Mass spectra of ten %substituted permethylated trisilanes which include compounds with halo, phenyl and hydrido substituents are reported. Labelling with a C03 group disclosed that a terminal silicon is more favourable as a charge position for the trisilyl cation than the middle atom and that a-and
The mass spectra of substituted 2-methylbenzophenones
โ Scribed by James Grimshaw; Charles S. Sell; Reginald J. Haslett
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 288 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1076-5174
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โฆ Synopsis
Abstract
The mass spectra of some methoxy and methyl derivatives of 2โmethylbenzophenone have been examined. Loss of a substituents from 3โฒโand 4โฒโpositions as well as the previously known loss from 2โฒโpositions are important fragmentation processes. Thus, these fragmentations are of little use in locating substituents on benzophenones of unknown structure. Deuterium labelling shows the [M โ 1]^+^ ion from 3โฒ,4,4โฒ,5,5โฒโpentamethoxyโ2โmethyl benzophenone to be due largely to loss of hydrogen from 2โฒโ and 6โฒโpositions.
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