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Fluorescent ZnII Chemosensor Mediated by a 1,8-Naphthyridine Derivative and It's Photophysical Properties.


ABSTRACT: One of the greatest challenges in using fluorescent chemosensors for highly selective and sensitive transition-metal ions is finding an efficient and simple method for its synthesis. In this study, a highly efficient fluorescence chemosensor for ZnII was developed from N-Boc-L-proline modified 1,8-naphthyridine. The fluorescence intensity of the chemosensor was increased significantly only in the presence of ZnII ion which provided a perceived color change for rapid visual sensing, while other metal ions showed fluorescence quenching or little changes. It was worth noting that the chemosensor L distinguished ZnII from CdII commonly having similar properties. The solvent effect and possible bonding mode for fluorescence enhancement have been also discussed. Results of this study indicated that the Boc-group in l-proline significantly improved the sensitivity and selectivity for ZnII detection performance, as confirmed by comparison experiments and time dependent-density functional theory (TD-DFT) calculations.

SUBMITTER: Luo W 

PROVIDER: S-EPMC6104432 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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Fluorescent Zn<sup>II</sup> Chemosensor Mediated by a 1,8-Naphthyridine Derivative and It's Photophysical Properties.

Luo Wenxiu W   Liu Mengjiao M   Yang Ting T   Yang Xia X   Wang Yi Y   Xiang Haifeng H  

ChemistryOpen 20180821 8


One of the greatest challenges in using fluorescent chemosensors for highly selective and sensitive transition-metal ions is finding an efficient and simple method for its synthesis. In this study, a highly efficient fluorescence chemosensor for Zn<sup>II</sup> was developed from <i>N</i>-Boc-<i>L-</i>proline modified 1,8-naphthyridine. The fluorescence intensity of the chemosensor was increased significantly only in the presence of Zn<sup>II</sup> ion which provided a perceived color change for  ...[more]

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