Volume 18, Issue 35
Organoelement Compounds
Full Access

ChemInform Abstract: Boron Compounds. Part 75. N-Substituted 4,5-Diethyl-2,5-dihydro-2,2,3-trimethyl-1,2,5-azasilaboroles. Preparation and Characterization.

R. + KOESTER

R. + KOESTER

MPI Kohlenforsch., D-45470 Muelheim/Ruhr, Germany

Search for more papers by this author
G. SEIDEL

G. SEIDEL

MPI Kohlenforsch., D-45470 Muelheim/Ruhr, Germany

Search for more papers by this author
R. BOESE

R. BOESE

MPI Kohlenforsch., D-45470 Muelheim/Ruhr, Germany

Search for more papers by this author
B. WRACKMEYER

B. WRACKMEYER

MPI Kohlenforsch., D-45470 Muelheim/Ruhr, Germany

Search for more papers by this author
First published: September 1, 1987

Abstract

Starting with the sodiumborate (I) the alkali metal 1,2,5-azoniasilaboratoles (V) are obtained via (III).

ChemInform Abstract

Starting with the sodiumborate (I) the alkali metal 1,2,5-azoniasilaboratoles (V) are obtained via (III). Elimination of ethane forms (VI). From (VIa) the NH compound (IX) and NMe compound (VIII) is prepared. (VIa) reacts also with a series of chlorides to yield the N-substituted products (XII)-(XV). Transamination reactions of (VIII) with primary amines and diamines produce the derivatives (XVI)and (XIX), respectively. (VIII) and monoorganohydrazines react under transamination to give mixtures of (XXI) and the isomeric diazasilaborines (XXII) and (XXIII). The compounds are characterized by IR, NMR and mass spectroscopic data. The structure of (XIVa) is determined by an X-ray analysis (space group P21/c, Z=2).

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.