AbstractAcrylic acid-modified polyhedral oligomeric silsesquioxane (AC-POSS) was synthesized by the reaction between the amine groups in polyhedral oligomeric silsesquioxane (POSS) and acrylic acid, which could dissolve in water and can be easily purified. Free-radical copolymerization was applied to synthesize azobenzene liquid crystalline polymer silsesquioxane (LCP-POSS) with different proportions of AC-POSS and liquid crystalline monomers. The trans-isomers of azobenzene moieties in LCP-POSS were gradually transformed to cis-isomers with increasing ultraviolet irradiation time. The photoisomerization reaction of liquid crystalline polymer (LCP) and LCP-POSS showed the first-order dynamic reaction. Compared with the LCP, the photoisomerization rate constant of LCP-POSS was decreased due to the space steric hindrance of the POSS as a rigid segment. The phase transition temperature of liquid crystalline in LCP-POSS increased with increasing POSS content, and the liquid crystalline texture in LCP-POSS became smaller under the polarized light. With further increasing the POSS content (>50 wt%) in LCP-POSS, the ordered structure of the liquid crystalline phase was gradually affected, resulting in one-way liquid crystal (LC) phase behavior. The synthesized LCP-POSS has LC properties, light-responsive properties, and thermal stability. When the POSS is introduced into the LC material, the phase state of the LC material will become more abundant and the LC phase will become more stable. The significance of this study is to develop and extend its applications as stimuli-responsive materials and devices.
Spatial reorientation of azobenzene side groups of a liquid crystalline polymer induced by linearly polarized light