Designing Tetraoxa[8]circulenes To Serve as Hosts and Sensors.

In D 4 -symmetric tetraoxa[8]circulenes, alternating fused benzene and furan rings form an octagonal array. These compounds are little known despite their novel properties, which include extended planar π-conjugation and a formally antiaromatic cyclooctatetraene core. Tetraoxa[8]circulenes can be formed by acid-induced cyclocondensations of suitable quinones, but existing methods often give very low yields. In addition, π-stacking of simple tetraoxa[8]circulenes reduces solubility and limits opportunities to form homogeneous mixtures or cocrystals with other compounds. To help make tetraoxa[8]circulenes more useful, we have developed better ways to synthesize them, and we have used these methods to produce awkwardly shaped derivatives with large concave electron-rich aromatic surfaces. These compounds crystallize to form open structures that can accommodate various guests, including C 60 . Analysis of the structures shows that the cyclooctatetraene core of the hosts exhibits surprising variations in C-C bond lengths and conjugation, which appear to be related to the gain or loss of aromaticity. This allows tetraoxa[8]circulenes to serve as sensitive probes of local molecular environment and to be used as sensors of electron-deficient species such as nitroaromatic compounds.