Influence of a long-chain alkane on the photoinduced nematic-isotropic transition

We investigated the phenomenon of photoinduced nematic-isotropic (N-I) transition for different concentrations of a long-chain alkane, viz., octadecane (OD), and a host liquid crystalline material having a small quantity (4.5 mol %) of a photoactive azo compound. As expected, the N-I transition temperature diminishes with increasing concentration of OD. Data of time-resolved measurements of the dielectric constant through both the UV-activated trans-cis transformation and the thermal back relaxation process are presented. With increasing concentration of OD, although the response time for the former process increases slightly by less than a factor of 2, the thermal back relaxation shows a greater increase by more than an order of magnitude. As a possible explanation for this surprising result, we discuss an argument based on the structural incompatibility of the constituents of the system investigated.