Journal
ANALYTICA CHIMICA ACTA
Volume 632, Issue 1, Pages 9-14Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2007.08.025
Keywords
Rhodamine B hydroxylamide; Fluorescence probe; Cu2+; Cleavable active bond; Fluorescence enhancement
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Rhodamine B hydroxylamide (1) is characterized as a highly selective and sensitive fluorescence probe for Cu2+. Under the optimized conditions, the probe exhibits specific absorbance-on and fluorescence-on responses to Cu2+ only. This remarkable property may allow Cu2+ to be detected directly in the presence of the other transition metal ions, and such an application has been demonstrated to human serum. The reaction mechanism is also investigated and proposed as that the hydroxylamide group of 1 binds Cu2+, and the subsequent complexation of Cu2+ displays a high catalytic activity for the hydrolytic cleavage of the amide bond, causing the release of fluorophore (rhodamine B) and thereby the retrievement of absorbance and fluorescence. The recovered fluorescence intensity is proportional to the concentration of Cu2+ in the range 1-20 mu M. The detection lit-nit for Cu2+ is 33 nM (k = 3). The reaction mechanism described here may be useful for developing excellent spectroscopic probes with cleavable active bonds for other analytes. (C) 2007 Elsevier B.V. All rights reserved.
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