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A novel and fast responsive turn-on fluorescent probe for the highly selective detection of Cd2+ based on photo-induced electron transfer.


ABSTRACT: A novel, highly sensitive and fast responsive turn-on fluorescence probe, 2,2'-((1E,1'E)-((1,10-phenanthroline-2,9-diyl)bis(methanylylidene)) bis(azanylylidene)) diphenol (ADMPA), for Cd2+ was successfully developed based on 2,9-dimethyl-1,10-phenanthroline and o-aminophenol. ADMPA showed a remarkable fluorescence enhancement toward Cd2+ against other competing cations, owing to the suppression of the photo-induced electron transfer (PET) and CH[double bond, length as m-dash]N isomerization. A good linear relationship (R 2 = 0.9960) was obtained between the emission intensity of ADMPA and the concentration of Cd2+ (0.25-2.5 μM) with a detection limit of 29.3 nM, which was much lower than that reported in literature. The binding stoichiometry between ADMPA and Cd2+ was 2 : 1 as confirmed by the Job's Plot method, which was further confirmed by a 1H NMR titration experiment. Moreover, the ADMPA probe was successfully applied to detect Cd2+ in real water samples with a quick response time of only 6.6 s, which was about 3-40 times faster than the reported cadmium ion probe.

SUBMITTER: Huang MX 

PROVIDER: S-EPMC9074931 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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A novel and fast responsive turn-on fluorescent probe for the highly selective detection of Cd<sup>2+</sup> based on photo-induced electron transfer.

Huang Meng-Xia MX   Lv Cai-Hua CH   Huang Qing-Da QD   Lai Jia-Ping JP   Sun Hui H  

RSC advances 20191105 62


A novel, highly sensitive and fast responsive turn-on fluorescence probe, 2,2'-((1<i>E</i>,1'<i>E</i>)-((1,10-phenanthroline-2,9-diyl)bis(methanylylidene)) bis(azanylylidene)) diphenol (ADMPA), for Cd<sup>2+</sup> was successfully developed based on 2,9-dimethyl-1,10-phenanthroline and <i>o</i>-aminophenol. ADMPA showed a remarkable fluorescence enhancement toward Cd<sup>2+</sup> against other competing cations, owing to the suppression of the photo-induced electron transfer (PET) and CH[double  ...[more]

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