Synthesis of a tweezer-like bis(arylthiaalkoxy)calix[4]arene as a cation sensor for ion-selective electrodes: an investigation of the influence of neighboring halogen atoms on cation selectivity‡

Literature Information

Publication Date 2003-02-25
DOI 10.1039/B211381C
Impact Factor 3.876
Authors

Xianshun Zeng, Langxing Chen, Xuebing Leng, Fengbo Xu, Qinshan Li, Xiwen He, Wenqin Zhang, Zheng-Zhi Zhang


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Abstract

Two novel tweezer-like 25,27-dihydroxy-26,28-bis(phenylthiaethoxy)calix[4]arenes 6 and 7 were synthesized by the reaction of 25,27-dihydroxy-26,28-bis(bromoethoxy)calix[4]arenes 3 and 4 for the evaluation of their ion-selectivity in ion-selective electrodes (ISEs). X-ray structural analysis indicated that calix[4]arene 7 is in an interesting infinite linear aggregate via self-inclusion. For investigation of the influences of substitutes on the behavior of the ISEs, the halogen substituted aryl analogues of 25,27-dihydroxy-26,28-bis(arylthiaethoxy)calix[4]arenes 8–12 were also synthesized and their ISE performances were evaluated under the same conditions. ISEs based on 6–12 as neutral ionophores were prepared, and their selectivity coefficients for Ag+ (log KpotAg,M) were investigated against other alkali metal, alkaline-earth metal, lead, ammonium ions and some transition metal ions using the fixed interference method (FIM). These ISEs showed excellent Ag+ selectivity over most of the interfering cations examined, except for Hg2+ having relative smaller interference (log KpotAg,Hg ≤ 2.1). The 19F NMR spectra of 9 and 9·AgClO4 were recorded for investigation the fluorine environments in the complex. The 19F NMR spectra strongly suggested that the fluorine atoms on ionophore 9 participated in ligation with silver cation.

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Front/Back Matter

DOI: 10.1039/C4GC90031F

Inside front cover

Cover

DOI: 10.1039/C4GC90036G

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Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry
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