| Literature DB >> 27897398 |
Zhe Sun1,2, Naoya Miyamoto3, Sota Sato1,4, Hidetoshi Tokuyama3, Hiroyuki Isobe1,2,4.
Abstract
The invention of corner units was the key factor that allowed the synthesis of cyclo-para-phenylenes with strained curved π-systems. Despite only a few scarce instances of the development of corner units to date, a variety of structural congeners have been synthesized. These preceding corner units commonly possessed directing angles of ≤90°, which enabled the macrocyclization of multiple units, up to six. In this study, we introduce an obtuse-angled corner unit for the synthesis of cyclo-para-phenylene congeners. The corner unit with oxanorbornadiene possessed a directing angle of 126° and thus allowed for the macrocyclization of larger structures with up to seven units. Reductive aromatization was applicable to complete the cyclo-para-phenylene structures and afforded the congeners with multiple anthracenylene panels. Structural studies with experimental and theoretical methods revealed a fluctuating structure with an intrinsic non-belt shape.Entities:
Keywords: anthracenylene; carbon nanohoop; macrocycles; oxanorbornadiene; structure elucidation
Year: 2016 PMID: 27897398 DOI: 10.1002/asia.201601614
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X