Electron impact studies. XI. Mass spectra of aromatic azoxy compounds. Skeletal rearrangement upon electron impact

1967 ◽  
Vol 20 (8) ◽  
pp. 1601 ◽  
Author(s):  
JH Bowie ◽  
RG Cooks ◽  
GE Lewis
Keyword(s):  
Electron Impact ◽  
Mass Spectra ◽  
Molecular Ions ◽  
Skeletal Rearrangement ◽  
Impact Studies ◽  
Azoxy Compounds

The mass spectra of 15 aromatic azoxy compounds are reported and discussed. The spectra exhibit pronounced molecular ions, and fragmentation modes which are produced by both simple cleavage and complex skeletal reorganization processes.

Electron impact studies. XXXII. Negative-ion mass spectra of aromatic compounds containing the =N-O- substituent

1968 ◽  
Vol 21 (8) ◽  
pp. 2031 ◽  
Author(s):  
JH Bowie ◽  
SO Lawesson ◽  
BS Larse ◽  
GE Lewis ◽  
G Schroll
Keyword(s):  
Electron Impact ◽  
Aromatic Compounds ◽  
Mass Spectra ◽  
Molecular Ions ◽  
Negative Ion ◽  
Skeletal Rearrangement ◽  
Marked Contrast ◽  
Azoxy Compounds ◽  
Positive Ion ◽  
Fragmentation Processes

The negative-ion mass spectra of aromatic azoxy compounds, nitrones, and N-oxides exhibit pronounced molecular ions and simple fragmentation processes. No skeletal-rearrangement fragments are produced upon electron impact, in marked contrast to those exhibited in the positive-ion spectra of these compounds.

Electron impact studies. XL. Negative-ion mass spectra of organosulphur compounds : Thioglycollic acids and arylsulphinylamines

1969 ◽  
Vol 22 (1) ◽  
pp. 153 ◽  
Author(s):  
JH Bowie ◽  
F Duus ◽  
S Lawesson ◽  
FCV Larsson ◽  
J+ Madsen
Keyword(s):  
Electron Impact ◽  
Mass Spectra ◽  
Molecular Ions ◽  
Negative Ion ◽  
Skeletal Rearrangement ◽  
Marked Contrast ◽  
Impact Studies ◽  
Positive Ion ◽  
Hydrogen Rearrangement

The negative-ion mass spectra of thioglycollic esters and S- alkylthioglycollic acids exhibit ions produced by simple cleavage and/or cleavage with hydrogen rearrangement. Similar spectra of arylsulphinylamines show pronounced molecular ions together with simple cleavage fragments. No skeletal-rearrangement fragments are present in the negative-ion spectra, in marked contrast with those observed in the corresponding positive-ion spectra.

Electron impact studies. VI. Mass spectra of esters and thioesters. Skeletal rearrangement on electron impact

1967 ◽  
Vol 20 (4) ◽  
pp. 689 ◽  
Author(s):  
JH Bowie ◽  
RG Cooks ◽  
P Jakobsen ◽  
S Lawesson ◽  
G Schroll
Keyword(s):  
Carbon Dioxide ◽  
Carbon Monoxide ◽  
High Resolution ◽  
Electron Impact ◽  
Mass Spectra ◽  
Skeletal Rearrangement ◽  
Unsaturated Esters ◽  
Impact Studies ◽  
Unsaturated Alcohols ◽  
Metastable Ions

The mass spectra of representative series of simple alkyl acetoacetates, alkyl acetothioacetates, and some unsaturated esters derived from unsaturated alcohols or phenols are reported and discussed. The fragmentation schemes have been established by high resolution measurements, appropriate metastable ions, and by deuterium and 18O labelling. Many of the spectra show significant skeletal rearrangement fragments arising from either loss of carbon monoxide or carbon dioxide.

Electron impact studies. XXXVII. Skeletal-rearrangement fragments in the mass spectra of alkyl and aryl isoxazoles

1969 ◽  
Vol 22 (3) ◽  
pp. 563 ◽  
Author(s):  
JH Bowie ◽  
RKMR Kallury ◽  
RG Cooks
Keyword(s):  
Electron Impact ◽  
Mass Spectra ◽  
Skeletal Rearrangement ◽  
Deuterium Labelling ◽  
Isoxazole Ring ◽  
Impact Studies ◽  
Rearrangement Processes

The mass spectra of substituted isoxazoles are reported and discussed. The spectra of isoxazoles are strikingly different from those of oxazoles because the initial fragmentations of isoxazoles involve N-O bond fission. Specific skeletal-rearrangement processes are observed in many spectra, and it is proposed that they proceed through azirine and oxazole intermediates. Certain fragmentations have been studied by deuterium labelling. The hydrogens attached to an isoxazole ring do not randomize with the hydrogens of the methyl and phenyl substituents.

Electron impact studies. XCVI. Negative ion mass spectra of naturally occurring compounds. Nitrophenyl esters derived from long-chain acids andalcohols

1975 ◽  
Vol 28 (5) ◽  
pp. 1011 ◽  
Author(s):  
JH Bowie ◽  
BJ Stapleton
Keyword(s):  
Electron Impact ◽  
Analytical Method ◽  
Mass Spectra ◽  
Molecular Ions ◽  
Negative Ion ◽  
Impact Studies ◽  
Naturally Occurring ◽  
Molecular Anions ◽  
Positive Ion ◽  
Long Chain

The positive ion mass spectra of long-chain alcohols and acids are either devoid of molecular ions or contain such species in low abundance. The negative ion spectra of p-nitrophenyl esters of these compounds exhibit pronounced molecular anions, showing the technique to be a useful analytical method for these classes of compounds.

Electron impact studies. XVIII. Mass spectra of pyridazines, phthalazines, and related compounds

1967 ◽  
Vol 20 (12) ◽  
pp. 2677 ◽  
Author(s):  
JH Bowie ◽  
RG Cooks ◽  
PF Donaghue ◽  
JA Halleday ◽  
HJ Rodda
Keyword(s):  
High Resolution ◽  
Electron Impact ◽  
Mass Spectra ◽  
Molecular Ions ◽  
Prominent Feature ◽  
Substitution Pattern ◽  
Impact Studies ◽  
Metastable Ions ◽  
Fragmentation Patterns ◽  
Related Compounds

The mass spectra of substituted pyridazines, phthalazines, and related compounds are reported and discussed. Molecular ions are a prominent feature of all the spectra, and fragmentation modes may be usefully correlated with both the type of heterocycle and its substitution pattern. Fragmentation patterns have been substantiated by extensive high resolution studies and appropriate metastable ions.

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