“…The molecular relaxation rate, is related to the parameters β and γ by eq A significant body of literature indicates that collective dynamics of supramolecular hydrogen-bonded networks give rise to slow, dielectric relaxations in neat HBDs such as monohydroxy alcohols, secondary amides, water, glycerol, and imidazoles, among others. ,− The strengths of intermolecular interactions as well as the sizes and orientations of the supramolecular dipoles determine the effective dipole moments and the rates of the slow “Debye-like” relaxations. ,, The term “Debye-like” is often employed because the spectral shapes observed for such slow processes are close to those of an ideal dielectric relaxation initially derived by Peter Debye. , Extensive studies of different HBDs have revealed the existence of different types of supramolecular hydrogen-bonded structures, with the preferred orientations being sensitive to the molecular structure, pressure, and temperature. ,, To account for dipolar contributions, the spectra are fit using the empirical Havriliak–Negami equations which are well established for describing reorientation polarization. By correlating this information with the knowledge of the functional molecular groups present, a more complete understanding of the system can be obtained.…”