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New Method for Synthesis of Substituted 1-Amidine-closo-decaborates [1-B10H9NH=C(R1)NHR2] (R1 = Me, iPr, Ph; R2 = nBu, Bn)
Russian Journal of Inorganic Chemistry ( IF 2.1 ) Pub Date : 2023-12-15 , DOI: 10.1134/s0036023623601733
A. A. Bil’bulyan , A. V. Nelyubin , N. A. Selivanov , A. Yu. Bykov , I. N. Klyukin , A. P. Zhdanov , K. Yu. Zhizhin , N. T. Kuznetsov

Abstract

The process of nucleophilic substitution of the phenyliodonium substituent in the [1-B10H9IPh] anion with primary amines in organic nitriles has been studied. It has been shown that the reaction proceeds with the formation of a mixture of products, namely, 1-monoalkylammonio-closo-decaborate and the corresponding amidine, which is formed when an amine molecule is added to the nitrile. The resulting products have been characterized by 1H, 11B, 13C NMR spectroscopies, IR absorption spectroscopy, and high-resolution ESI mass spectroscopy.



中文翻译:


取代 1-脒-近十硼酸盐 [1-B10H9NH=C(R1)NHR2](R1 = Me、iPr、Ph;R2 = nBu、Bn)的合成新方法


 抽象的


研究了[1-B 10 H 9 IPh] 阴离子中的苯基碘取代基与有机腈中伯胺的亲核取代过程。已经表明,该反应随着产物混合物的形成而进行,即1-单烷基铵-近十硼酸盐和相应的脒,其是在将胺分子添加到腈时形成的。所得产物通过 1 H、 11 B、 13 C NMR光谱、IR吸收光谱和高分辨率ESI质谱进行表征。

更新日期:2023-12-16
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