Field desorption mass spectrometry of large multiply branched saturated Hydrocarbons

被引:25
作者
Gross, JH
Vékey, K
Dallos, A
机构
[1] Inst Organ Chem, D-69120 Heidelberg, Germany
[2] Hungarian Acad Sci, Inst Chem, H-1025 Budapest, Hungary
[3] Univ Veszprem, H-8200 Veszprem, Hungary
来源
JOURNAL OF MASS SPECTROMETRY | 2001年 / 36卷 / 05期
关键词
field desorption mass spectrometry; hydrocarbons; Apolanes; fragmentation; metastable ion;
D O I
10.1002/jms.151
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Large multiply branched saturated hydrocarbons containing 67-103 carbon atoms (molecular masses 941.8-1446.8 Da) were analyzed by field desorption mass spectrometry (FD-MS) with a double-focusing mass spectrometer. FD-MS was found to have detection limits in the 100 fmol range. The FD mass spectra exhibited molecular ions of astonishingly low abundance. However, the fragment ions formed were closely related to the proposed molecular structure, allowing us to set up rules for straightforward structure elucidation of unknowns. In detail, (i) dehydrogenation, (ii) alkyl losses from molecular ions and (iii) subsequent alkene losses were observed. The influence of the electric field strength on dehydrogenation and C-C cleavages was examined by variation of the emitter potential. Additionally, ion dissociations in the ion source and in the first and second field-free regions, respectively, were compared to study the relative importance of field-induced and thermally induced processes. Copyright (C) 2001 John Wiley gr Sons, Ltd.
引用
收藏
页码:522 / 528
页数:7
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