Abstract
It is generally acknowledged that in protic organic solvents, 1,2-diamine reacts with 1,2-diketone to form an aromatic compound containing the pyrazine ring. As expected, the condensation reactions of 1,4-bis-[(triisopropylsilyl)ethynyl]naphthalene-2,3-diamine or 1,4-bis[(triisopropylsilyl)ethynyl]anthracene-2,3-diamine with 3,5-di-tert-butyl-1,2-benzoquinone yielded diazatetracene and diazapentacene derivatives. Meanwhile, naphthoazepin and anthroazepin derivatives which contained the imidazole ring were also obtained. Naphthoazepin and anthroazepin derivatives contained a seven-membered ring. All new compounds were characterized by proton and carbon-13 nuclear magnetic resonance spectroscopy, UV-vis spectrophotometry, high resolution mass spectrometry and single crystal X-ray diffraction. The possible reaction mechanisms were proposed as well.
| Translated title of the contribution | Different Pathways for the Cyclocondensation Reactions of 1,2-Diamine and 1,2-Diketone |
|---|---|
| Original language | Chinese (Traditional) |
| Pages (from-to) | 2686-2692 |
| Number of pages | 7 |
| Journal | Gaodeng Xuexiao Huaxue Xuebao/Chemical Journal of Chinese Universities |
| Volume | 39 |
| Issue number | 12 |
| DOIs | |
| State | Published - Dec 1 2018 |
Keywords
- Azacene
- Cyclo-condensation reaction
- Organic semiconductor
- Ring expansion
- Single-crystal structure
ASJC Scopus subject areas
- General Chemistry
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