Synthesis of amino-containing meso-aryl-substituted porphyrins and their conjugates with the closo-decaborate anion

被引：0

作者：

K. A. Zhdanova

A. P. Zhdanov

A. V. Ezhov

N. A. Bragina

K. Yu. Zhizhin

I. P. Ushakova

A. F. Mironov

N. T. Kuznetsov

机构：

[1] M. V. Lomonosov Moscow State University of Fine Chemical Technologies,N. S. Kurnakov Institute of General and Inorganic Chemistry

[2] Russian Academy of Sciences,undefined

来源：

Russian Chemical Bulletin | 2014年 / 63卷

关键词：

macrocyclic compounds; -aryl-substituted porphyrins; aminoporphyrins; -decaborate anion; addition to nitrogen-carbon multiple bonds;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Amphiphilic meso-aryl-substituted porphyrins containing an amino group and long-chain hydrophobic substituents were synthesized. Two strategies of the synthesis of asymmetric amino-containing porphyrins using p-acetamidobenzaldehyde and p-nitrobenzaldehyde were developed and investigated. A series of new substituted porphyrin-containing closo-decaborates were prepared based on the synthesized porphyrins and nitrilium derivatives of the closo-decaborate anion [B10H10]2−.

引用

页码：194 / 200

页数：6

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