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DESIGN AND SYNTHESIS OF TRIAZENE-SUBSTITUTED PUSH-PULL DYES USING FORMAL [2+2] CYCLOADDITION RETROELECTROCYCLIZATION REACTIONS
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Date
2022-1-26
Author
Mammadova, Flora
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Conjugated push-pull chromophores are valuable due to intramolecular electron charge transfer band (ICT), second and third order nonlinear optical properties. These extraordinary features allow to use them in the area of optoelectronics where advanced applications are possible. Organic light emitting diodes (OLEDs), solar cells, organic field effect transistors (OFETs) are some examples. Synthesis of push pull chromophores is possible by click-type [2+2] cycloaddition retroelectrocyclization (CA-RE) reactions. In this thesis, triazene-substituted terminal and non-terminal alkyne substrates are used as electron-donors which react with strong electron-acceptors TCNE and TCNQ. Optoelectronic properties of obtained push-pull dyes are characterized via UV/Vis spectroscopy and theoretical calculations
Subject Keywords
[2+2] cycloaddition-retroelectrocyclization, push-pull chromophores, triazene, optoelectronics
URI
https://hdl.handle.net/11511/96218
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Graduate School of Natural and Applied Sciences, Thesis
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F. Mammadova, “DESIGN AND SYNTHESIS OF TRIAZENE-SUBSTITUTED PUSH-PULL DYES USING FORMAL [2+2] CYCLOADDITION RETROELECTROCYCLIZATION REACTIONS,” M.S. - Master of Science, Middle East Technical University, 2022.
