首页 | 本学科首页   官方微博 | 高级检索  
     检索      

丙酮肟1H核磁共振溶剂效应的研究
引用本文:张建军,马子川.丙酮肟1H核磁共振溶剂效应的研究[J].波谱学杂志,1995,12(2):179-184.
作者姓名:张建军  马子川
作者单位:1. 河北师范大学实验中心;2. 河北师范学院化学系;3. 河北轻化工学院
摘    要:测定了丙酮肟在四氯化碳、氯仿、二氯甲烷、苯和甲苯溶剂中随丙酮肟摩尔浓度变化的1H NMR谱,观察到在氯代甲烷溶剂中,丙酮肟分子中两个甲基和氯代甲烷的质子共振峰随丙同肟摩尔浓度增加而逐渐移向高场,而羟基共振峰却逐渐移向低场。其两个甲基表现为单峰。在芳烃溶剂中,丙酮肟分子中两个甲基和芳烃质子共振峰随丙酮肟摩尔浓度增加逐渐移向低场,且两个甲基表现为双峰,得到了所有化学位移与丙酮肟摩尔浓度呈线性关系。

关 键 词:1H  NMR  溶剂效应  线性关系  化学位移  
收稿时间:1994-03-21

A STUDY OF THE SOLVENT EFFECT OF ACETOXIME BY ~1H NMR
Zhang Jianjun,Ma Zichuan,Zhang Haifeng.A STUDY OF THE SOLVENT EFFECT OF ACETOXIME BY ~1H NMR[J].Chinese Journal of Magnetic Resonance,1995,12(2):179-184.
Authors:Zhang Jianjun  Ma Zichuan  Zhang Haifeng
Institution:Experimental Center, Hebei Normal University, Shi Jiazhuang 050016;2. Department of Chemistry, Hebei Teachers College, Shi Jiazhuang 050091;3. Hebei Institute of Chemical Technology and Light Industry, Shi Jiazhuang 0
Abstract:1H NMR spectra of acetoxime have been measured as the function of the molar concentration of acetoxime in solvent of carbon tetrachloride,chloroform、dichloromethane、benzene and toluene.It has been found that the chemical shifts of the resonance absorption lines of the two methyl groups in acetoxime and of methine halide move upfield gradually as the molar concentration of acetoxime increascs, but the resonance absorption line of hydroxyl group in acetoxime movc downfield gradually. The absorption line of the two methyl groups in acetoxime shows a singlet.In the solvent of aromatic hydrocarbons, the resonanee absorption lines of the two methyl groups in acetoxime and of aromatic hydrocarbons move downfield gradually as the molar concentration of acetoxime increases, and the absorption line of the two methyl groups in acetoxime splits to a doublet. At the same time, it has been found that all the chemical shifts show linear relation with the molar concentration of acetoxime.
Keywords:1H NMR  Solvent effects  Linear relation  Chemical shifts  
本文献已被 CNKI 维普 等数据库收录!
点击此处可从《波谱学杂志》浏览原始摘要信息
点击此处可从《波谱学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号