Abstract
Tris(silyl)amines with three different silylgroups (7–10) and a difluoroboryl-bis(di-tert-butylfluorosilyl)amine (11) are prepared in the reaction of lithiated bis(silyl)amines (2–6) with fluorosilanes and BF3 In the bulky substituted tris(silyl)amines 9 and 10 a rotational barrier is observed by NMR-spectroscopy at room temperature. An fluorosilyl substituted aminoiminophosphane (12) is obtained in the reaction of lithium-bis(di-tert-butylfluorosilyl)amide (6) with F2PNCMe3SiMe.3 The lithiated bis(silyl)amines 5 and 6 react with PF3 to give the PF2-substituted bis(silyl)amines 13 and 14. Above room temperature 13 forms the cyclodiphosphazene (15) and (CMe3)2SiF2.