Gekreuzt konjugierte oligomere aus pyrrol-, benzol- und carbonyl-Bausteinen

Chalcones can serve as C2 or C3 components for the formation of 1H-pyrroles. In particular the reaction with tosylisocyanid could be applied to the oligochalcones with up to 6 enone units. A series of cross-conjugated oligomers was obtained; these compounds consist of a chain of 1,4-phenylene, carbonyl and 1H-pyrrole-3,4-diyl building blocks. The benzene rings bear two propoxy sidechains in order to enhance the solubility.