4-Aryl-2, 6-di(pyren-1-yl)pyridines: A facile procedure for synthesis and studying of fluorescence properties

Asaadi, Mohammad Reza; Behmadi, Hosein; Massoudi, Abdolhossein; Shaker, Mohammad

doi:10.30473/icc.2018.40457.1439

Document Type : Original Research Article

Authors

¹ Department of Chemistry, Faculty of Science, Payame Noor University, , PB BOX 19395-4697, Tehran, Iran

² Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran

³ Department of Chemistry, Faculty of Science, Payame Noor University

https://doi.org/10.30473/icc.2018.40457.1439

Abstract

Pyrene and its derivatives exhibit thermal stability, high extinction coefficients, excimer formation, high photoluminescence, long fluorescence lifetime, fluorophoric properties and enhanced charge carrier mobility which make them find applications in optoelectronic area and are useful as large planar synthetic building blocks in supramolecular chemistry. One of the approaches to overcome this downside is the introduction of bulky aryl/alkyl substituents or incorporation heteroatoms into the π-extended conjugated system of pyrene. In this work, Some new derivatives of 4-Aryl-2, 6-di(pyren-1-yl)pyridines have been synthesized through one-pot reaction and were formed with cyclization of Arylaldehydes, 1-acetylpyrene and ammonium acetate in acetic acid. The products were confirmed by FT-IR, Mass, 1H-NMR, 13C-NMR and elemental analysis. These new compounds were subsequently studied for their fluorescence properties.

Graphical Abstract

Keywords

Main Subjects

Organic chemistry

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Iranian chemical communication

4-Aryl-2, 6-di(pyren-1-yl)pyridines: A facile procedure for synthesis and studying of fluorescence properties

References

References

Volume 7, Issue 3, pp. 160-229, Serial No. 24
July 2019
Pages 214-221

4-Aryl-2, 6-di(pyren-1-yl)pyridines: A facile procedure for synthesis and studying of fluorescence properties

References

References

Volume 7, Issue 3, pp. 160-229, Serial No. 24July 2019Pages 214-221

Volume 7, Issue 3, pp. 160-229, Serial No. 24
July 2019
Pages 214-221