| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219828 | Tetrahedron | 2012 | 6 Pages |
Abstract
A mild and effective method to prepare 2,7-dibromo-4,5-diazafluoren-9-one (3) has been described involving tandem oxidation and rearrangement reactions. Diazafluorenone-based donor–acceptor (p–n) molecules via stille coupling reactions exhibit solvent-dependent fluorescence and excellent self-assembly behaviors at the solid–liquid interface according to the characterization of scanning tunneling microscopy (STM).
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