Takudrei

097
Oligothiophene-Based Catenanes: Synthesis and Electronic Properties of a Novel Conjugated Topological Structure

M. Ammann, M. Wilde, G. Götz, E. Mena-Osteritz, A. Rang, C. A. Schalley, P. Bäuerle— 2006

Make it a double: A double metal template strategy has been used to form a “π-conjugated catenane” consisting of intertwined macrocycles with oligothienyl and phenanthroline units (see calculated structure). The optical and redox properties as well as the structural and conformational analyses give clear evidence that the two macrocycles in the catenane influence each other by through-space donor–acceptor interactions.

Title097
Oligothiophene-Based Catenanes: Synthesis and Electronic Properties of a Novel Conjugated Topological Structure
AuthorM. Ammann, M. Wilde, G. Götz, E. Mena-Osteritz, A. Rang, C. A. Schalley, P. Bäuerle
Date20061031
IdentifierDOI 10.1002/anie.200602652, 10.1002/ange.200602652
Source(s)
CitationAngew. Chem. Int. Ed. 2007, 46, 363-368; Angew. Chem. 2007, 119, 367-372