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Synthesis of triazene and aniline-substituted nlophores via click-type transformations and investigation of their linear/nonlinear optical properties
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Fevzi Can İnyurt Tez1.pdf
Date
2024-7
Author
İnyurt, Fevzi Can
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Push-pull chromophores have been studied extensively and gained importance throughout the years due to their significant characteristics, such as strong intramolecular charge transfer bands and high second- and third-order optical nonlinearities. These properties make them suitable for application in several areas of optoelectronics, such as organic light-emitting diodes (OLEDs), solar cells, organic field effect transistors (OFETs), and non-linear optical (NLO) devices. Synthesis of D-A-D type chromophores can be achieved by click-type thermal [2+2] cycloaddition and [2+2] cycloaddition-retroelectrocyclization reactions. Dialkylated triazene and aniline-substituted alkynes will be synthesized as the first aim of the thesis. Then, thermal [2+2] cycloaddition and [2+2] cycloaddition-retroelectrocyclization reactions of alkynes with a strong electron acceptors DDQ, TCNE, and TCNQ will be investigated to access target NLOphores. Optoelectronic properties of the target chromophoric structures will be further examined via UV/Vis spectroscopy and computational studies.
Subject Keywords
Triazene
,
Chromophores
,
NLOphores
,
Diethylaniline
URI
https://hdl.handle.net/11511/110388
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Graduate School of Natural and Applied Sciences, Thesis
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F. C. İnyurt, “Synthesis of triazene and aniline-substituted nlophores via click-type transformations and investigation of their linear/nonlinear optical properties,” M.S. - Master of Science, Middle East Technical University, 2024.