Mass spectra of some deuterated ethanes. II. An empirical method of calculation of the spectra

1968 ◽  
Vol 46 (10) ◽  
pp. 1741-1746 ◽  
Author(s):  
Y. Amenomiya. ◽  
R. F. Pottie

Relative intensities of the C2 fragment ions in deuterated (d1–d5) ethanes have been calculated on a statistical basis from the mass spectrum of C2H6 and have been compared with experimental mass spectra previously reported in Part I. For these calculations we have introduced a correction for the relative probabilities of loss of two hydrogen atoms in addition to weighting factors for the loss of H and D atoms. The isotopic weighting factors have been expressed in terms of power series. By this means satisfactory agreement was obtained between the calculated and experimental mass spectra.This treatment also made it possible to calculate the intensities of doubly charged C2 fragments that appear in the C1 mass spectra. We then estimated the degree of reshuffling of hydrogen atoms prior to C—C bond rupture and obtained calculated mass spectra that were in reasonable agreement with the experimental data for the C1 region of the mass spectrum.Experimental mass spectra have been newly obtained for 1,1-d2 ethane and 1,1,1,2-d4 ethane and are included here for completeness.

1967 ◽  
Vol 22 (4) ◽  
pp. 454-459 ◽  
Author(s):  
K. R. Jennings

Metastable transitions have been observed in the mass spectra of benzene, hexadeutero-benzene, 1,4-dideuterobenzene and 1,3,5-trideuterobenzene using a double-focusing mass spectrometer. Decomposition maps have been obtained for each substance and decomposition reactions leading to the production of all significant fragment ions have been suggested. Metastable transitions of several doubly-charged species were found. Loss if identity by the H and D atoms of the partly-deuterated benzenes was observed in metastable transitions in their mass spectra, indicating that rapid isomerization occurs before fragmentation.


2009 ◽  
Vol 15 (4) ◽  
pp. 497-506 ◽  
Author(s):  
Tomasz Pospieszny ◽  
Elżbieta Wyrzykiewicz

Electron ionisation (EI) and fast atom bombardment (FAB) mass spectral fragmentations of nine 2,4-(and 2,1-) disubstituted o-( m- and p-)nitro-(chloro- and bromo-)-2-thiocytosinium halides are investigated. Fragmentation pathways, whose elucidation is assisted by accurate mass measurements and metastable transitions [EI-mass spectrometry (MS)], as well as FAB/collision-induced dissociation (CID) mass spectra measurements are discussed. The correlations between the abundances of the (C11H10N4SO2)+1–3; (C11H10N3SCl)+4–6 and (C11H10N3SBr)+7–9 ions and the selected fragment ions (EI-MS), as well as (C18H16N5SO4)+1–3; (C18H16N3SCl2)+4–6 and (C18H16N3SBr2) + 7–9 ions and the selected ions (C7H6NO2)+1–3; (C7H6Cl)+ 4–6; (C7H6Br)+ 7–9 (FAB-MS) are discussed. The data obtained can be used for distinguishing isomers.


2003 ◽  
Vol 75 (5) ◽  
pp. 1155-1163 ◽  
Author(s):  
David L. Tabb ◽  
Lori L. Smith ◽  
Linda A. Breci ◽  
Vicki H. Wysocki ◽  
Dayin Lin ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Andreas A. Hildebrand ◽  
Erika Pfeiffer ◽  
Georg Damm ◽  
Manfred Metzler

Recent studies on the mammalian and fungal metabolism of the mycotoxin zearalenone (ZEN) have disclosed the formation of six regioisomers of monohydroxy-ZEN and its reductive metabolite zearalenol (ZEL). Hydroxylation occurs at the aromatic ring or at one of four positions of the aliphatic macrocycle. In addition, an aliphatic ZEN epoxide, its hydrolysis product, and other products were identified in fungal cultures. In this paper, we report the product ion spectra of the [M-H]− ions of 22 oxidative metabolites of ZEN and ZEL, obtained by LC-MS2 analysis using a linear ion trap mass spectrometer with negative electrospray ionization. The MS2 spectra exhibit qualitative and quantitative differences which allow a clear distinction of most metabolites. Moreover, GC-MS analysis of the trimethylsilylated metabolites yields electron impact mass spectra with numerous fragment ions which can be used as fingerprint to confirm the chemical structure derived by LC-MS2 analysis.


1982 ◽  
Vol 17 (1) ◽  
pp. 19-28 ◽  
Author(s):  
A. W. Hanner ◽  
L. E. Abbey ◽  
D. E. Bostwick ◽  
E. M. Burgess ◽  
T. F. Moran
Keyword(s):  

1983 ◽  
Vol 18 (7) ◽  
pp. 282-294 ◽  
Author(s):  
J. R. Appling ◽  
B. E. Jones ◽  
L. E. Abbey ◽  
D. E. Bostwick ◽  
T. F. Moran
Keyword(s):  

1965 ◽  
Vol 20 (7) ◽  
pp. 883-887 ◽  
Author(s):  
J. H. Beynon ◽  
B. E. Job ◽  
A. E. Williams

The mass spectra of benzoic acid, phthalic acid, isophthalic acid and terephthalic acid, together with the analogues deuterated on the carboxylic acid group have been studied. Exchange of the deuterium atom with hydrogen atoms on the positions ortho to a carboxylic acid group on the aromatic ring has been studied using meta-stable peaks.


1989 ◽  
Vol 44 (1) ◽  
pp. 17-20 ◽  
Author(s):  
G. Hagenow ◽  
H.-W. Jochims ◽  
J. Sawatzki ◽  
R. Minkwitz ◽  
H. Baumgärtel

Abstract The ionization potential of CH3SCF3 and the appearance potentials of fragment ions have been measured in the photon energy range 9 -19 eV using synchrotron, radiation. From these results thermochemical data of CH3SCF3, CH3SCF3+ and fragment ions have been evaluated.


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