Synthesis of coumarin based fluorescent chemosensors for the detection of metal ions.

The study focused on the synthesis of three coumarin-based chemosensors; hydrazone fluorescent chemosensor , azo-benzothiazole dye and azo-quinoline dye. The hydrazone fluorescent chemosensor was synthesised through multiple reaction steps were the azide functionality at position 8 of the coumarin backbone was replaced with the hydrazone group in the last reaction step. The azo dyes were synthesised through a two step reaction process. The photophysical properties of all three chemosensors were investigated. The hydrazone chemosensor and azo-benzothiazole dye presented high absorption and emission, while the azo-quinoline only presented absorption properties. The chemosensing ability of the three products were investigated through absorption and emission. The hydrazone chemosensor was found to be highly selective towards Fe3+ in water and the dyes were found to be selective towards Hg2+. The mechanisms of interaction between the chemosensors and their selective metal ions were investigated via computational analysis and 1H NMR analysis. All of the chemosensors where characyerised using 1H NMR, Fourier Transform Infrared Spectrometer (FTIR) and the X Ray Chrystal structure for the hydrazone chemosensor was obtained via X ray Chrystallography. Finally, the electron density distribution of the all synthesised compounds their predicted stable metal ion complexes was determined using Density Functionaly Theory (DFT).Thesis (MSc) -- Faculty of Science, School of Biomolecular and Chemical Sciences, 202