4.8 Article

Cethrene: A Helically Chiral Biradicaloid Isomer of Heptazethrene

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 55, Issue 3, Pages 1183-1186

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201507961

Keywords

biradicaloids; cethrene; chirality; helical structures; zethrene

Funding

  1. Swiss National Science Foundation (SNF) [M.J./PZ00P2_148043, D.H./200021_130263]
  2. Novartis University of Basel Excellence Scholarship for Life Sciences
  3. Experientia Foundation
  4. German Science Foundation (DFG) [M.B./SFB/TR49]
  5. Swiss National Science Foundation (SNF) [200021_130263, PZ00P2_148043] Funding Source: Swiss National Science Foundation (SNF)

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We report the synthesis and properties of cethrene, the only helically chiral isomer of heptazethrene with a biradicaloid singlet ground state. Cethrene gives a well-resolved EPR spectrum at room temperature and its structure was confirmed by 2D NMR and absorption spectroscopies. Our experiments and calculations show that the helical twist affects its electronic properties and decreases the singlet-triplet energy gap when compared to that of planar heptazethrene. Cethrene undergoes an intramolecular cyclization within several hours at room temperature.

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