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几种杯[4]二酰胺化合物的合成及其对某些离子的络合作用 被引量:2

The Synthesis of A Few p-t-butycalix arene Diamides and Its Complexation with Some Ions
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摘要 通过在杯 [4 ]芳烃下沿进行修饰 ,在叔丁基杯 [4 ]芳烃上加溴乙酸乙酯得 2 5 ,2 7-双乙氧羰基甲氧基 -2 6,2 8-二 -羟基杯 [4 ],然后在碱性条件下水解 ,且酰氯化 ,再依次酰胺化 ,制得目标分子 Va~ Vc.采用分子光谱法 ,测定了这些酰胺对一些离子的络合效应 . The calix arene was modified in the lower rim.At first we get the 25,27-bisethoxycarbhonylmethoxy1-26,28-dihydroxyl-calix arene through adding ethyl bromoacetate to t-buty-calix arene.Then hydrolyzation under basic condition and chloride acylation and acylmidation go on in turns,so at last we synthesize targe molecule V a^V c and by comparison of these host molecule's complex effect to ions.
出处 《武汉大学学报(理学版)》 CAS CSCD 北大核心 2001年第4期393-395,共3页 Journal of Wuhan University:Natural Science Edition
关键词 杯[4]芳烃 二酰胺 络合作用 修饰 二胺酰 酰氯化 酰胺化 calix arene calix arenediamide complexation modification in the lower rim p-t-Buty calix arene diamide
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  • 1[1]Vostle F. Comprehensive Surpramolecular Chemistry Volume 2[M]. New York :Elsevier Science Ltd, 1996.104-145.
  • 2[2]Gutsehe C D,Phawa B,No K H,et al. Calixarenes 4:The Synthesis ,Characterization, and Properties of the Calixarenes from p-tert-butyphenol [J]. J Am Chem Soc,1981,103(13) :3 782.
  • 3[3]Talanov V S,Rartsch R A. Highly Selective Preparation of Conformationally vigid Steveoismeric Calix [4]Arenes With two Carboxymethoxy Groups [J]. J Chem Soc Perkin Trans 1,1999,(14) :1 949-1 956.
  • 4[4]Arnard-Neu F,Barrett G,Corry D, et al. Cation Complexation by Chemically Modified Calixarenes,part 10[J]. J Chem Soc Perkin Trans 2, 1997, (3):575.
  • 5[5]Arnard-Neu F, Schving-weill M J, Ziat K. Selective Alkali and Alkaline Earth Catin Complexation by Calixarene Amides[J]. New J Chem, 1991,15: 33-37.

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