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

用Fourier变换质谱研究苯胺衍生物的自身化学电离
引用本文:方一苇,Giam,C.S.用Fourier变换质谱研究苯胺衍生物的自身化学电离[J].化学学报,1988,46(5):507-509.
作者姓名:方一苇  Giam  C.S
作者单位:美国匹兹堡大学公共卫生研究生院
摘    要:报导了3-苯甲酰氧基苯胺和P-溴代苯胺在FT质谱中的自身化学电离, 采用多共振离子消除技术研究离子-分子反应机理. 着重探讨系列离子m/z 200, 290, 380和470的生成机理.

关 键 词:苯胺P  质谱法  溴代烃  羧酸酯  苯甲酸P  化学电离源质谱法  付里叶变换  

Self-chemical ionization of substituted aniline compounds with Fourier transform mass spectrometry
FANG YIWEI,Giam,C.S.Self-chemical ionization of substituted aniline compounds with Fourier transform mass spectrometry[J].Acta Chimica Sinica,1988,46(5):507-509.
Authors:FANG YIWEI  Giam  CS
Abstract:The self-chem. ionization in Fourier transform mass spectrometry of 3-benzyloxyaniline (I) and p-bromoaniline (II) is reported. A delay time up to 500 ms at 5 ?10-8 Torr is sufficient to permit ion-mol. reactions to take place. I produced the m/z 290, 380 and 470 ions. II produced the m/z 184 ions. The studies of the reaction mechanisms were performed by multiple resonance ion ejection. In the m/z 290, 380 and 470 ions were obtained by reacting the m/z 91, 290 and 380 ions with neutral mols., resp. II produced the ion m/z 184, which were obtained from the reaction of m/z 92 ions with neutral mols., and most possible structure of ion m/z 184 may be H2NC6H4C6H4NH2.
Keywords:BENZAMINE P  MASS SPECTROGRAPHY  BROMOHYDROCARBON  CARBOXYLIC ACID ESTER  BENZENECARBOXYLIC ACID P  CHEMICAL IONIZATION SOURCE MASS SPECTROMETRY  FOURIER TRANSFORM
本文献已被 CNKI 等数据库收录!
点击此处可从《化学学报》浏览原始摘要信息
点击此处可从《化学学报》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