Stereoselective effects in the solid-phase hydrogenation of unsaturatedl-hydroxyproline derivatives

The solid-phase catalytic hydrogenation of (R-4tert-butoxy-Δ¹-pyrroline-2-carboxylic) acid under the action of hydrogen spillover was studied. The reaction proceeds stereoselectively with the predominant formation of thel-amino acid. The configuration of the asymmetric center formed is determined by that of the asymmetric C(4) atom. The major portion of the isotope label is incorporated into the allylic C(3) and C(5) positions, and the β-H atoms are more mobile. Using quantum-chemical calculations, the geometric structure of thel-hydroxyproline molecule was calculated, and the spin-spin coupling constants for this tritium-labeled amino acid were determined. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1820–1823, October, 1997.     

Flotation-photometric determination of silicon in the form of chromopyrazole II molybdosilicate

The process of concentrating chromopyrazole II alpha- and beta-molybdosilicates by flotation with mixtures of toluene with polar solvents (acetone, ethanol, isoamyl alcohol, cyclohexanol or cyclohexanone) has been studied. It was found that the composition of the complex depends on the acidity of the medium. The complex was isolated from 1.5M sulphuric acid. On the basis of elemental analysis the ratio of chromopyrazole II to molybdosilicate was found to be 2:1. Infrared spectroscopy was used to establish that an ion-association complex is formed. The results were used to establish a method for determination of ultratrace levels of silica (2 mug/l.) in high-purity water. The relative standard deviation is 7-11%.     

关于开设内光电效应实验的探索与思考

介绍了开设以内光电效应为理论基础的半导体光电器件的重要性和迫切性,并详细介绍了内光电效应的理论与半导体光电器件的分类和应用前景。     

关于强Armendariz环和强拟Armendariz环

提出了强拟Armendariz环的概念,给出了强Armendariz环和强拟Armendariz环上的一些结果.     

Incompressible electron phase in field-effect transistors

The formation of regions of compressible and incompressible phases in the quantum Hall effect regime has been considered for a two-dimensional (2D) electron system that is created in a field-effect transistor. This effect arises from long-period fluctuations of the density of ionized donors supplying electrons to the 2D system. It is shown that the motion of these regions caused by variations of the average electron density gives rise to minima in the capacitance of the capacitor formed by the 2D electron system and the transistor gate. When the corrections to the capacitance are small, the shape of the minima reproduces the donor density distribution function. Experimental data are presented that demonstrate good agreement with the predictions of the model.     

非晶硅太阳电池的光伏检测磁共振研究

本文利用光伏检测磁共振(PDMR)方法初步研究了p⁺in⁺ a-Si:H太阳电池中与自旋状态有关的复合机制。研究表明太阳电池的制作工艺不同,相应的PDMR共振信号的线型和g因子亦不同,因而起支配作用的复合过程不同。根据PDMR结果讨论了a-Si:H膜的生长速度、衬底温度、本征层厚度等对太阳电池性能的影响。 关键词：     

Study of the products of platinum-catalyzed hydrogenation of chlorinated nitro and amino aromatic compounds at high degree of dehalogenation

The kinetics of formation and consumption of the dehalogenation products during hydrogenation of 3,4-dichloronitrobenzene under static and gradient-free flow conditions and hydrogenation of p-chloroaniline under static conditions were studied in the presence of platinum supported on active carbon. In the former case, p-chloroaniline and aniline are the primary dehalogenation products; in the presence of the catalyst, they can react with each other giving biphenyl derivatives, whose synthesis and accumulation in the reaction mixture occur with a considerable delay and have not been investigated before.     

Synthesis and structure of new thorium phosphate CaGdTh(PO<Subscript>4</Subscript>)<Subscript>3</Subscript>

Phosphate CaGdTh(PO₄)₃ was prepared by thermal treatment of a mixture of oxides. The final temperature was 1400°C. The phosphate was characterized by powder X-ray diffraction analysis and IR spectroscopy. The crystal structure was studied by the Rietveld method. The compound crystallizes in the monazite structure type (sp. gr. P2₁/n). A comparative analysis of the structures of this phosphate and cerium orthophosphate CePO₄ was carried out.     

Liquid-phase catalytic hydrogenation of 3,4-dichloronitrobenzene over Pt/C catalyst under gradient-free flow conditions in the presence of pyridine

Experimental data on nitro compound uptake, the intermediate product accumulation, and the corresponding amine compound generation were obtained on hydrogenating 3,4-dichloronitrobenzene over Pt/C catalyst in the gradient-free flow regime in the presence and absence of pyridine. In addition, a side reaction of dehalogenation was investigated. The role of pyridine admixture on every step of the process was analyzed and the rate of hydrogenation of the nitro compound was determined both in the presence and in the absence of inhibitor.