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

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

Research output: Contribution to journalArticle

48 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)4143-4148
Number of pages6
JournalOrganic and Biomolecular Chemistry
Volume13
Issue number14
Early online date4 Dec 2014
DOIs
Publication statusPublished - 14 Apr 2015

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Naphthalimides
Fluorides
fluorides
Boronic Acids
evaluation
probes
synthesis
Amines
esters
Quenching
amines
Esters
Fluorescence
selectivity
quenching
Ions
fluorescence
acids
ions
interactions

Cite this

Synthesis and evaluation of a boronate-tagged 1,8-naphthalimide probe for fluoride recognition. / Xu, Su-Ying; Sun, Xiaolong; Ge, Haobo; Arrowsmith, Rory L.; Fossey, John S.; Pascu, Sofia I.; Jiang, Yun-Bao; James, Tony D.

In: Organic and Biomolecular Chemistry, Vol. 13, No. 14, 14.04.2015, p. 4143-4148.

Research output: Contribution to journalArticle

Xu, Su-Ying ; Sun, Xiaolong ; Ge, Haobo ; Arrowsmith, Rory L. ; Fossey, John S. ; Pascu, Sofia I. ; Jiang, Yun-Bao ; James, Tony D. / Synthesis and evaluation of a boronate-tagged 1,8-naphthalimide probe for fluoride recognition. In: Organic and Biomolecular Chemistry. 2015 ; Vol. 13, No. 14. pp. 4143-4148.
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