Cbemical ionization mpss spectra of halomethanes measured using tetramethylsiiaw as reagent gas exhibit three major peaks corresponding to [ M + SiMe,l\*, IM -XI + and (MeSi)lX+ ions (X = C1, Br or I). Dihalomethaws CH,X, form tbe most stable silylated molecular iom, whereas in the mass spectra of t
Tetramethylsilane Chemical Ionization Mass Spectrometry of Mono-substituted Aromatic Compounds: Gas-phase Trimethylsilylation
✍ Scribed by R. Srinivas; A. Rama Devi; G. K. Viswanadha Rao
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 397 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0951-4198
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✦ Synopsis
The tetramethylsilane (TMS) chemical ionization (CI) spectra of the mono-substituted aromatics studied contain M+' and adduct [M + (CH, 1, IS]' ions. Abundant M+' ions are observed in compounds with electrondonating groups and are attributed to charge-exchange reactions of reactant ions in the TMS CI plasma. The stabfity of adduct ions in the halobenzenes was found to increase from fluorobenzene to iodobenzene. A collision-induced dissociation study of the [M + (CH,),Si]' ions of these compounds has been carried out to gain an insight into the site of adduction.
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