Nucleophilic Addition of Aliphatic Diamines NH2(CH2)nNH2 (n = 6, 9) to Nitrilium Derivatives of the closo-Decaborate Anion [2-B10H9NCR]– (R = CH3, C2H5, nC3H7)

Author:

Voinova V. V.1,Selivanov N. A.1,Bykov A. Yu.1,Klyukin I. N.1,Zhdanov A. P.1,Zhizhin K. Yu.1,Kuznetsov N. T.1

Affiliation:

1. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Abstract

The reaction of a number of nitrilium derivatives of the closo-decaborate anion with hexamethylene- and nonamethylenediamine has been studied. It has been shown that the process proceeds with the functionalization of both amino groups of the nucleophile to form amidines of the type (Bu4N)2[B10H9NH=C(R)NH (CH2)nNH(R)C=NHB10H9] (R = CH3, C2H5, nC3H7; n = 6, 9). Target compounds have been characterized by high resolution multinuclear NMR and ESI mass spectrometry.

Publisher

The Russian Academy of Sciences

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