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Spectrochim Acta A Mol Biomol Spectrosc ; 300: 122832, 2023 Nov 05.
Artículo en Inglés | MEDLINE | ID: mdl-37290242

RESUMEN

Fluorene-based low molar weight derivatives were synthesized in Suzuki reactions by using key starting materials 9-benzylidene-2,7-dibromofluorene or 3-(2,7-dibromofluoren-9-ylmethylen)-9-ethylcarbazole and various aryl boronic acids. Photophysical properties of the compounds were investigated in different solutions as well as in solid state. The thermal investigations showed that the obtained compounds are highly thermally stable with temperatures of 5% mass loss (T5%) in the range of 311-432 °C. Some of the compounds also exhibited very high glass transition temperatures exceeding 125 °C. The presented molecules were electrochemically active and showed the energy band gap below 2.97 eV. The investigations were supported by DFT calculations and the photovoltaic ability of the presented compounds was tested in the organic-inorganic solar cells.


Asunto(s)
Ácidos Borónicos , Fluorenos , Teoría Funcional de la Densidad , Modelos Teóricos
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