A naphthalimide-based fluorescent sensor for halogenated solvents

A fluorescent sensor for halogenated solvents termed AMN is reported. AMN shows strong fluorescence in most halogenated solvents (QE > 0.1) but weak fluorescence (QE

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2016-01, Vol.52 (1), p.295-298
Hauptverfasser: Dai, Li, Wu, Di, Qiao, Qinglong, Yin, Wenting, Yin, Jun, Xu, Zhaochao
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container_title Chemical communications (Cambridge, England)
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creator Dai, Li
Wu, Di
Qiao, Qinglong
Yin, Wenting
Yin, Jun
Xu, Zhaochao
description A fluorescent sensor for halogenated solvents termed AMN is reported. AMN shows strong fluorescence in most halogenated solvents (QE > 0.1) but weak fluorescence (QE
doi_str_mv 10.1039/c5cc09403h
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AMN shows strong fluorescence in most halogenated solvents (QE &gt; 0.1) but weak fluorescence (QE&lt;0.01) in most non-halogenated solvents. In chlorinated solvents, the fluorescence intensity decreased with the reduction of chlorine content. On the contrary, in brominated solvents the fluorescence intensity increased with the reduction of bromine content. It is worth mentioning that AMN displayed fluorescence emission centered at 520 nm in CCl 4 with a quantum yield of 0.607, at 556 nm in CHCl 3 with a quantum yield of 0.318, at 584 nm in CH 2 Cl 2 with a quantum yield of 0.128, whereas in CHBr 3 was centered at 441 nm with a quantum yield of 0.012. AMN was shown to have the ability to differentiate CCl 4 , CHCl 3 , CH 2 Cl 2 and CHBr 3 halogenated solvents. 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AMN shows strong fluorescence in most halogenated solvents (QE &gt; 0.1) but weak fluorescence (QE&lt;0.01) in most non-halogenated solvents. In chlorinated solvents, the fluorescence intensity decreased with the reduction of chlorine content. On the contrary, in brominated solvents the fluorescence intensity increased with the reduction of bromine content. It is worth mentioning that AMN displayed fluorescence emission centered at 520 nm in CCl 4 with a quantum yield of 0.607, at 556 nm in CHCl 3 with a quantum yield of 0.318, at 584 nm in CH 2 Cl 2 with a quantum yield of 0.128, whereas in CHBr 3 was centered at 441 nm with a quantum yield of 0.012. AMN was shown to have the ability to differentiate CCl 4 , CHCl 3 , CH 2 Cl 2 and CHBr 3 halogenated solvents. 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AMN shows strong fluorescence in most halogenated solvents (QE &gt; 0.1) but weak fluorescence (QE&lt;0.01) in most non-halogenated solvents. In chlorinated solvents, the fluorescence intensity decreased with the reduction of chlorine content. On the contrary, in brominated solvents the fluorescence intensity increased with the reduction of bromine content. It is worth mentioning that AMN displayed fluorescence emission centered at 520 nm in CCl 4 with a quantum yield of 0.607, at 556 nm in CHCl 3 with a quantum yield of 0.318, at 584 nm in CH 2 Cl 2 with a quantum yield of 0.128, whereas in CHBr 3 was centered at 441 nm with a quantum yield of 0.012. AMN was shown to have the ability to differentiate CCl 4 , CHCl 3 , CH 2 Cl 2 and CHBr 3 halogenated solvents. AMN is the first sensor to have the ability to differentiate CCl 4 , CHCl 3 , CH 2 Cl 2 and CHBr 3 from halogenated solvents.</abstract><cop>England</cop><pmid>26691881</pmid><doi>10.1039/c5cc09403h</doi><tpages>4</tpages></addata></record>
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Carbon tetrachloride
Chlorine
Emission
Fluorescence
Halogenated
Reduction
Sensors
Solvents
title A naphthalimide-based fluorescent sensor for halogenated solvents
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