Premium
Beiträge zur Chemie des Bors, 213. Reaktionen eines Amino–imino–borans mit Triboran(7) und Decaboran(14)
Author(s) -
Geisberger Gilbert,
Linti Gerald,
Nöth Heinrich
Publication year - 1992
Publication title -
chemische berichte
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 0009-2940
DOI - 10.1002/cber.19921251212
Subject(s) - decaborane , chemistry , borane , boranes , tautomer , dichloromethane , adduct , medicinal chemistry , molecule , stereochemistry , boron , organic chemistry , catalysis , solvent
Contributions to the Chemistry of Boron, 213 [1] . – Reactions of an Amino–imino–borane with Triborane(7) and Decaborane(14) Triborane(7)‐THF hydroborates ( tert ‐butylimino)(tetramethylpiperidino)borane 1 slowly to form μ‐( tert ‐butylamino)‐μ‐(tetramethylpiperidino)tetraborane(8) 5 . This molecule shows fluxional behaviour at ambient temperature in solution. In the solid state, an X–ray structure analysis reveals the presence of the asymmetric 1104–styx valence tautomer. 1 does not react at ambient temperature with pentaborane(9) in dichloromethane/hexane solution. However, 1 reacts rapidly with decaborane(14) to produce a tetramethylpiperidine adduct of an 11‐( tert ‐butylamino)undecaborane(14) as determined by an X–ray structure analysis. The same kind of reaction occurs between decaborane(14) and (2,6–diisopropylphenylimino)‐(2,2,6,6–tetramethylpiperidino)borane. Thus, decaborane(14) acts as a diprotic acid towards amino–imino–boranes.