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)

被引：0

作者：

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
]}

机构：

[1] Russian Acad Sci, Kurnakov Inst Gen & Inorgan Chem, Moscow 119991, Russia

来源：

RUSSIAN JOURNAL OF INORGANIC CHEMISTRY | 2023年 / 68卷 / 10期

关键词：

closo-decaborate anion; amidines; polyfunctional nucleophiles; CARBOXYLIC-ACIDS; METHANE; DODECABORATE; ESTERS; ROUTE;

D O I：

10.1134/S0036023623601885

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

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)(n)NH(R)C=NHB10H9] (R = CH3, C2H5, (C3H7)-C-n; n = 6, 9). Target compounds have been characterized by high resolution multinuclear NMR and ESI mass spectrometry.

引用

页码：1343 / 1348

页数：6

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