Hydrogen-Bond Controlled π-Dimerization in Viologen-Appended Calixarenes: Revealing a Subtle Balance of Weak Interactions.
The intramol. π-dimerization between two 4,4'-bipyridinium cation radicals directly connected to the wide rim of a calixarene is described. The ability of a phenol-contg. calixarene to dimerize in its two-electron-reduced state depends on a subtle balance of weak interactions assocd. with hydrogen bond formation on the lower rim and orbital overlap between π-radicals on the upper rim. [on SciFinder(R)]
Références
- Titre
- Hydrogen-Bond Controlled π-Dimerization in Viologen-Appended Calixarenes: Revealing a Subtle Balance of Weak Interactions.
- Type de publication
- Article de revue
- Année de publication
- 2015
- Auteurs
- Kahlfuss, Christophe, Milet Anne, Wytko Jennifer, Weiss Jean, Saint-Aman Eric, and Bucher Christophe
- Revue
- Org. Lett.
- Volume
- 17
- Pagination
- 4058–4061
- ISSN
- 1523-7052
Soumis le 12 avril 2018