Substituent effects in unimolecular ion decompositions. VIII. Rearrangement ions in the mass spectra of substituted phenyl methyl ethers

1968 ◽  
Vol 33 (1) ◽  
pp. 124-127 ◽  
Author(s):  
Fred W. McLafferty ◽  
Maurice M. Bursey
1975 ◽  
Vol 10 (4) ◽  
pp. 295-312 ◽  
Author(s):  
Kenneth E. Richards ◽  
Blair N. McMaster ◽  
Graeme J. Wright

1989 ◽  
Vol 24 (1) ◽  
pp. 41-46 ◽  
Author(s):  
Concetta Kascheres ◽  
Mirtes Sintoni

1972 ◽  
Vol 27 (4) ◽  
pp. 670-677 ◽  
Author(s):  
Steven Benezra ◽  
Maurice Bursey

Abstract Simplified quasi-equilibrium calculations performed on the mass spectra of dihalosubstituted phenyl acetates and acetanilides again uncover the same substituent effects on the rise of K with E for the loss of ketene from phenyl acetates as was determined for the monosubstituted phenyl acetates. However, a new effect is found for the disubstituted acetanilides, removal of excitation probability for low-lying energy states of the molecular ion. This effect parallels the removal of transition probability for the lowest excited state of the neutral molecule.


1968 ◽  
Vol 21 (5) ◽  
pp. 1233 ◽  
Author(s):  
JH Bowie ◽  
GE Lewis ◽  
JA Reiss

The mass spectra of a series of benzo[c]cinnoline derivatives are reported and discussed. The spectra are useful for analytical purposes, as all compounds give pronounced molecular ions, and the fragmentation processes generally occur without skeletal-rearrangement. Many benzo[c]cinnolines which are substituted in the 4-position may be differentiated from other isomers by the presence of "proximity- effects" in their mass spectra.


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