Synthesis, photophysical and electrochemical properties of pyridine, pyrazine and triazine-based (D–π–)₂A fluorescent dyes

Scholarly Works

• Zhang, T.; Feng, C.; Li, A.; Zhu, Y.; Jin, C.; Na, H.; Liu, F.; Zhu, J. Fabrication of microfibrillated cellulose from biomass by use of carbon nitride with high nitrogen/carbon ratio. International journal of biological macromolecules 2024, 277, 133729. doi:10.1016/j.ijbiomac.2024.133729
• Alshubramy, M. A.; Alam, M. M.; Alamry, K. A.; Asiri, A. M.; Hussein, M. A.; Rahman, M. M. Ionic Organic Network-based C3-symmetric@Triazine core as a selective Hg+2 sensor. Designed monomers and polymers 2024, 27, 35–50. doi:10.1080/15685551.2024.2360746
• Verbitskiy, E. V.; Lipunova, G. N.; Nosova, E. V.; Charushin, V. N. Advances in the design of functionalized 1,4-diazines as components for photo- or/and electroactive materials. Dyes and Pigments 2023, 220, 111763. doi:10.1016/j.dyepig.2023.111763
• Seck, I.; Sall, M. L.; Ndiaye, A.; Ndoye, S. F.; Ba, L. A.; Seck, M. Spectroscopic Electrochemical Properties and DFT Calculation of 1-Aryltriazenes. International Journal of Organic Chemistry 2023, 13, 109–128. doi:10.4236/ijoc.2023.134009
• Seck, I. Spectroscopic Electrochemical Properties and Dft Calculation of 1-Aryltriazenes. Elsevier BV 2023. doi:10.2139/ssrn.4479459
• Nosova, E. V.; Lipunova, G. N.; Zyryanov, G. V.; Charushin, V. N.; Chupakhin, O. N. Functionalized 1,3,5-triazine derivatives as components for photo- and electroluminescent materials. Organic Chemistry Frontiers 2022, 9, 6646–6683. doi:10.1039/d2qo00961g
• Takemura, K.; Imato, K.; Ooyama, Y. Mechanofluorochromism of (D-π-)2A-type azine-based fluorescent dyes. RSC advances 2022, 12, 13797–13809. doi:10.1039/d2ra02431d
• Verbitskiy, E. V.; Rusinov, G. L.; Chupakhin, O. N.; Charushin, V. N. Azines as unconventional anchoring groups for dye-sensitized solar cells: The first decade of research advances and a future outlook. Dyes and Pigments 2021, 194, 109650. doi:10.1016/j.dyepig.2021.109650
• Hiebel, M.-A.; Suzenet, F. Triazines, tetrazines, and fused ring polyaza systems. Progress in Heterocyclic Chemistry; Elsevier, 2021; pp 467–499. doi:10.1016/b978-0-323-89812-6.00014-6
• Jadhav, C. K.; Nipate, A. S.; Chate, A. V.; Patil, A. P.; Gill, C. H. Ionic liquid catalyzed one-pot multi-component synthesis of fused pyridine derivatives: A strategy for green and sustainable chemistry. Journal of Heterocyclic Chemistry 2020, 57, 4291–4303. doi:10.1002/jhet.4135
• Olutas, M.; Sağırlı, A. Solvatochromic and solid-state emissive azlactone-based AIEE-active organic dye: Synthesis, photophysical properties and color-conversion LED application. Journal of Molecular Liquids 2020, 313, 113482. doi:10.1016/j.molliq.2020.113482
• Tsuchiya, Y.; Yamaguchi, K.; Miwa, Y.; Kutsumizu, S.; Minoura, M.; Murai, T. N,N-Diarylthiazol-5-amines: Structure-Specific Mechanofluorochromism and White Light Emission in the Solid State. Bulletin of the Chemical Society of Japan 2020, 93, 927–935. doi:10.1246/bcsj.20200083
• Hiebel, M.-A.; Suzenet, F. Triazines, Tetrazines, and Fused Ring Polyaza Systems. 2019; Vol. 31, pp 467–499.

Explore citations to this article at