Mass spectrometry of quaternary ammoniohexanoates: Intermolecular alkyl transfer during field desorption
โ Scribed by R. A. Sanders; A. J. DeStefano; T. Keough
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 257 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1076-5174
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โฆ Synopsis
Intermolecular alkyl transfer occurs during field desorption of quaternary ammoniohexanoates, resulting in mass spectra containing structurally diagnostic adduct ions. Methyl, ethyl and propyl groups attached to nitrogen readily undergo intermolecular transfer to give [M+CH,]', [M+C,H,]+ and [M+C,H,]+ ions, respectively. Evidence is presented that alkyl groups even as large as CloHz, can transfer intermolecularly at high emitter temperatures. In addition to the alkyl ion adducts, the field desorption spectra of CloH21N(CH3)z(CHz),COO-show several other adduct and fragment ions whose relative intensities depend strongly on emitter current. The field desorption results are compared with earlier pyrolysis electron impact results on similar compounds.
๐ SIMILAR VOLUMES
Fast atom bombardment mass spectrometry (FABMS) of five neat phthalates (dimethyl, diethyl, diallyl, dibutyl and dinonyl) were investigated and intermolecular alkyl transfer reactions were observed in the mass spectra. FABMS of some related compounds was also studied and the results indicate that in