Colourimetric and fluorimetric metal ion chemosensor based on a benzimidazole functionalised Schiff base

被引:10
作者
Horak, Ema [1 ]
Vianello, Robert [2 ]
Hranjec, Marijana [3 ]
Steinberg, Ivana Murkovic [1 ]
机构
[1] Univ Zagreb, Fac Chem Engn & Technol, Dept Gen & Inorgan Chem, Zagreb, Croatia
[2] Rudjer Boskovic Inst, Computat Organ Chem & Biochem Grp, Zagreb, Croatia
[3] Univ Zagreb, Fac Chem Engn & Technol, Dept Organ Chem, Zagreb, Croatia
关键词
Chemosensor; fluorescence and colourimetric sensor; benzimidazole; Schiff base; AGGREGATION-INDUCED EMISSION; ON FLUORESCENT CHEMOSENSOR; TURN-ON; SUBSTITUTED BENZIMIDAZOLE; PROTONATION EQUILIBRIA; RELAY RECOGNITION; ORGANIC-DYES; LIVING-CELL; MILD-STEEL; GAS-PHASE;
D O I
10.1080/10610278.2018.1436708
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein we present the interaction of benzimidazole based Schiff base 1 with different metal ions studied by absorption and fluorescence spectroscopies and computational modelling. Compound 1 exhibits changes in spectroscopic properties upon chelation with specific metal ions. Its strong absorption band at 425nm is significantly red shifted (=30nm) only upon the complexation with Al3+, an effect observable by a naked eye as a colour change from light- to dark-yellow. Of the metal ions investigated, only Al3+ caused any increase in the fluorescence intensity of 1. All other metal ions, including K(I), Na(I), Ag(I), Li(I), Zn(II), Co(II) and Hg(II), showed a negligible fluorescence response, while Cu(II) and Fe(III) significantly decreased the fluorescence intensity. Therefore, system 1 is a promising colourimetric sensor for Al3+, and a fluorescence sensor for Cu2+ and Fe3+ ions. Computational analysis revealed that 1 is unionized in ethanol solution, while it becomes di-deprotonated to 1 (2-) upon the complexation with Al3+. This changes the electronic structure of 1 and leaves no acidic hydrogen atoms to allow the ESIPT process. On the other hand, the presence of monovalent metal cations induces only mono-deprotonation to 1 (-) , which turns out to be an insufficient electronic change to be spotted in the recorded spectra. [GRAPHICS] .
引用
收藏
页码:891 / 900
页数:10
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