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Updated: Dec 21, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
New reactions of a dibenzo[a,e]pentalene
Masaichi Saito1, Michio Nakamura, Tomoyuki Tajima
1Department of Chemistry, Graduate School of Science and Engineering, Saitama University, Shimo-okubo, Sakura-ku, Saitama-city, Saitama, 338-8570, Japan. masaichi@chem.saitama-u.ac.jp
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.
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