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The first examples of liquid crystalline pyrimidine-based photo-switchable bent-core monomers incorporating azobenzene as side arms linked with terminal double bonds as polymerizable functional groups are synthesized and characterized. Polarizing optical microscopy (POM), differential scanning calorimetry (DSC) and X-ray diffraction analysis reveal that the bent-shaped lower homologue compounds are crystalline in nature whereas higher homologue compounds display the stable enantiotropic B 6 phase. They exhibit fast photoisomerization effects in solution and relatively slow photoisomerization effects in liquid crystal cells. In solution both trans-cis and cis-trans occur at around 3 s and 200 s, respectively, whereas in solids they occur at around 10 s to 200 min. These are some of the first examples of azobenzene liquid crystals which exhibit very fast switching properties in solutions.

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