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使用Zr(IV)-卟啉作为中性载体的具有增强氟选择性的聚合物膜电极。

Polymeric membrane electrodes with enhanced fluoride selectivity using Zr(IV)-porphyrins functioning as neutral carriers.

作者信息

Górski Lukasz, Meyerhoff Mark E, Malinowska Elzbieta

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, Warsaw University of Technology, 00-664 Warsaw, Poland.

出版信息

Talanta. 2004 May 10;63(1):101-7. doi: 10.1016/j.talanta.2003.11.022.

Abstract

Poly(vinyl chloride) polymeric membranes plasticized with o-NPOE (o-nitrophenyl octyl ether) or DOS (dibutyl sebacate) and containing Zr(IV)-octaethyl(OEP)- or Zr(IV)-tetraphenylporphyrins (TPP) along with lipophilic cationic additives (tridodecylmethylammonium chloride; TDMACl) are examined potentiometrically and optically with respect to their response toward fluoride. It is shown that these zirconium porphyrins can function as neutral anion carriers within the organic membranes of the electrodes. Spectrophotometric measurements of thin polymeric films indicate that the presence of lipophilic cationic sites in the form of TDMA(+) and use of lower dielectric constant plasticizer (DOS) prevents formation of metalloporphyrin dimers in the organic polymer phase, which have been observed previously in polymeric membranes formulated with the same Zr(IV) porphyrins but with lipophilic anion site additives. By preventing dimer formation, rapid and Nernstian potentiometric response of the corresponding membrane electrodes toward fluoride ion is observed. Indeed, electrodes prepared with PVC/DOS membranes containing Zr(IV)-OEP and 15mol% of TDMACl (relative to the ionophore) exhibit fast (t(95)<15s) and reversible response toward fluoride. The slope of calibration plots are near-Nernstian (-59.9mV per decade). Such electrodes display the following selectivity pattern: ClO(4)(-)>SCN(-)>F(-)>NO(3)(-)>Br(-)>Cl(-), which differs significantly from the classical Hofmeister series, with greatly enhanced potentiometric selectivity toward fluoride. The data presented herein, coupled with results from a previous study, confirm that Zr(IV) porphyrins can serve as either charged or neutral type anion carriers with respect to their enhanced interactions with fluoride when used as ionophores to prepare liquid-polymeric membrane electrodes, and that the nature of membrane additives and plasticizer dictates the response mechanism at play for given membrane formulations.

摘要

研究了用邻硝基苯基辛基醚(o-NPOE)或癸二酸二丁酯(DOS)增塑、含有Zr(IV)-八乙基卟啉(OEP)或Zr(IV)-四苯基卟啉(TPP)以及亲脂性阳离子添加剂(三(十二烷基)甲基氯化铵;TDMACl)的聚氯乙烯(PVC)聚合物膜对氟化物的电位响应和光学响应。结果表明,这些锆卟啉可以在电极的有机膜中作为中性阴离子载体发挥作用。对聚合物薄膜的分光光度测量表明,以TDMA(+)形式存在的亲脂性阳离子位点以及使用较低介电常数的增塑剂(DOS)可防止在有机聚合物相中形成金属卟啉二聚体,而在使用相同Zr(IV)卟啉但添加亲脂性阴离子位点添加剂配制的聚合物膜中曾观察到这种二聚体。通过防止二聚体形成,观察到相应膜电极对氟离子具有快速且能斯特响应。实际上,用含有Zr(IV)-OEP和15mol%TDMACl(相对于离子载体)的PVC/DOS膜制备的电极对氟化物表现出快速(t(95)<15s)且可逆的响应。校准曲线的斜率接近能斯特斜率(每十倍变化-59.9mV)。这类电极呈现出以下选择性模式:ClO(4)(-)>SCN(-)>F(-)>NO(3)(-)>Br(-)>Cl(-),这与经典的霍夫迈斯特序列有显著不同,对氟化物的电位选择性大大增强。本文给出的数据,结合先前一项研究的结果,证实了当用作离子载体来制备液-聚合物膜电极时,Zr(IV)卟啉相对于其与氟化物增强的相互作用可作为带电或中性类型的阴离子载体,并且膜添加剂和增塑剂的性质决定了给定膜配方中起作用的响应机制。

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