Article ID Journal Published Year Pages File Type
5279231 Tetrahedron Letters 2009 5 Pages PDF
Abstract

A series of lower rim 1,3-di-derivatives possessing Schiff's base cores were synthesized using triazole unit as linker moiety by further introducing butyl (L2), one -CH2OH (L3) and two -CH2OH (L4)-containing moieties, respectively, in order to bring additional support for ion binding. Based on fluorescence and absorption spectroscopies it has been shown that Zn2+ could be selectively recognized by the Schiff's base core and not by the triazole core among the ten metal ions studied both in methanol and in aqueous solutions of methanol and acetonitrile, wherein the -CH2OH moieties augment the fluorescence response by providing additional coordinations to the Zn2+. Thus L4 exhibited a fluorescence enhancement of ∼65, ∼48 and ∼25-fold in methanol, aqueous solutions of methanol and acetonitrile, with minimum detection limits of 174, 313 and 320 ppb, respectively. Both the excitation and emission wavelengths fall in visible region.

Graphical abstractA series of lower rim 1,3-di-derivatives possessing Schiff's base cores were synthesized using triazole unit as linker moiety by further introducing butyl (L2), one -CH2OH (L3) and two -CH2OH (L4)-containing moieties respectively, in order to bring additional support for ion binding. Based on fluorescence and absorption spectroscopies it has been shown that Zn2+ could be selectively recognized by the Schiff's base core and not by the triazole core among the ten metal ions studied both in methanol and in aqueous solutions of methanol and acetonitrile, wherein the -CH2OH moieties augment the fluorescence response by providing additional coordinations to the Zn2+. Thus L4 exhibited a fluorescence enhancement of ∼65, ∼48 and ∼25-fold in methanol, aqueous solutions of methanol and acetonitrile, with minimum detection limits of 174, 313 and 320 ppb, respectively. Both the excitation and emission wavelengths fall in visible region.Download full-size image

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Physical Sciences and Engineering Chemistry Organic Chemistry
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