Affiliation:
1. Department of Applied Chemistry, Graduate School of Engineering Osaka University Suita Japan
2. Innovative Catalysis Science Division, Institute for Open and Transdisciplinary Research Initiatives (ICS‐OTRI) Osaka University Suita Japan
3. Center for Atomic and Molecular Technologies, Graduate School of Engineering Osaka University Suita Japan
Abstract
AbstractThe chemistry of nonalternant hydrocarbons has recently experienced a considerable resurgence. As the relationship between naphthalene and azulene shows, an important design concept for a nonalternant framework is to replace the two hexagons of an alternant system with a pentagon and heptagon pair. The pursuit of the nonalternant isomers of pyrene, which has seven possible nonalternant isomers, has been the most significant related project. Through enormous dedication by many pioneering works, six of the seven possible nonalternant isomers of pyrene have been isolated and characterized as stable aromatic molecules, differentiating themselves from pyrene in terms of optoelectronic properties. However, the only unsynthesized isomer, bis‐periazulene (cyclohepta[def]fluorene), had remained an uncharacterized hydrocarbon until 2022, despite many synthetic and theoretical investigations since it was first reported in 1955. In this review, we summarize the chemistry of the pyrene's nonalternant isomers, including our recent achievements in synthesizing and characterizing bis‐periazulene derivatives. The historical perspectives, synthetic approaches, fundamental properties, and comparisons to related systems are documented.
Funder
Japan Society for the Promotion of Science
Ministry of Education, Culture, Sports, Science and Technology
Core Research for Evolutional Science and Technology
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Cited by
17 articles.
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