A STUDY OF NEW BIS(MACROCYCLIC POLYAMINE) LIGANDS AS INORGANIC AND ORGANIC ANION RECEPTORS

被引:95
作者
KIMURA, E
KURAMOTO, Y
KOIKE, T
FUJIOKA, H
KODAMA, M
机构
[1] HIROSHIMA UNIV,SCH MED,DEPT MED CHEM,HIROSHIMA 734,JAPAN
[2] FUKUYAMA UNIV,FAC PHARM,FUKUYAMA 72902,JAPAN
[3] HIROSAKI UNIV,COLL GEN EDUC,DEPT CHEM,HIROSAKI,AOMORI 036,JAPAN
关键词
D O I
10.1021/jo00288a009
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Propylene-bridged bisdioxo[16]aneN5(4b) and diether-bridged (5a) and propylene-bridged (5b) bis[16]aneN5ligands [bis(macrocyclic pentaamine)] were synthesized as host molecules for inorganic and organic anion guests. By the polarographic and potentiometric methods, 4b (di- and tetraprotonated) and 5a and 5b (tetra- and hexaprotonated) were found to yield stable 1:1 complexes with citrate3-, AMP2-, ATP4-, HP042-, [Fe(CN)6]4_, and [Fe(CN)6]3- anions. Comparison of these association constants (K) with those of the parent monomeric polyamines reveals that the attachment of the second polyamine moiety always enhances anion encapsulating abilities, suggesting the formation of sandwich-type complexes. Diprotonated tetraoxo[24]aneN86, [6•(H+)2]2+, forms more stable 1:1 complexes with nucleotide anions than the diprotonated 4b, [4b-(H+)2]2+. © 1990, American Chemical Society. All rights reserved.
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页码:42 / 46
页数:5
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