New design of cyclotriphosphazene derivatives bearing carbazole units: The syntheses, characterization, and photophysical properties
Özet
In the current work, di- and tetra- aniline substituted cyclotriphosphazene derivatives (1a-b) were prepared from commercially available cyclotriphosphazene and underwent nucleophilic substitution reaction with 9-ethyl-9Hcarbazol-3-ol (2) to produce three new cyclotriphosphazene compounds having two- (3a), three- (4b) and fourcarbazole units (5b), respectively. The full characterization data of the targeted compounds were obtained by utilizing elemental analysis, mass spectrometry, H-1, and P-31 NMR spectroscopies. The structure of compound 3a was further supported by single crystal X-Ray diffraction technique. As the photophysical aspect of the synthesized compounds 3a, 4b and 5b, UV- Vis and steady-state fluorescence spectroscopies were used in different organic solvents. In addition, time-resolved fluorescence and 3D-fluorescence spectroscopies were applied to get deeper information about the photophysical properties of targeted compounds.
Sürdürülebilir Kalkınma Amaçları
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SKA 2: Açlığa Son
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SKA 3: Sağlıklı Bireyler
Atıf için künye
Palabiyik, D., Balci, C. M., Tümay, S. O., Sengul, I. F., & Besli, S. (2022). New design of cyclotriphosphazene derivatives bearing carbazole units: The syntheses, characterization, and photophysical properties. Inorganica Chimica Acta, 539. https://doi.org/10.1016/j.ica.2022.121022
BibTeX
@article{palabiyik2022-80565,
author = {Palabiyik, Duygu and Balci, Ceylan Mutlu and Tümay, Süreyya Oğuz and Sengul, Ibrahim F. and Besli, Serap},
title = {New design of cyclotriphosphazene derivatives bearing carbazole units: The syntheses, characterization, and photophysical properties},
journal = {Inorganica Chimica Acta},
year = {2022},
volume = {539},
issn = {0020-1693},
doi = {10.1016/j.ica.2022.121022},
url = {https://akademik.atauni.edu.tr/yayinlar/80565-new-design-of-cyclotriphosphazene-derivatives-bearing-carbazole-units-the}
}