Date of Award
8-10-2021
Degree Type
Thesis
Degree Name
Master of Science (MS)
Department
Chemistry
First Advisor
Maged Henary
Abstract
In this study, the synthesis, characterization, optical properties and TD-DFT studies of 21 near infra-red (NIR) fluorophores, and cytotoxicity of selected four compounds are presented. Fluorophores have a chloroacrylic acid acceptor unit and various donor units such as indole, benzothiazole, benzo[e]indole, and quinoline. Further modifications are also done at the linker with t-butyl and phenyl groups. The fluorophores showed strong absorption in the NIR (700-970 nm) region due to their unique intramolecular charge transfer (ICT) between chloroacrylic acid and the donor moieties. The emission wavelength maxima of the fluorophores were between 798-870 nm. Compound 123 with quinoline donor moiety, showed an emission wavelength above 1000 nm. Time dependent density functional theory (TD-DFT) calculations showed that the charge transfer occurs from the donor groups to the acceptor chloroacrylic acid moiety. Fluorophores were also shown to possess a charge separation character.
DOI
https://doi.org/10.57709/23988378
Recommended Citation
Ersoy Ozmen, Guliz, "Synthesis and Optical Properties of Red Shifted Donor Acceptor Fluorophores as Potential Agents for Biomedical Applications." Thesis, Georgia State University, 2021.
doi: https://doi.org/10.57709/23988378
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