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Issue 48, 2010
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Highly activated Michael acceptor by an intramolecular hydrogen bond as a fluorescence turn-on probe for cyanide

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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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Supplementary files

Article information


Submitted
16 Sep 2010
Accepted
11 Oct 2010
First published
01 Nov 2010

Chem. Commun., 2010,46, 9197-9199
Article type
Communication

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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