Hydrogen‐bonded block mesogens derived from semiperfluorinated benzoic acids and the non‐mesogenic 1,2‐bis(4‐pyridyl)ethylene

Abstract

Thermal properties of benzoic acids carrying one or two semiperfluorinated alkoxy tails on the aromatic core have been investigated in binary mixtures with the non‐liquid crystalline bidirectional trans‐1,2‐bis(4‐pyridyl)ethylene. The hydrogen bonded complexes built from the complementary molecular species show a significantly enhanced mesophase stability compared with the fluorinated acids in their pure states. The mesophase morphologies of the complexes are governed mainly by the number of the partially fluorinated chains grafted to the acid component. Mixed systems comprising the one‐chain acids exhibit a smectic C phase followed by a smectic A phase at more elevated temperatures. Incorporation of a second semiperfluorinated chain into the acid leads to the formation of columnar mesophases. These columnar phases of the H‐bonded complexes should represent ribbon phases resulting from the collapse of the smectic layers.

Acknowledgement

This work was supported by the Land Brandenburg, Germany, and the Fonds der Chemischen Industrie. We are very grateful to B. Smarsly for kind support in performing X‐ray measurements at the Max Planck Institute of Colloids and Interfaces, Potsdam‐Golm, Germany.