(E)-2-(6-(4′-(Diphenylamino)-[1,1′-biphenyl]-2-yl)-[1,2,5]oxadiazolo[3,4-b]pyrazin-5(4H)-ylidene)-2-(6-(4′-(diphenylamino)-[1,1′-biphenyl]-2-yl)-[1,2,5]oxadiazolo[3,4-b]pyrazin-5-yl)acetonitrile

IF 0.6 Q4 CHEMISTRY, ORGANIC Molbank Pub Date : 2023-08-21 DOI:10.3390/m1714
Y. Kvashnin, P. Slepukhin, D. Gazizov, E. F. Zhilina, G. Rusinov, E. Verbitskiy, V. Charushin
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Abstract

[1,2,5]Oxadiazolo[3,4-b]pyrazines are of great interest due to their promising photophysical and electrochemical properties, as well their potential use in a wide range of electronic devices. Herein, we report on the preparation of the unexpected product derived from the interaction of 2′-([1,2,5]oxadiazolo[3,4-b]pyrazin-5-yl)-N,N-diphenyl-[1,1′-biphenyl]-4-amine with 2-cyanoacetic acid under basic conditions. The resulting product was characterized using 1H and 13C NMR spectra, high resolution mass spectrometry, Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction analyses. Furthermore, its photophysical and electrochemical properties were studied using cyclic voltammetry, UV–Vis, and emission spectroscopy. The experimental results have been further rationalized through theoretical DFT calculations.
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(E) -2-(6-(4′-(二苯基氨基)-[1,1′-联苯]-2-基)-[1,2,5]恶二唑并[3,4-b]吡嗪-5(4H)-亚基)-2-(6-
[1,2,5]恶二唑并[3,4-b]吡嗪由于其具有良好的光物理和电化学性质,以及在广泛的电子设备中的潜在用途而引起人们的极大兴趣。本文报道了在碱性条件下,2′-([1,2,5]恶二唑并[3,4-b]吡嗪-5-基)-N,N-二苯基-[1,1′-联苯]-4-胺与2-氰基乙酸相互作用产生的意想不到的产物的制备。使用1H和13C NMR光谱、高分辨率质谱、傅立叶变换红外光谱(FTIR)和X射线衍射分析对所得产物进行表征。此外,利用循环伏安法、紫外-可见光谱法和发射光谱法研究了其光物理和电化学性质。实验结果通过理论DFT计算得到了进一步的合理化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molbank
Molbank Chemistry-Physical and Theoretical Chemistry
CiteScore
0.70
自引率
33.30%
发文量
174
审稿时长
11 weeks
期刊介绍: •organic synthesis •biosynthesis •extraction and purification •natural product derivatives •structural elucidation (X-ray crystallography, NMR, etc.)
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