Synthesis, photophysical properties and DFT analysis of highly substituted pyrido carbazole-based “push pull” chromophores
نویسندگان
چکیده
منابع مشابه
Photophysical properties of photoactive molecules with conjugated push-pull structures.
The photophysical properties of two newly synthesized photoactive compounds with asymmetrical D-pi-A structure and symmetrical D-pi-A-pi-D structure are investigated in different aprotic solvents by steady-state and femtosecond fluorescence depletion measurements. It is found that the asymmetrical DA compound has larger dipole moment change than that of the symmetrical DAD compound upon excitat...
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Synthesis, Characterization and Photophysical Properties of Pyridine-Carbazole Acrylonitrile Derivatives
We synthesized three novel highly fluorescent compounds, 2-(2'-pyridyl)-3-(N-ethyl-(3'-carbazolyl))acrylonitrile, 2-(3"-pyridyl)-3-(N-ethyl-(3'-carbazolyl))acrylonitrile, and 2-(4-pyridyl)-3-(N-ethyl-(3'-carbazolyl))acrylonitrile by Knoevenagel condensation. The first two were synthesized without solvent in the presence of piperidine as a catalyst; the third was synthesized without a catalyst a...
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The structure-property characteristics of a series of newly synthesized intramolecular chargetransfer (ICT) compounds, single-branch monomer with triphenylmethane as electron donor and 2,1,3-benzothiadiazole as acceptor, the corresponding two-branch dimer and threebranch trimer, have been investigated by means of steady-state and femtosecond timeresolved stimulated emission fluorescence depleti...
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A novel boron-containing π-conjugated compound has been synthesized by the introduction of electron-acceptors (dimesitylboron groups) at the 3,3'-positions of a carbazole dimer (electron-donor). The compound possesses excellent electrochemical properties and high fluorescence quantum yields. In addition, is a sensitive fluorescence sensor with remarkable colour changes and the results could ...
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ژورنال
عنوان ژورنال: New Journal of Chemistry
سال: 2017
ISSN: 1144-0546,1369-9261
DOI: 10.1039/c7nj00643h