4-氯-4''''-取代-苯丁酮的低能电子轰击质谱和取代基效应的研究

用离子动能谱探讨了9个苯环上不同取代基的4-氯-4′-取代-苯丁酮EI断裂的主要途径是:分子离子先进行Mclafferty重排,而后α-断裂。将电子能量降低至20e v,对Mclafferty重排的产物离子的α-断裂反应用Hammett方程处理,得回归线性方程lgZ/Z_0=-0.37σp-0.008,线性相关系数为0.9949。由此可明显地看出质谱中单分子断裂反应的取代基效应。     

Photolysis of a methanolic solution of benzyl acetate in low acoustic fields

The influence of low acoustic fields on the photolysis of benzyl acetate in solution was investigated. A change in the contributions of alternative photolysis mechanisms is caused by destruction of solvate shells.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 180–181, January, 1995.This study was financially supported by the Russian Foundation for Basic Research (Project No. 93-02-18102).     

Phase separation of poly(γ-benzyl L-glutamate) to liquid crystal and isotropic solution in various helicogenic solvents

Solvent effects on the phase separation of poly(-benzyl L-glutamate) to liquid crystal and isotropic solution have been observed in various helicogenic solvents. The temperature-composition phase diagrams have been determined for each solution. The critical concentrations, ₂ ^* , at which the phase separation occours have been compared in various solvents. In dimethylformamide in which the polymer is molecularly dispersed, the observed ₂ ^* value has agreed with that calculated by Flory's theory. In some solvents in which the polymer aggregates in a head-to-tail mode such as chloroform, the observed ₂ ^* values have been considerably small. It is assumed that the polymer aggregates behave as longer particles than the original particles. In dioxane in which the polymer aggregates highly both in a head-to-tail and a side-by-side modes, the ₂ ^* value has been a little larger than that in chloroform. In this case the relationship between the aggregation and the liquid crystal formation is so complicated that further investigation is necessary. In aromatic solvents such asm-cresol that dissolves the polymer almost molecularly, the ₂ ^* is smaller than that in dimethylformamide. Therefore, the intermolecular interactions between the phenyl groups in the side groups of the polymer and those in solvent molecules must be considered.The author is grateful to Mr. K. Sano and Mr. M. Watanabe for their observation of the liquid crystal formation.     

相转移催化合成增塑剂BBP和水杨醛的研究

相转移催化合成增塑剂ＢＢＰ和水杨醛的研究郭锡坤，高文华，曾东宇（汕头大学化学系，汕头５１５０６３）关键词相转移催化，季铵盐，聚乙二醇，邻苯二甲酸丁苄酯，水杨醛，增塑剂邻苯二甲酸丁苄酯（增塑剂ＢＢＰ）是一种优良的增塑剂．邻羟基苯甲醛（水杨醛）不仅是重要...     

Composition of <Emphasis Type="Italic">Carlina acanthifolia</Emphasis> Root Essential Oil

The root of Carlina acanthifolia All. (Asteraceae) contained 1.0% of essential oil (expressed in g per 100 g of dried plant material). Using GC and GC/MS, nine components were identified (100% of total oil). The structure of benzyl 2-furylacetylene (carlina oxide), which is the principal component of the oil (91.5%), was spectrometrically identified. __________ Published in Khimiya Prirodnykh Soedinenii, No. 4, pp. 331–332, July–August, 2005.     

Carbonylation of Benzyl Halides Over Two-Phase Catalyst of Iron Pentacarbonyl

Carbonylation of benzyl halides to phenylacetic acid was studied in a two-phase system with iron pentacarbonyl as the catalyst precursor. The solutions consisted of a benzyl halide and iron pentacarbonyl in benzene and tetrabutylammonium hydrogen sulfate in aqueous sodium hydroxide. Stirring under carbon monoxide readily produced phenylacetic salts in aqueous phase which were then acidified and extracted with ether. The yields of phenylacetic acid from benzyl iodide and from benzyl bromide were similar at a evel of about 50percnt;, that of the latter being higher by 1%. The yield from benzyl chloride was far less, at a level of only 21%. The rate as studied with gas chromatography was found to decrease in the order benzyl iodide>benzyl bromide>benzyl chloride.     

Polystyrene-supported Benzyl Selenide: An Efficient Reagent for Highly Stereocontrolled Synthesis of Substituted Olefins

Solid-phase methodology has been rapidly and extensively applied to the preparation of small organic molecules recently1. It might be argued that selenoxide syn-elimination provided the principal impetus for the development of organoselenium chemistry. In addition, the required selenoxides are readily available from the oxidation of the corresponding selenides, which in turn can be prepared by the reaction of selenium-stabilized carbanions with various electrophilic substrates2. However, or…     

New selective O-debenzylation of phenol with Mg/MeOH

Carboxylate-benzyl and nitro-benzyl groups used in phenols protection were selectively debenzylated with 3-25 equiv of Mg in methanol at room temperature. Good yields of the desired phenols were obtained within 3-10 h from a wide variety of O-(carboxylate-benzyl)- or O-(nitro-benzyl)-phenols. Selective O-debenzylation was possible in the presence of O-(carboxylate-benzyl)- or O-(nitro-benzyl)-phenols with Mg/MeOH.