2015
DOI: 10.1002/bio.3063
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Two new reversible naphthalimide‐based fluorescent chemosensors for Hg2+

Abstract: Naphthalimide-based fluorescent probes 1 and 2 were synthesized, and were designed to form probe-Hg complexes through Hg(2+) ions coordinated to the amide group and imidazole group. They showed high sensitivity and were selective 'naked-eye' chemosensors for Hg(2+) in phosphate buffer. The fluorescence of compounds 1 and 2 could be quenched up to 90% by the addition of Hg(2+) . Reversible probes can detect Hg(2+) ions over a wide pH range (7.0-10.0). Copyright © 2015 John Wiley & Sons, Ltd.

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Cited by 21 publications
(9 citation statements)
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References 29 publications
(30 reference statements)
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“…Two naphthalimide-appended fluorescent probes, Hg-2 and Hg-3 ( Fig. 4), were devised and reported by Li and his research group members (Li et al 2016). In phosphate buffer, the two compounds display ultra-high-level sensitivities and selectivities for Hg 2+ detection.…”
Section: Small-molecule Hg 2+ Probes Based On Naphthalimide Fluorophorementioning
confidence: 99%
See 1 more Smart Citation
“…Two naphthalimide-appended fluorescent probes, Hg-2 and Hg-3 ( Fig. 4), were devised and reported by Li and his research group members (Li et al 2016). In phosphate buffer, the two compounds display ultra-high-level sensitivities and selectivities for Hg 2+ detection.…”
Section: Small-molecule Hg 2+ Probes Based On Naphthalimide Fluorophorementioning
confidence: 99%
“…Structures of ProbesHg-1, Hg-2, and Hg-3(La et al 2016;Li et al 2016) Proton NMR of Probe Hg-1 in the absence and presence of excess Hg 2+ . Key finding: there was an upfield shift in the aromatic protons owing to increased electron density upon protonation(La et al 2016) Scheme of fluorescent Probe Hg-4 exhibiting the PET mechanism(Vonlanthen et al 2014) …”
mentioning
confidence: 99%
“…1,8‐Naphthalimide derivatives have aroused attention when constructing the fluorophore moieties of sensors because of their appealing features of high photostability and quantum yield, they also have strong absorption band in the visible region and large Stokes’ shifts . Accordingly, there has been many applications of 1,8‐naphthalimide derivatives as components of liquid crystal displays, laser active medium, fluorescent markers in biology, photoinduced electron transfer chemosensors, electroluminescence devices and fluorescence switchers and probes .…”
Section: Introductionmentioning
confidence: 99%
“…Sun et al developed a ratiometric fluorescent hydrazine probe 5 (Figure ) by incorporating an acetate moiety onto naphthalimide, a widely used scaffold for the construction of fluorescent probes . Probe 5 displayed a fluorescence maximum at 432 nm.…”
Section: Probes Based On Acetyl Moietymentioning
confidence: 99%