Issue 18, 2013

Reaction-based dual signaling of fluoride ions by resorufin sulfonates

Abstract

We developed new reaction-based probes for the dual signaling of fluoride ions. Selective fluoride-assisted deprotection of resorufin nosylate to generate resorufin fluorochrome was used for signaling. Resorufin nosylate exhibited selective colorimetric and fluorogenic signaling of fluoride ions in acetonitrile. The response from sulfide ions was effectively masked by using the TPEN–Cu2+ complex as a source of Cu2+ ions for masking sulfide. Selective optical signaling of fluoride was possible in the presence of commonly encountered anions with a detection limit of 1.9 × 10−6 M.

Graphical abstract: Reaction-based dual signaling of fluoride ions by resorufin sulfonates

Supplementary files

Article information

Article type
Paper
Submitted
09 Jan 2013
Accepted
22 Mar 2013
First published
05 Apr 2013

Org. Biomol. Chem., 2013,11, 2966-2971

Reaction-based dual signaling of fluoride ions by resorufin sulfonates

H. G. Im, H. Y. Kim, M. G. Choi and S. Chang, Org. Biomol. Chem., 2013, 11, 2966 DOI: 10.1039/C3OB00040K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements