Issue 48, 2010
From the journal:

Chemical Communications

Highly activated Michael acceptor by an intramolecular hydrogen bond as a fluorescence turn-on probe for cyanide†

Seokan Parka  and  Hae-Jo Kim*a  

* Corresponding authors

a Department of Chemistry, Hankuk University of Foreign Studies, Yongin 449-791, Korea
E-mail: haejkim@hufs.ac.kr
Fax: +82 31-330-4566
Tel: +82 31-330-4703

Abstract

An activated Michael acceptor type of probe by an intramolecular hydrogen bond has shown a selective fluorescence turn-on response to cyanide through a conjugated addition of the nucleophilic anion to the enone probe with a 1300-fold increase in its fluorescence intensity.

Graphical abstract: Highly activated Michael acceptor by an intramolecular hydrogen bond as a fluorescence turn-on probe for cyanide

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Article information

DOI
https://doi.org/10.1039/C0CC03910A
Article type
Communication
Submitted
16 Sep 2010
Accepted
11 Oct 2010
First published
01 Nov 2010

Chem. Commun., 2010,46, 9197-9199

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Highly activated Michael acceptor by an intramolecular hydrogen bond as a fluorescence turn-on probe for cyanide

S. Park and H. Kim, Chem. Commun., 2010, 46, 9197 DOI: 10.1039/C0CC03910A

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