Abstract
Reduction of dibenzo[a,e]pentalene 3 (denoted as dibenzopentalene hereafter) with excess lithium gave dilithium dibenzopentalenide 1. Since oxidation of 1 with iodine gave 3, redox behavior between 1 and 3 is controllable and reversible. Reaction of 3 with methyllithium gave lithium 5-methyldibenzopentalenide 5, the formation of which was evidenced by some trapping experiments and X-ray crystallographic analysis. Reactions of 3 with halogens gave 5,10-dihalodibenzopentalenes, 8 and 9. Some optical properties of novel dibenzopentalene derivatives are also demonstrated.
Original language | English |
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Pages (from-to) | 6062-6068 |
Number of pages | 7 |
Journal | Chemistry - A European Journal |
Volume | 14 |
Issue number | 20 |
DOIs | |
Publication status | Published - Jul 7 2008 |
Externally published | Yes |
Keywords
- Anions
- Aromatic compounds
- Emission spectroscopy
- Reduction
- UV/Vis spectroscopy
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry