Issue 7, 2016

Signaling preferences of substituted pyrrole coupled six-membered rhodamine spirocyclic probes for Hg2+ ion detection

Abstract

Two six-membered spirocyclic rhodamine derivatives containing substituted pyrroles (1 and 2) were shown to exhibit preferential dual mode ‘turn-on’ signaling responses in the presence of Hg2+ ions through complexation mediated spiro-ring opening. Although the rate of spiro-ring opening mediated through complexation is much slower in these probes in comparison to their five membered analogues, they exhibited a comparable sensitivity in metal ion detection.

Graphical abstract: Signaling preferences of substituted pyrrole coupled six-membered rhodamine spirocyclic probes for Hg2+ ion detection

Supplementary files

Article information

Article type
Paper
Submitted
18 Dec 2015
Accepted
07 Jan 2016
First published
07 Jan 2016

Org. Biomol. Chem., 2016,14, 2241-2248

Signaling preferences of substituted pyrrole coupled six-membered rhodamine spirocyclic probes for Hg2+ ion detection

B. Biswal, D. Mallick and B. Bag, Org. Biomol. Chem., 2016, 14, 2241 DOI: 10.1039/C5OB02606G

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