Fluorescent Zn II 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 Zn II was developed from N ‐Boc‐ L‐ proline m...

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Bibliographic Details
Published inChemistryOpen (Weinheim) Vol. 7; no. 8; pp. 639 - 644
Main Authors Luo, Wenxiu, Liu, Mengjiao, Yang, Ting, Yang, Xia, Wang, Yi, Xiang, Haifeng
Format Journal Article
LanguageEnglish
Published 01.08.2018
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Summary: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 Zn II 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 Zn II 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 Zn II from Cd II 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 Zn II detection performance, as confirmed by comparison experiments and time dependent‐density functional theory (TD‐DFT) calculations.
ISSN:2191-1363
2191-1363
DOI:10.1002/open.201800083