Issue 14, 2015
From the journal:

Organic & Biomolecular Chemistry

Synthesis and evaluation of a boronate-tagged 1,8-naphthalimide probe for fluoride recognition†

Su-Ying Xu,a   Xiaolong Sun,a   Haobo Ge,a   Rory L. Arrowsmith,a   John S. Fossey,b   Sofia I. Pascu,*a   Yun-Bao Jiang*c  and  Tony D. James*a  

* Corresponding authors

a Department of Chemistry, University of Bath, Bath BA2 7AY, UK
E-mail: t.d.james@bath.ac.uk, s.pascu@bath.ac.uk

b School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, UK

c Department of Chemistry, College of Chemistry and Chemical Engineering, and the MOE Key Laboratory of Analytical Sciences, Xiamen University, Xiamen 361005, China
E-mail: ybjiang@xmu.edu.cn

Abstract

A biocompatible fluoride receptor has been developed where the interaction between the boronic acid ester and amine (NH) results in fluoride ion selectivity and enhanced fluorescence quenching.

Graphical abstract: Synthesis and evaluation of a boronate-tagged 1,8-naphthalimide probe for fluoride recognition

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Article information

DOI
https://doi.org/10.1039/C4OB02267J
Article type
Communication
Submitted
27 Oct 2014
Accepted
04 Dec 2014
First published
04 Dec 2014
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2015,13, 4143-4148

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Synthesis and evaluation of a boronate-tagged 1,8-naphthalimide probe for fluoride recognition

S. Xu, X. Sun, H. Ge, R. L. Arrowsmith, J. S. Fossey, S. I. Pascu, Y. Jiang and T. D. James, Org. Biomol. Chem., 2015, 13, 4143 DOI: 10.1039/C4OB02267J

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