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
Revue
Org. Lett.
Volume
17
Pagination
4058–4061
ISSN
1523-7052
Soumis le 12 avril 2018