Phenanthroline complexes bearing fused dipyrrolylquinoxaline anion recognition sites: Efficient fluoride anion receptors.

被引:344
作者
Mizuno, T [1 ]
Wei, WH [1 ]
Eller, LR [1 ]
Sessler, JL [1 ]
机构
[1] Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
关键词
D O I
10.1021/ja017298t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel anion recognition host molecules, tris-1,10-phenanthroline cobalt(III) and bis-2,2-bipyridine mono-1,10-phenanthroline ruthenium(II) complexes bearing fused dipyrrolylquinoxaline moieties have been synthesized. As determined by UV-vis spectroscopic and electrochemical studies, these metal complexes bind fluoride with high affinity in polar media both in absolute terms and relative to the metal-free phenanthroline dipyrrolylquinozaline precursor from which they are derived (fluoride is bound to the tris-1,10-phenanthroline cobalt(III) dipyrrolylquinoxaline system with a 1:1 binding constant of 54000 M-1 in DMSO). The large observed binding constants are ascribed to two factors, (i) the presence of a phenanthroline-coordinated cationic charge that decreases the electron density on the pyrrole NH protons and (ii) pure electrostatic effects. Copyright © 2002 American Chemical Society.
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收藏
页码:1134 / 1135
页数:2
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