Synthesis, structure, and complexation properties of tetraamide derivatives of thiacalix[4]arene in different conformations

被引:21
作者
Solovieva, SE
Grüner, M
Omran, AO
Gubaidullin, AT
Litvinov, IA
Habicher, WD
Antipin, IS
Konovalov, AI
机构
[1] Russian Acad Sci, Kazan Res Ctr, AE Arbuzov Organ & Phys Chem Inst, Kazan 420088, Russia
[2] Tech Univ Dresden, Inst Organ Chem, D-01062 Dresden, Germany
[3] Kazan VI Lenin State Univ, Kazan 420008, Russia
基金
俄罗斯基础研究基金会;
关键词
thiacalix[4]arenes; amides; template effect; stereoisomerism; extraction; alkali metals; inclusion compounds; X-ray diffraction analysis; NMR spectroscopy;
D O I
10.1007/s11172-006-0084-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interaction of p-tert-butylthiacalix[4]arene with N,N-diethylchloroacetamide was studied in the presence of alkali metal carbonates in acetone. Three stereoisomers, viz., cone, partial cone, and 1,3-alternate, of the tetraamide derivative of thiacalixarene substituted at the lower rim were synthesized selectively using the template effect of alkali metal cations, as well as a complex of the 1,3-alternate stereoisomer with potassium chloride. The structures of the compounds synthesized were studied by 2D NMR spectroscopy. A high extraction ability of the compounds toward alkali metal cations was demonstrated.
引用
收藏
页码:2104 / 2112
页数:9
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