A new perylenediimide with NH functionality as a colorimetric and fluorescent probe for the selective detection of trivalent Fe3+ and Al3+ ions

被引:21
|
作者
Suganya, Sivalingam [1 ]
Namgoong, Jin Woong [2 ]
Mutyala, Anil Kumar [1 ]
Velmathi, Sivan [3 ]
Kim, Jae Pil [2 ]
Park, Jong S. [1 ]
机构
[1] Pusan Natl Univ, Dept Organ Mat Sci & Engn, Busan 46241, South Korea
[2] Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 08826, South Korea
[3] Natl Inst Technol, Dept Chem, Tiruchirappalli 620015, Tamil Nadu, India
基金
新加坡国家研究基金会;
关键词
Perylenediimide; NH binding unit; Colorimetric sensing; Al3+/Fe3+ ion detection; Fluorescence enhancement; Density functional theory; TURN-ON FLUORESCENT; AQUEOUS-MEDIA; NAKED-EYE; ENERGY-TRANSFER; DUAL DETECTION; SENSOR; CHEMOSENSOR; AL(III); DERIVATIVES; PYROPHOSPHATE;
D O I
10.1016/j.jphotochem.2017.04.036
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the synthesis of a new colorimetric probe RI, in which the perylene tetracarboxylicdiimide fluorophore is connected with an adamantly amine unit through the NH binding site. RI was tested with a variety of metal ions and exhibited a significant colorimetric transition in the presence of Fe3+ and Al3+ ions. No significant changes were observed with other metal ions. Absorption measurements indicated that trivalent metal ions Fe3+/Al3+ bind with RI and generate a stable complex. The presence of Fe3+ and Al3+ ions induces new absorption bands with shoulder peaks at 525 nm and 568 nm. The fluorescence intensity of R1 at 579 nm was significantly increased by the addition of Fe(3+)or Al3+ ions. Furthermore, RI was found to be sensitive towards these metal ions at micromolar concentrations. The stoichiometry of RI :Fe3+/Al3+ complexes were confirmed by ESI-MS analysis, and binding constants were calculated using Benesi-Hildebrand plots. The binding mode of RI with metal ions was proposed based on optimized structure from DFT calculation. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:36 / 41
页数:6
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