Citation: P.Krinochkin Alexey, S. Kopchuk Dmitry, V. Chepchugov Nikolay, A. Kim Grigory, S. Kovalev Igor, Rahman Matiur, V. Zyryanov Grigory, Majee Adinath, L. Rusinov Vladimir, N. Chupakhin Oleg. An efficient synthetic approach towards new 5, 5'-diaryl-2, 2'-bipyridine-based fluorophores[J]. Chinese Chemical Letters, ;2017, 28(5): 1099-1103. doi: 10.1016/j.cclet.2016.12.043 shu

An efficient synthetic approach towards new 5, 5'-diaryl-2, 2'-bipyridine-based fluorophores

a.
Ural Federal University, Yekaterinburg 620002, Russian Federation
b.
Postovsky Institute of Organic Synthesis of RAS(Ural Division), Yekaterinburg 620990, Russian Federation
c.
Department of Chemistry, Visva-Bharati(A Central University), Santiniketan 731235, India

Corresponding author: S. Kopchuk Dmitry, dkopchuk@mail.ru
Received Date: 14 October 2016
Revised Date: 28 November 2016
Accepted Date: 6 December 2016
Available Online: 8 May 2017

Figures(3)

An efficient approach has been developed for the synthesis of 5, 5'-diaryl-2, 2'-bipyridines via their 1, 2, 4-triazine analogues. The notable advantages of the present method are:The possibility of varying the aromatic substituents in the positions 5 and 5' of bipyridine core and the possibility for obtaining 2, 2'-bipyridines bearing a fused cyclopentene core to increase the solubility in organic solvents. These 5, 5'-diaryl-2, 2'-bipyridines exhibited an intense emission in a range of ca. 422-521 nm in acetonitrile solution; depending on the nature of the aromatic substituents and the presence of annulated cyclopentene fragments. Apart from that, the significant bathochromic shifts of the both absorption and emission maxima were observed in comparison with a number of previously described similar structures. In some cases the significant increasing of the fluorescence quantum yields took place.
- 2, 2'-Bipyridines,
- 1, 2, 4-Triazines,
- Aza-Diels-Alder reaction,
- Fluorescence
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