, structural characteristics have been determined. The structure of noncoordinated water plays a significant role even in concentrated solutions. An electrostatic ion field has a strong effect on the temperature dependence of the molar volume of hydration water. A method for the precise determination of the total solvation boundary is presented.     

Synthesis and Crystal Structure of 3,5-Dicyano-2,6-diethylthiopyridine

3,5-Dicyano-2,6-diethylthiopyridine has been synthesized by the alkylation of cyanothioacetamide with ethyl iodide in DMF and its molecular and crystal structures have been investigated. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1351–1354, September, 2005.     

Neue quaternäre Chalkogenohalogenide

The quaternary chalcogeno halides AgHgSI, AgHgSBr and CuHgSI have been synthesized by annealing mixtures of silver (copper) halides and mercury sulphide. AgHgSI decomposes peritectoidally at 593±3 K and crystallizes in the orthohombic system with lattice constants ofa=772.3 (3),b=847.7 (3) andc=707.3 (3) pm. The phase diagram AgI-HgS resembles the AgI-Ag₂S system closely. Contrary to the literature the only stable compound in this system is AgHgSI. The previously mentioned Ag₂HgSI₂ is metastable. The reported compound Ag₂HgSBr₂ could not be synthesized. The substitution of Hg²⁺ by Cd²⁺ in CuHgSI leads to a red phase Cu₂Cd₃S₂I₄ which crystallizes in the wurtzite type structure with lattice parameters ofa=424.7 (1) andc=695.2 (1) pm.