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Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes

The electrochemical properties of diazophenylcalix[4]arenes bearing ortho-carboxyl group (o-CAC) and ortho-ester group (o-EAC), respectively, in the presence of various metal ions were investigated by voltammetry in CH(3)CN. o-CAC and o-EAC showed voltammetric changes toward divalent metal ions and...

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Autores principales: Kim, Bongsu, Kim, Tae Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346698/
https://www.ncbi.nlm.nih.gov/pubmed/25785231
http://dx.doi.org/10.1155/2015/579463
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author Kim, Bongsu
Kim, Tae Hyun
author_facet Kim, Bongsu
Kim, Tae Hyun
author_sort Kim, Bongsu
collection PubMed
description The electrochemical properties of diazophenylcalix[4]arenes bearing ortho-carboxyl group (o-CAC) and ortho-ester group (o-EAC), respectively, in the presence of various metal ions were investigated by voltammetry in CH(3)CN. o-CAC and o-EAC showed voltammetric changes toward divalent metal ions and no significant changes with monovalent alkali metal ions. However, o-CAC preferentially binds with alkaline earth and transition metal ions, whereas no significant changes in voltammetric signals are observed in o-EAC with alkaline earth metal ions. o-EAC only binds with other transition metal ions. This can be explained on metal ion complexation-induced release of proton from the azophenol to the quinone-hydrazone tautomer followed by internal complexation of the metal ion with aid of nitrogen atoms and ortho-carbonyl groups in the diazophenylazocalix[4]arenes.
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spelling pubmed-43466982015-03-17 Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes Kim, Bongsu Kim, Tae Hyun J Anal Methods Chem Research Article The electrochemical properties of diazophenylcalix[4]arenes bearing ortho-carboxyl group (o-CAC) and ortho-ester group (o-EAC), respectively, in the presence of various metal ions were investigated by voltammetry in CH(3)CN. o-CAC and o-EAC showed voltammetric changes toward divalent metal ions and no significant changes with monovalent alkali metal ions. However, o-CAC preferentially binds with alkaline earth and transition metal ions, whereas no significant changes in voltammetric signals are observed in o-EAC with alkaline earth metal ions. o-EAC only binds with other transition metal ions. This can be explained on metal ion complexation-induced release of proton from the azophenol to the quinone-hydrazone tautomer followed by internal complexation of the metal ion with aid of nitrogen atoms and ortho-carbonyl groups in the diazophenylazocalix[4]arenes. Hindawi Publishing Corporation 2015 2015-02-17 /pmc/articles/PMC4346698/ /pubmed/25785231 http://dx.doi.org/10.1155/2015/579463 Text en Copyright © 2015 B. Kim and T. H. Kim. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kim, Bongsu
Kim, Tae Hyun
Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes
title Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes
title_full Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes
title_fullStr Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes
title_full_unstemmed Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes
title_short Electrochemical Studies for Cation Recognition with Diazo-Coupled Calix[4]arenes
title_sort electrochemical studies for cation recognition with diazo-coupled calix[4]arenes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346698/
https://www.ncbi.nlm.nih.gov/pubmed/25785231
http://dx.doi.org/10.1155/2015/579463
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