Adegoke Oluwasesan, Nyokong Tebello
Department of Chemistry, Rhodes University, Grahamstown, 6140, South Africa.
J Fluoresc. 2014 Mar;24(2):481-91. doi: 10.1007/s10895-013-1317-4. Epub 2013 Oct 27.
We report on the design and application of fluorescent nanoprobes based on the covalent linking of L-glutathione-capped CdSe@ZnS quantum dots (QDs) to newly synthesized unsymmetrically substituted nickel mercaptosuccinic acid triazatetra-benzcorrole (3) and phthalocyanine (4) complexes. Fluorescence quenching of the QDs occurred on conjugation to complexes 3 or 4. The nanoprobes were selectively screened in the presence of different cations and Hg(2+) showed excellent affinity in "turning ON" the fluorescence of the nanoprobes. Experimental results showed that the sensitivity of QDs-4 towards Hg(2+) was much higher than that of QDs-3 nanoprobe. The mechanism of reaction has been elucidated based on the ability of Hg(2+) to coordinate with the sulphur atom of the Ni complex ring and apparently "turn ON" the fluorescence of the linked QDs.
我们报道了基于L-谷胱甘肽包覆的CdSe@ZnS量子点(QDs)与新合成的不对称取代的巯基琥珀酸镍三氮杂四苯并卟啉(3)和酞菁(4)配合物共价连接的荧光纳米探针的设计与应用。量子点与配合物3或4共轭时发生荧光猝灭。在不同阳离子存在下对纳米探针进行了选择性筛选,Hg(2+)在“开启”纳米探针荧光方面表现出优异的亲和力。实验结果表明,量子点-4对Hg(2+)的灵敏度远高于量子点-3纳米探针。基于Hg(2+)与镍配合物环中硫原子配位的能力以及明显“开启”连接的量子点荧光的能力,阐明了反应机理。