How enhanced molecular ions in Cold EI improve compound identification by the NIST library

2015 ◽  
Vol 29 (23) ◽  
pp. 2287-2292 ◽  
Author(s):  
Tal Alon ◽  
Aviv Amirav
1984 ◽  
Vol 57 (5) ◽  
pp. 1013-1022 ◽  
Author(s):  
Robert P. Lattimer ◽  
Robert E. Harris ◽  
Doyle B. Ross ◽  
Hugh E. Diem

Abstract From the results presented here, it is clear that FD-MS and FAB-MS are very effective analytical methods for the identification of organic additives in extracts from rubber compounds. In the examples above, the molecular weight information provided by FD and FAB provided a nice complement to the IR data. In cases where IR could give only a general answer (i.e., a compound class), the mass spectral data provided a very specific compound identification. It is encouraging that all the samples examined gave useful spectra by both FD and FAB analysis. In most cases, the same information was obtained by both techniques. Certain compounds, however, were observed by FD but not by FAB (wax, oil, isocyanurate antioxidant). While FD provided only molecular weight information, FAB also provided fragmentation to aid in the confirmation of component assignments. Both the FD and FAB mass spectra were fairly complex for most of the extracts, but for different reasons. In FD, oil and wax oligomers gave many molecular ions over a wide mass range. FAB spectra, on the other hand, were somewhat cluttered due to the normal background ions produced by the sputtering process. With both techniques, however, the various components in some fairly complex mixtures were readily identified.


2019 ◽  
Vol 31 (2) ◽  
pp. 347-354
Author(s):  
Ksenia J. Margolin Eren ◽  
Alexander B. Fialkov ◽  
Uri Keshet ◽  
Svetlana Tsizin ◽  
Aviv Amirav

1980 ◽  
Vol 77 ◽  
pp. 705-718 ◽  
Author(s):  
Sydney Leach ◽  
Gérald Dujardin ◽  
Guy Taieb
Keyword(s):  

1989 ◽  
Vol 50 (C2) ◽  
pp. C2-237-C2-243 ◽  
Author(s):  
H. VOIT ◽  
E. NIESCHLER ◽  
B. NEES ◽  
R. SCHMIDT ◽  
CH. SCHOPPMANN ◽  
...  

1982 ◽  
Vol 136 (1) ◽  
pp. 25 ◽  
Author(s):  
Aleksandr V. Eletskii ◽  
Boris M. Smirnov

Author(s):  
Eugen Illenberger ◽  
Jacques Momigny
Keyword(s):  

1982 ◽  
Vol 47 (11) ◽  
pp. 2946-2960 ◽  
Author(s):  
Antonín Trka ◽  
Alexander Kasal

Partial EI-mass spectra of 3β-hydroxy- and 3β-acetoxy-5α-cholestanes substituted in positions 5α-, 6β- or 5α,6β- with a hydroxyl group or halogen atoms (fluorine, chlorine, bromine) are presented. The molecular ions of 5α,6β-disubstituted derivatives of 3β-hydroxy-5α-cholestane (or of its 3-acetate) are considerably more stable than the corresponding monosubstituted derivatives if at least one of the pair of the vicinal substituents is chlorine or fluorine. This increase in stability, most striking in 5α- and 6β-fluoro compounds, is explained by the inductive effect.


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