Issue 4, 2015

Naphthalimide-based fluorescent photoinduced electron transfer sensors for saccharides

Abstract

The design and synthesis of two novel fluorescent sensors based on the photoinduced electron transfer (PET) mechanism for the detection of saccharides in aqueous medium is described. These sensors are based on the 4-amino-1,8-naphthalimide fluorophore, which absorbs and emits at ∼400 nm and ∼530 nm, respectively. By incorporating a phenylboronic acid receptor at the 4-position through a piperazine linker, high sensitivity was achieved for the sensing of saccharides. Both probes showed pH-dependent fluorescence intensities, with pKa values of 4.8 (PET-S1) and 4.4 (PET-S2), respectively. After binding with sugars, up to 50-fold and 5-fold fluorescence enhancements for PET-S1 and PET-S2 were observed at pH 7.4, which allows them to be used under physiological conditions. The switch-on responses of both probes toward saccharides demonstrating the suppression of PET from the amino group to the fluorophore. The probes showed high sensitivity towards D-fructose and D-sorbitol. Probe PET-S1 was used to detect fructose in honey and beverages with good recovery.

Graphical abstract: Naphthalimide-based fluorescent photoinduced electron transfer sensors for saccharides

Supplementary files

Article information

Article type
Paper
Submitted
29 Oct 2014
Accepted
04 Dec 2014
First published
04 Dec 2014

RSC Adv., 2015,5, 2837-2843

Naphthalimide-based fluorescent photoinduced electron transfer sensors for saccharides

S. Liu, H. Bai, Q. Sun, W. Zhang and J. Qian, RSC Adv., 2015, 5, 2837 DOI: 10.1039/C4RA13414A

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