Voltammetric characterization of selective potassium ion transfer across micro-water/1,2-dichloroethane interface facilitated by a novel calix[4]arene derivative
dc.contributor.author | Durmaz, Müge | |
dc.contributor.author | Zor, Erhan | |
dc.contributor.author | Kocabaş, Erdal | |
dc.contributor.author | Bingöl, Haluk | |
dc.contributor.author | Akgemci, Emine Güler | |
dc.date.accessioned | 2020-03-26T18:17:33Z | |
dc.date.available | 2020-03-26T18:17:33Z | |
dc.date.issued | 2011 | |
dc.department | Selçuk Üniversitesi | en_US |
dc.description.abstract | In this study, transfer reactions of alkali and alkaline-earth metal ions across a micro-water/1,2-dichloroethane (1,2-DCE) interface facilitated by a novel calix[4]arene derivative, 5,11,17,23-tetra-tert-butyl-25,27-bis(2'amino-methylpyridine)-26,28-dihydroxy calix[4]arene (APHC4), were investigated by cyclic and differential pulse voltammetry techniques. Well-defined voltammetric behavior was obtained only for K(+) ion among the used metal ions. The electrochemical data were used to determine the stoichiometry and the appropriate association constant of the occurring complex between K(+) ion and APHC4. The obtained steady-state voltammograms indicated that the facilitated transfer process occurs with a TIC/TID mechanism according to 1:1 stoichiometry. The logarithm of the association constant (log beta(0)(1)) of K(APHC4)(+) complex in the DCE phase was calculated to be 6.32. Also, the availability of the facilitated transfer for the design of an amperometric screening sensor for K(+) ion was evaluated in the range of 50-500 mu mol dm(-3). (C) 2011 Elsevier Ltd. All rights reserved. | en_US |
dc.description.sponsorship | TUBITAK (Scientific and Technical Research Council of Turkey)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [TBAG-107T754] | en_US |
dc.description.sponsorship | This work was supported by TUBITAK (Scientific and Technical Research Council of Turkey) under Contract TBAG-107T754. | en_US |
dc.identifier.doi | 10.1016/j.electacta.2011.04.003 | en_US |
dc.identifier.endpage | 5321 | en_US |
dc.identifier.issn | 0013-4686 | en_US |
dc.identifier.issue | 15 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 5316 | en_US |
dc.identifier.uri | https://dx.doi.org/10.1016/j.electacta.2011.04.003 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12395/27046 | |
dc.identifier.volume | 56 | en_US |
dc.identifier.wos | WOS:000292427900004 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | en_US |
dc.relation.ispartof | ELECTROCHIMICA ACTA | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.selcuk | 20240510_oaig | en_US |
dc.subject | Micro-ITIES | en_US |
dc.subject | Ion transfer | en_US |
dc.subject | Potassium ion | en_US |
dc.subject | Amperometric sensor | en_US |
dc.subject | Calix[4]arene | en_US |
dc.title | Voltammetric characterization of selective potassium ion transfer across micro-water/1,2-dichloroethane interface facilitated by a novel calix[4]arene derivative | en_US |
dc.type | Article | en_US |