Abstract
The novel spiro-twins 3a–f were prepared in three steps by one-pot oxidative coupling of guaiacol (9) and 1,2-dialkoxybenzenes 10a–f, followed by demethylation of the triphenylene 11 and subsequent etherification with the tetrabromide 6. A related strategy gave the tetramers 7a–f in two steps. Whereas derivatives 3a,b and 7a,b with pentyloxy and hexyloxy chains showed isotropic melting behavior, compounds 3c–f and 7c–f with longer alkyl chains displayed columnar mesophases. DSC, polarizing microscopy, X-ray diffraction and molecular modeling studies were used to further characterize the type of mesophase. For the spiro-twin 3 either a rectangular or a hexagonal columnar phase were conceivable. In case of 7f a hexagonal columnar mesophase was assigned.
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