Issue 57, 2014

Electrochemical discrimination of phthalic acid among three phthalic acid isomers based on an N-butylaminomethyl-ferrocene derivative

Abstract

A chemosensor compound (1) consisting of a central ferrocene with two butylaminomethyl arms showed unexpected facile electrochemical oxidation of the secondary amines in proximity to the ferrocene, which was utilized for electrochemical discrimination of phthalic acid selectively over two other isomers, isophthalic acid and terephthalic acid.

Graphical abstract: Electrochemical discrimination of phthalic acid among three phthalic acid isomers based on an N-butylaminomethyl-ferrocene derivative

Supplementary files

Article information

Article type
Communication
Submitted
05 Mar 2014
Accepted
27 May 2014
First published
27 May 2014
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2014,50, 7670-7672

Electrochemical discrimination of phthalic acid among three phthalic acid isomers based on an N-butylaminomethyl-ferrocene derivative

J. Yoon, J. R. Jadhav, J. M. Kim, M. Cheong, H. Kim and J. Kim, Chem. Commun., 2014, 50, 7670 DOI: 10.1039/C4CC01659A

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