FAST-ATOM-BOMBARDMENT COMBINED WITH MASS-SPECTROMETRY FOR CHARACTERIZATION OF POLYCYCLIC AROMATIC-HYDROCARBONS

被引:17
作者
DASS, C
机构
[1] Charles B. Stout Neuroscience Mass Spectrometry Laboratory, Department of Neurology, University of Tennessee-Memphis, Memphis, 38163, TN
基金
美国国家卫生研究院;
关键词
D O I
10.1016/1044-0305(90)85021-D
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new approach using fast atom bombardment combined with mass spectrometry to characterize polycyclic aromatic hydrocarbons (PAHs) in the range of 128-252 u molecular weight is described. Sulfolane was employed as a liquid matrix for these π-conjugated hydrocarbons. Bombardment of sulfolane solution of certain PAHs with an atom beam produces both radical cation (M+.) and protonated molecule [(M + H)+], with no evidence of fragmentation. Collisional activation of the fast atom bombardment-desorbed M+. ions, however, results in several structure-specific fragment ions. Structural differences in a few isomeric hydrocarbons can be detected using the [(M + H)+]/[M+.] abundance ratio and in the pyrene-fluoranthene pair by the B/E linked-field-collision-activated dissociation data. The [(M + H)+]/[M+.] was found to be compound-specific and correlated well with certain properties (resonance energy, proton affinity, and ionizing energy) of PAHs. © 1990 American Society for Mass Spectrometry.
引用
收藏
页码:405 / 412
页数:8
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