Remarkable thallium(I) selectivity for ion sensors based on π-coordination of calix[4]arene neutral carriers

K. Kimura, Kenta Tatsumi, M. Yokoyama, M. Ouchi, M. Mocerino
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引用次数: 39

Abstract

Calix[4]arene derivatives have been applied as neutral carriers for thallium(I)-selective electrodes, taking advantage of their π-coordination. Calix[4]arene derivatives without any t-butyl group at the upper rim, such as calix[4]arene tetra(propyl ether) and tetra(allyl ether), provided the thallium(I)-selective electrodes with high sensitivity and ion selectivity. t-Butylcalix[4]arene derivatives employed here did not afford very good results as for the thallium(I) neutral carrier. 1H-NMR spectroscopy indicated that thallium(I) complexation by the calixarene neutral carriers is made primarily by π-coordination of their skeletal aromatic rings. The ion-selective electrode based on calix[4]arene tetra(propyl ether) was successfully applied to thallium(I) assays in human urine.
基于杯[4]芳烃中性载体π配位的离子传感器具有显著的铊(I)选择性
杯[4]芳烃衍生物利用其π配位的优势,被用作铊(I)选择性电极的中性载体。杯[4]芳烃衍生物,如杯[4]芳烃四(丙醚)和四(烯丙醚),提供具有高灵敏度和离子选择性的铊(I)选择性电极。本文采用的t-丁基杯[4]芳烃衍生物对于铊(I)中性载体的效果不太好。1H-NMR表明,杯芳烃中性载体与铊(I)的络合主要是通过其骨架芳香环的π配位进行的。基于杯[4]芳烃四(丙醚)的离子选择电极成功应用于人尿中铊(I)的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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