Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on 1,3-dipolar cycloaddition

被引:8
|
作者
Burilov, V. A. [1 ]
Epifanova, N. A. [2 ]
Popova, E. V. [2 ]
Vasilevsky, S. F. [3 ]
Solovieva, S. E. [2 ]
Antipin, I. S. [1 ,2 ]
Konovalov, A. I. [1 ,2 ]
机构
[1] Kazan Volga Reg Fed Univ, Kazan 420008, Russia
[2] Russian Acad Sci, Kazan Sci Ctr, AE Arbuzov Organ & Phys Chem Inst, Kazan 420088, Russia
[3] Russian Acad Sci, Inst Chem Kinet & Combust, Siberian Branch, Novosibirsk 630090, Russia
基金
俄罗斯基础研究基金会;
关键词
calix[4] arenes; benzyl azides; 1,3-dipolar cycloaddition; 1,2,3-triazoles; fluorescence; STRUCTURAL-CHARACTERIZATION; MOLECULAR TECTONICS; COORDINATION; COMPLEXES; TRIAZOLES; LIGANDS; AZIDES;
D O I
10.1007/s11172-013-0104-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Regioselective synthesis of 1,2,3-triazolyl derivatives of calix[4]arenes based on the 1,3-dipolar cycloaddition of substituted benzyl azides to tetra(propargyloxy)calix[4]arenes in the presence of copper iodide was carried out. The presence of the p-methoxybenzyl substituent in the triazole ring leads to a dramatic (more than tenfold) increase in the fluorescence of the corresponding macrocycle in a region of 290-310 nm.
引用
收藏
页码:767 / 772
页数:6
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