Quinoline-based molecular clips for selective fluorescent detection of Zn2
New selective Zn2+ fluorescent sensors, di(2-quinoline-carbaldehyde)-2,2'-bibenzoyl-hydrazone (QB1) and di(2-quinolinecarbaldehyde)-6,6'-dicarboxylic acid hydrazone-2,2'-bipyridine (QB2), have been designed and prepared. Both QB sensors exhibit an emission band centered at 405 nm (exc...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2006-01 (29), p.3528-3533 |
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container_title | Dalton transactions : an international journal of inorganic chemistry |
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creator | Wu, Da-Yu Xie, Li-Xia Zhang, Chang-Li Duan, Chun-Ying Zhao, Yong-Gang Guo, Zi-Jian |
description | New selective Zn2+ fluorescent sensors, di(2-quinoline-carbaldehyde)-2,2'-bibenzoyl-hydrazone (QB1) and di(2-quinolinecarbaldehyde)-6,6'-dicarboxylic acid hydrazone-2,2'-bipyridine (QB2), have been designed and prepared. Both QB sensors exhibit an emission band centered at 405 nm (excitation at 350 nm) with low quantum yield. Zinc binding not only red-shifts the emission band to 500 nm, but also enhances the fluorescence intensity by an order of magnitude based on the deprotonization strategy via self-assembly. These probes are highly selective for Zn2+ over biologically relevant alkali metals, alkaline earth metals and the first row transition metals such as Mn2+, Fe2+, Co2+ and Ni2+ in buffered aqueous DMSO solution. |
doi_str_mv | 10.1039/b605653a |
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Both QB sensors exhibit an emission band centered at 405 nm (excitation at 350 nm) with low quantum yield. Zinc binding not only red-shifts the emission band to 500 nm, but also enhances the fluorescence intensity by an order of magnitude based on the deprotonization strategy via self-assembly. 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Both QB sensors exhibit an emission band centered at 405 nm (excitation at 350 nm) with low quantum yield. Zinc binding not only red-shifts the emission band to 500 nm, but also enhances the fluorescence intensity by an order of magnitude based on the deprotonization strategy via self-assembly. 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Both QB sensors exhibit an emission band centered at 405 nm (excitation at 350 nm) with low quantum yield. Zinc binding not only red-shifts the emission band to 500 nm, but also enhances the fluorescence intensity by an order of magnitude based on the deprotonization strategy via self-assembly. These probes are highly selective for Zn2+ over biologically relevant alkali metals, alkaline earth metals and the first row transition metals such as Mn2+, Fe2+, Co2+ and Ni2+ in buffered aqueous DMSO solution.</abstract><cop>England</cop><pmid>16855754</pmid><doi>10.1039/b605653a</doi><tpages>6</tpages></addata></record> |
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title | Quinoline-based molecular clips for selective fluorescent detection of Zn2 |
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