Extremely bulky secondary phosphinoamines as substituents for sterically hindered aminosilanes

Tobias Bottcher, Cameron Jones

Research output: Contribution to journalArticleResearchpeer-review

10 Citations (Scopus)

Abstract

The synthesis of a series of extremely bulky secondary amines with a phosphine function, Ar†(PR2)NH (Ar† = C6H2{C(H)Ph2}2Pri-2,6,4; R = Ph, NEt2, NPri2) is described. Deprotonation with either n-BuLi or KH yields the respective alkali metal amides in some cases. Their reaction with the chlorosilanes SiCl4, HSiCl3, Cl2SiPh2, Cl3Si–SiCl3 and Si5Cl10 allows access to monomeric molecular compounds bearing the extremely bulky amino substituents via salt elimination. The products obtained may serve as precursors for subsequent reduction reactions to access sterically protected low valent and low coordinate silicon compounds
Original languageEnglish
Pages (from-to)14842-14853
Number of pages12
JournalDalton Transactions
Volume44
Issue number33
DOIs
Publication statusPublished - 2015

Cite this