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Inside Cover Oligothiophene-Based Catenanes Synthesis and Electronic Properties of a Novel Conjugated Topological Structure (Angew. Chem. Int. Ed. 32007)

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Inside Cover
Peter Buerle,* Martin Ammann, Markus Wilde, Gnther Gtz,
Elena Mena-Osteritz, Alexander Rang, and Christoph A. Schalley
A “p-conjugated catenane” or more accurately a catenane formed from two
intertwined conjugated macrocycles has been formed for the first time by a double
metal template strategy. Interestingly, a through-space electronic interaction between
the donor unit (oligothiophene, metallic color) and the acceptor component of the
other ring (phenanthroline, blue) is evident. Further details can be found in the
Communication by P. B!uerle et al. on page 363 ff.
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properties, electronica, 32007, oligothiophene, base, int, catenane, cover, structure, angel, synthesis, chem, conjugate, insider, novem, topological
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