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Inherent Stability Limits of Intramolecular Boron Nitrogen Lewis Acid-Base Pairs

Inherent Stability Limits of Intramolecular Boron Nitrogen Lewis Acid-Base Pairs

Daniel Winkelhaus, Beate Neumann, Hans-Georg Stammler, Raphael J F Berger, Yuri V Vishnevskiy, Norbert W Mitzel

Chemistry. 2012 Jul 23;18(30):9312-20.

PMID: 22707351

Abstract:

The reaction of (C(6)F(5))(2)BH (1) with N,N-dimethylallylamine (2), N,N-diethylallylamine (3) and 1-allylpiperidine (4) afforded the five-membered ring systems (C(6)F(5))(2)B(CH(2))(3)NR(2) (R = Me (5), Et (6)) and (C(6)F(5))(2)B(CH(2))(3)N(CH(2))(5) (7) with an intramolecular dative B-N bond. A different product was obtained from the reaction of (C(6)F(5))(2)BH (1) with N,N-diisopropylallylamine (8), which afforded the seven-membered ring system (C(6)F(5))(2)B(CH(2))(3)N(iPr)CH(Me)CH(2) (9) under extrusion of dihydrogen. All compounds were characterised by elemental analysis, NMR spectroscopy and single-crystal X-ray diffraction experiments. Density functional theory (DFT) studies were performed to rationalise the different reaction mechanism for the formation of products 6 and 9. The bonding situation of compound 9 was analysed in terms of its electron density topology to describe the delocalised nature of a borane-enamine adduct.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
AP2155944	N,N-Dimethylallylamine		2155-94-4	Price

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