Abstract:
The differences in the kinetics of the polymorphic transformation of crystallographic phases of n-alkanes of different parities: tricosane Ñ$_{23}$Í$_{48}$ and tetracosane Ñ$_{24}$Í$_{50}$ were studied using Fourier transform infrared spectroscopy. It has been established that a first-order structural phase transition occurs with a change in the symmetry type of the initial orthorhombic or triclinic subcells to hexagonal ones through the formation of a number of intermediate rotator phases $(R_I, R_{II}, R_V)$ depending on the symmetry of the molecules (cis or trans).
Keywords:n-alkanes, lamellae, phase transitions, rotator phases, IR spectroscopy.