Abstract
The reaction of aminofluorsilanes of the type (R=H,F) (Me 3Si)2N−SiF2R with two moles of ammonia, or of a mono- or dialkylamine, yields the corresponding amino-compounds, e.g. (Me 3Si)2N−Si(F)R−NH2, (Me 3Si)2N−Si(F)R−NHR′ and (Me 3Si)2N−Si(F)R−NR2′ (R′=Me, Et). Analogous products are obtained by reaction of the aminofluorosilanes with lithium salts of amines with bulky organic substituents in a 1 : 1 molar ratio. Alkoxy- and aryloxyaminofluorosilanes are prepared by the reaction of sodium alcoholates and sodium phenolate with (Me 3Si)2N−Si(F2)R (R=H, C2H3, C2H5, C6H5).
The i.r.-, mass-,1H- and19F-NMR spectra of the above compounds are reported.
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1. Mitt.: Chem. Ber.108, 155, 1975; 2. Mitt.: J. Organometal. Chem.85, 141, 1975; 3. Mitt.: J. Organometal. Chem., im Druck.
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Klingebiel, U., Fischer, D. & Meller, A. Synthese neuer Aminofluorsilane, sowie Alkoxylierung von Bis (trimethylsilyl)-amino-fluorsilanen. Monatshefte für Chemie 106, 459–471 (1975). https://doi.org/10.1007/BF01150527
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DOI: https://doi.org/10.1007/BF01150527