Gas phase synthesis of [4]-helicene.

ABSTRACT: A synthetic route to racemic helicenes via a vinylacetylene mediated gas phase chemistry involving elementary reactions with aryl radicals is presented. In contrast to traditional synthetic routes involving solution chemistry and ionic reaction intermediates, the gas phase synthesis involves a targeted ring annulation involving free radical intermediates. Exploiting the simplest helicene as a benchmark, we show that the gas phase reaction of the 4-phenanthrenyl radical ([C₁₄H₉]^•) with vinylacetylene (C₄H₄) yields [4]-helicene (C₁₈H₁₂) along with atomic hydrogen via a low-barrier mechanism through a resonance-stabilized free radical intermediate (C₁₈H₁₃). This pathway may represent a versatile

SUBMITTER: Zhao L 

PROVIDER: S-EPMC6447558 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature