帮助 本站公告
您现在所在的位置:网站首页 > 知识中心 > 文献详情
文献详细Journal detailed

丙酮肟^1H核磁共振溶剂效应的研究
A STUDY OF THE SOLVENT EFFECT OF ACETOXIME BY ~1H NMR

作  者: ; ; ;

机构地区: 河北师范大学

出  处: 《波谱学杂志》 1995年第2期178-183,共6页

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 ̄1HNMR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。 1H NMR spectra of acetoxime have been measured as the function of the molarconcentration of acetoxime in solvent of carbon tetrachloride,chloroform、dichloromethane、benzene and toluene.It has been found that the chemical shifts ofthe resonance absorption lines of the two methyl groups in acetoxime and of methinehalide move upfield gradually as the molar concentration of acetoxime increascs, butthe resonance absorption line of hydroxyl group in acetoxime movc downfield gradual-ly. 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 twomethyl groups in acetoxime and of aromatic hydrocarbons move downfield graduallyas the molar concentration of acetoxime increases, and the absorption line of the twomethyl groups in acetoxime splits to a doublet. At the same time, it has been foundthat all the chemical shifts show linear relation with the molar concentration ofacetoxime.

关 键 词: 溶剂效应 线性关系 化学位移 丙酮肟

领  域: [理学] [理学] [理学] [理学]

相关作者

相关机构对象

相关领域作者

作者 刘广平
作者 彭刚
作者 杨科
作者 陈艺云
作者 崔淑慧