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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Published in | ChemistryOpen (Weinheim) Vol. 7; no. 8; pp. 639 - 644 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
01.08.2018
|
Online Access | Get full text |
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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. |
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ISSN: | 2191-1363 2191-1363 |
DOI: | 10.1002/open.201800083 |