硅桥双(12-冠-4)醚作为钠离子选择电极的离子载体。

IF 4.6 2区 化学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecules Pub Date : 2025-02-17 DOI:10.3390/molecules30040925
Shoichi Katsuta, Yoshiyasu Ino, Hiroto Wakabayashi
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引用次数: 0

摘要

合成了一种新的Na+离子载体,硅原子上有两个12冠-4基团,硅原子上有疏水烃基团。在室温和氮气气氛下,二氯二有机硅烷与2-羟甲基-12-冠-4简单混合制备了硅桥接的双(12-冠-4)s,产率高。合成了7个不同取代基的化合物。为了研究它们作为离子载体的性能,制备了含有它们的PVC膜型离子选择电极,并测定了它们的离子选择系数。典型的选择性序列为Na+ > K+ > Rb+ > Cs+ > NH4+ > Li+ > Ca2+ > Mg2+ > H+。选择性的大小取决于硅原子上烃类取代基的结构。具有两个2-乙基己基的化合物具有特别好的Na+选择性,并且电极的性能等于或优于使用市售的Na+离子载体丙二酸桥接bis(12-crown-4)的电极。该电极的老化稳定性也优于另一种已知的Na+离子载体,即四乙基4-叔丁基杯[4]芳烃-O,O',O″,O′-四乙酸酯,具有较高的实用性。
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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Silicon-Bridged Bis(12-crown-4) Ethers as Ionophores for Sodium Ion-Selective Electrodes.

A new Na+ ionophore with two 12-crown-4 moieties on silicon atoms and hydrophobic hydrocarbon groups on silicon atoms has been synthesized. The silicon-bridged bis(12-crown-4)s were easily obtained in high yield by simply mixing dichlorodiorganosilane and 2-hydroxymethyl-12-crown-4 under room temperature and nitrogen atmosphere. Seven compounds with different hydrocarbon substituents were synthesized. To investigate their properties as ionophores, PVC membrane-type ion-selective electrodes incorporating them were prepared, and the ion selectivity coefficients were determined. The typical selectivity sequence is Na+ > K+ > Rb+ > Cs+ > NH4+ > Li+ > Ca2+ > Mg2+ > H+. The magnitude of selectivity depends on the structures of hydrocarbon substituents on the silicon atoms. The compound with two 2-ethylhexyl groups has particularly good Na+ selectivity, and the performance of the electrode is equal to or better than that of an electrode using a commercially available Na+ ionophore, malonate-bridged bis(12-crown-4). The electrode also showed better-aging stability than that of another known Na+ ionophore, tetraethyl 4-tert-butylcalix[4]arene-O,O',O″,O‴-tetraacetate, indicating high utility.

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来源期刊
Molecules
Molecules 化学-有机化学
CiteScore
7.40
自引率
8.70%
发文量
7524
审稿时长
1.4 months
期刊介绍: Molecules (ISSN 1420-3049, CODEN: MOLEFW) is an open access journal of synthetic organic chemistry and natural product chemistry. All articles are peer-reviewed and published continously upon acceptance. Molecules is published by MDPI, Basel, Switzerland. Our aim is to encourage chemists to publish as much as possible their experimental detail, particularly synthetic procedures and characterization information. There is no restriction on the length of the experimental section. In addition, availability of compound samples is published and considered as important information. Authors are encouraged to register or deposit their chemical samples through the non-profit international organization Molecular Diversity Preservation International (MDPI). Molecules has been launched in 1996 to preserve and exploit molecular diversity of both, chemical information and chemical substances.
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