Unimolecular reactions of the metastable silicenium ion (CH,),SiOSi(CH,), + generated by dissociative ionization of hexamethyldisiloxane were investigated by mass-analysed ion kinetic energy (MIKE) spectrometry. The characteristic fragmentations observed were losses of CH, and (CH,),Si=O molecules.
Metastable ion study of organosilicon compounds. Part I—Diethoxydimethylsilane
✍ Scribed by Seiji Tobita; Susumu Tajima; Fumio Okada
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 483 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1076-5174
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✦ Synopsis
Electron impact induced fragmentations of diethoxydimethylsilane (1) and its deuterium-labelled analogues (2 and 3) were investigated by mass-analysed ion kinetic energy spectrometry. The principal fragmentation processes of compound 1 are dominated by silicenium ions which undergo consecutive losses of ethylene and aldehyde molecules. The fragmentations of 1 led to the formation of protonated silanoic acid [CH,Si(OH),I+ and protonated dimethylsilanone [(CH,),Si=OW+, and their unimolecular reactivities were clarified. The fragmentation characteristics of compound 1 are compared with those of the carbon analogue, acetone diethyl acetal(4).
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