Beiträge zur Chemie der Silicium-Stickstoff-Verbindungen. CV. Ringschlußreaktionen mit 1,5-Bis(alkylamino)trisildioxanen |
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Authors: | F. Rabet U. Wannagat |
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Abstract: | 1.5-Bis(methylamino)hexamethyltrisildioxane reacts in the presence of triethylamine easily with germanium tetrachloride (equ. 1) and ethyldichlorophosphine (equ.2) to give the formerly unknown inorganic eightmembered ring systems Si3GeN2O2 and Si3PN2O2. Respectively. By analogous reacting of silicon tetrachloride only open chained Cl3Si? Nme? Sime2? O? Sime2? O? Sime? NHme (IV; equ. 3) is formed. With metallated 1.5-bis(alkylamino)trisildioxanes, dischlorodiorganylsilanes do not give the expected asymmetric-, but the symmetric cyclotetrasildioxdiazanes V–VII. Dichlorophenylborane, in an analogous reaction, leads to the novel eightmembered ring system BSi3N2O2, but the exact position of the N and O atoms in the ring could not be fixed beyond any doubt. The novel sixmembered ring system BSi2Ni2O was realized in compound IX via equ. (6). |
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