4.6 Article

A highly selective turn-on fluorescent sensor for zinc ion based on a cinnamyl pyrazoline derivative and its imaging in live cells

Journal

ANALYTICAL METHODS
Volume 10, Issue 16, Pages 1833-1841

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ay00037a

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A fluorescence probe based on cinnamyl pyrazoline was developed and synthesized. The probe detected Zn2+ ion that was mixed with a series of cations in aqueous ethanol with high selectivity and high sensitivity. After adding Zn2+ , the fluorescence intensity was significantly enhanced, with a 56-fold increase. The detection limits and binding constants of 2.95 x 10(-8) M and 1.468 x 10(4) M-1 were calculated by a fluorescence titration experiment. The 1 : 1 binding chemometrics of the 1-Zn2+ complex was analyzed by Job's plot. The probe showed good reversibility when adding PPi. Additionally, the turn-on fluorescent probe with excellent membrane permeability was satisfactorily applied to microscopic imaging for the detection of Zn2+ in baby hamster kidney (BHK)-21 cells.

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