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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/2245


    Title: Mass spectra of nitro-,-dihalostyrenes
    Authors: Shaw-Tao Lin;Chun-Jen Lee;Li-Chwen Chen;Keh-Feng Huang
    Contributors: 保健營養生技學系
    Date: 2004-03
    Issue Date: 2009-11-03 05:51:41 (UTC+0)
    Abstract: The electron ionization (EI) fragmentation of nitro-,-dihalostyrenes depends strongly on the specific halogens present as well as on the position of the nitro group. ,-Difluorostyrenes yielded mainly fluoroacetylene ions as the base peaks and o-nitro-,-dihalostyrene possibly furnished the ion with a structure similar to that of benzo[a]isoxazole (11). The structural identity of the ion was verified by comparing the collision-induced dissociation (CID) spectra of m/z 119 ions from p- and o-nitro-,-difluorostyrene, o-nitro-,-dibromostyrene and compound 11.
    Relation: Rapid Communications in Mass Spectrometry 18(9):935 - 938
    Appears in Collections:[Department of Food Nutrition and Healthy Biotechnology] Journal Article

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