Nucleophilic addition of alcohols to the C-N multiple bonds of the nitrilium substituent in the anion [2-B10H9(Naparts per thousandCMe)]-

被引:25
作者
Zhdanov, A. P. [1 ]
Lisovsky, M. V. [1 ]
Goeva, L. V. [1 ]
Razgonyaeva, G. A. [1 ]
Polyakova, I. N. [1 ]
Zhizhin, K. Yu. [1 ]
Kuznetsov, N. T. [1 ]
机构
[1] Russian Acad Sci, NS Kurnakov Gen & Inorgan Chem Inst, Moscow 119991, Russia
基金
俄罗斯基础研究基金会;
关键词
organoboranes; boron-containing cluster anions; addition to carbon-nitrogen multiple bonds; NEUTRON-CAPTURE THERAPY; CHEMISTRY;
D O I
10.1007/s11172-009-0234-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reactions of salts of the anion [2-B10H9(Na parts per thousand CMe)](-) with aliphatic alcohols ROH (R = C (n) H2n+1 (n = 1-6) CH2CH2(OEt), Pr-i, Bu-i, Bu-t, i-C5H11) are studied. These reactions result in hydrolytically stable imidates [2-B10H9{NH=C(OR)Me}](-). Their structures were confirmed by the data from mass spectrometry, IR, H-1, B-11, and C-13 NMR spectroscopy. The molecular geometry of [2(Z)-B10H9{NH=C(OBu)Me}](-), which formed in nucleophilic addition reaction of n-butyl alcohol to [2-B10H9(Na parts per thousand CMe)](-), was established by X-ray diffraction analysis.
引用
收藏
页码:1694 / 1700
页数:7
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