Marzieh Rabiei - Academia.edu (original) (raw)
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Papers by Marzieh Rabiei
International Journal of Advanced Science and Engineering, 2019
In this study preparation and thermal, electrochemical, photophysical properties of the compounds... more In this study preparation and thermal, electrochemical, photophysical properties of the compounds are reported. New series of compounds consisting of 4-Allylamino-N-4-aminobenzenesulfonamide-1,8-naphthalimide, 4-Amino-N-4-amino-N-(2-pyrimidinyl) benzenesulfonamide-1,8-naphthalimide and 4-Allylamino-N-4-amino-N-(2-pyrimidinyl) benzenesulfonamide-1,8-naphthalimide were synthesized via sonic method from intermediate 4-nitro-1,8-naphthalimide by imidation, reduction and allylation reactions. These compounds were characterized by thin layer chromatography (TLC), differential scanning calorimetry (DSC), fourier transform infrared spectroscopy (FT-IR), 1 H-nuclear magnetic resonance (1 HNMR), 13 C-NMR, liquid chromatography, UV-Vis spectroscopy and fluorimetry. New acceptor-donor compounds were obtained with the photoluminescence quantum yields (PLQY) of 33.68-79.70% in solution and 0.85-3.39% in non-doped solid film. The synthesized dyes absorb electromagnetic radiation in the range of 434-440 nm and emit solid films exhibited fluorescence in the range of 561-614 nm. The ionization potentials of the synthesized dyes were found to range from 6.00 eV to 6.09 eV.
International Journal of Advanced Science and Engineering, 2019
In this study preparation and thermal, electrochemical, photophysical properties of the compounds... more In this study preparation and thermal, electrochemical, photophysical properties of the compounds are reported. New series of compounds consisting of 4-Allylamino-N-4-aminobenzenesulfonamide-1,8-naphthalimide, 4-Amino-N-4-amino-N-(2-pyrimidinyl) benzenesulfonamide-1,8-naphthalimide and 4-Allylamino-N-4-amino-N-(2-pyrimidinyl) benzenesulfonamide-1,8-naphthalimide were synthesized via sonic method from intermediate 4-nitro-1,8-naphthalimide by imidation, reduction and allylation reactions. These compounds were characterized by thin layer chromatography (TLC), differential scanning calorimetry (DSC), fourier transform infrared spectroscopy (FT-IR), 1 H-nuclear magnetic resonance (1 HNMR), 13 C-NMR, liquid chromatography, UV-Vis spectroscopy and fluorimetry. New acceptor-donor compounds were obtained with the photoluminescence quantum yields (PLQY) of 33.68-79.70% in solution and 0.85-3.39% in non-doped solid film. The synthesized dyes absorb electromagnetic radiation in the range of 434-440 nm and emit solid films exhibited fluorescence in the range of 561-614 nm. The ionization potentials of the synthesized dyes were found to range from 6.00 eV to 6.09 eV.