Issue 43, 2013
From the journal:

Chemical Communications

Spirolactamized benzothiazole-substituted N,N-diethylrhodol: a new platform to construct ratiometric fluorescent probes†

Hui Wen,a   Qian Huang,a   Xiao-Feng Yang*a  and  Hua Lia  

* Corresponding authors

a Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710069, P.R. China
E-mail: xfyang@nwu.edu.cn
Fax: +86 29-88303798

Abstract

A new rhodol dye 3 with an ESIPT unit has been successfully developed, which can serve as a convenient and universal platform for developing ratiometric sensing systems based on the unique spirocyclic ring-opening process. As a model platform, rhodol 3 hydrazide (4) was prepared and it showed ratiometric response toward Cu2+.

Graphical abstract: Spirolactamized benzothiazole-substituted N,N-diethylrhodol: a new platform to construct ratiometric fluorescent probes

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Article information

DOI
https://doi.org/10.1039/C3CC41343H
Article type
Communication
Submitted
21 Feb 2013
Accepted
07 Apr 2013
First published
08 Apr 2013

Chem. Commun., 2013,49, 4956-4958

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Spirolactamized benzothiazole-substituted N,N-diethylrhodol: a new platform to construct ratiometric fluorescent probes

H. Wen, Q. Huang, X. Yang and H. Li, Chem. Commun., 2013, 49, 4956 DOI: 10.1039/C3CC41343H

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