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- W1527791173 abstract "A series of silylamines (aminosilanes) have been converted into their borane adducts using (tetrahydrofuran)- or (dimethyl sulfide)-borane as the BH3 source. Most of the adducts are unstable in solution and undergo rapid Si-N cleavage to give silanes and aminoboranes. Together with Me3SiNMe2-BH3 the complexes with aziridinyl- and azetidinylsilanes are the most stable. A crystal structure investigation of Ph3Si-N(CH2)2-BH3 has shown that the molecular geometry of the silylamine component of the adduct is virtually identical with that of the free silylaziridine with its steeply pyramidal configuration at nitrogen." @default.
- W1527791173 created "2016-06-24" @default.
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- W1527791173 date "2005-07-26" @default.
- W1527791173 modified "2023-10-03" @default.
- W1527791173 title "Formation, Stability and Structure of Aminosilane-Boranes" @default.
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- W1527791173 doi "https://doi.org/10.1002/9783527620777.ch31c" @default.
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