Unsymmetrically Substituted Nickel Triazatetra-Benzcorrole and Phthalocynanine Complexes: Conjugation to Quantum Dots and Applications as Fluorescent "Turn ON" Sensors

被引:11
作者
Adegoke, Oluwasesan [1 ]
Nyokong, Tebello [1 ]
机构
[1] Rhodes Univ, Dept Chem, ZA-6140 Grahamstown, South Africa
基金
新加坡国家研究基金会;
关键词
Phthalocyanine; Triazatetra-benzcorrole; Fluorescence enhancement; Quantum dots; Mercury; TETRAAMINO-PHTHALOCYANINE CHARACTERIZATION; METAL-IONS; CDTE; CDSE; NANOCRYSTALS; AGGREGATION; RECOGNITION; PROBE;
D O I
10.1007/s10895-013-1317-4
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
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 Hg2+ showed excellent affinity in "turning ON" the fluorescence of the nanoprobes. Experimental results showed that the sensitivity of QDs-4 towards Hg2+ was much higher than that of QDs-3 nanoprobe. The mechanism of reaction has been elucidated based on the ability of Hg2+ to coordinate with the sulphur atom of the Ni complex ring and apparently "turn ON" the fluorescence of the linked QDs.
引用
收藏
页码:481 / 491
页数:11
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