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A study of rearrangement processes in the mass spectra of substituted diphenyl-ethers

✍ Scribed by J. A. Ballantine; C. T. Pillinger


Publisher
John Wiley and Sons
Year
1968
Tongue
English
Weight
471 KB
Volume
1
Category
Article
ISSN
1076-5174

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✦ Synopsis


An investigation of the mass spectra of a number of substituted diphenyl ethers has shown that the major fragment ions are commonly due to cleavage of the molecule into the two benzene 'half' fragments although in many cases the molecular ion is the most abundant species observed.

Little evidence is seen of M-CO or M 4 H O peaks in these molecules but a large number of different rearrangement processes have been observed which involve ortho-substituents. These rearrangement ions, although in some cases not very abundant, can be diagnostic in the problem of locating substituents in the diphenyl ether nucleus.


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