Insight from high-pressure dielectric studies into molecular dynamics of the itraconazole-glycerol mixture in smectic and isotropic phases

• Main Authors: Kramarczyk, D. (Author), Musiał, M. (Author), Paluch, M. (Author), Rams-Baron, M. (Author)
• Format: Article
• Language: English
• Published: American Institute of Physics Inc. 2022
• Subjects: Activation energy; Broadband dielectric spectroscopy; chemistry; Dielectric studies; Equations of state; glycerol; Glycerol; High pressure; Isotropic phasis; itraconazole; Itraconazole; liquid crystal; Liquid Crystals; Mixtures; molecular dynamics; Molecular dynamics; Molecular Dynamics Simulation; Phase diagrams; phase transition; Phase Transition; Phase transitions; Relaxation dynamics; Relaxation processes; Smectic A phase; Smectic phase; Smectic-A; Spectroscopy measurements; Temperature
• Online Access: View Fulltext in Publisher

 We present here the results of high-pressure broadband dielectric spectroscopy (BDS) measurements for a mixture of liquid-crystalline drug itraconazole (ITZ) and glycerol (GLY) at a critical concentration of 5% w/w in which the nematic order is eliminated. In the investigated system, smectic-A to isotropic phase transition leaves a clear fingerprint on the dielectric response, allowing for a phase diagram creation using BDS data. By following the α-relaxation dynamics under different thermodynamic conditions, we provide insights into the effect of pressure on temperature and the phenomenology of smectic-A to the isotropic phase transition. Additional measurements of specific volume as a function of pressure and temperature provide us with a deeper insight into material properties that could be analyzed comprehensively via the equation of state. We proved the validity of the density scaling concept, showing that the mixture's complexity does not exclude thermodynamic scaling of dynamic properties related to the α-process in the smectic-A phase. The low value of scaling exponent γ = 2.00 ± 0.02 and a high ratio of the activation energy at constant volume, EV, to the activation enthalpy at constant pressure, HP, indicate that temperature is a dominant variable controlling α-relaxation dynamics in the ordered smectic-A phase of the ITZ-GLY mixture. © 2022 Author(s).