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Cethrene: A Helically Chiral Biradicaloid Isomer of Heptazethrene.
Ravat, Prince; Solomek, Tomás; Rickhaus, Michel; Häussinger, Daniel; Neuburger, Markus; Baumgarten, Martin; Jurícek, Michal.
Afiliação
  • Ravat P; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland.
  • Solomek T; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland.
  • Rickhaus M; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland.
  • Häussinger D; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland.
  • Neuburger M; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland.
  • Baumgarten M; Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
  • Jurícek M; Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056, Basel, Switzerland. michal.juricek@unibas.ch.
Angew Chem Int Ed Engl ; 55(3): 1183-6, 2016 Jan 18.
Article em En | MEDLINE | ID: mdl-26593680
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article