Broadband dielectric spectroscopy and rheology reveal supramolecular formation in van der Waals liquids, indicating significant dipole–dipole interactions.
Non-hydrogen bonding van der Waals liquids with dipole–dipole interactions are typically viewed as non-associative and not considered able to sustain large supramolecular structures. Combining broadband dielectric spectroscopy (BDS) and rheology, we demonstrate the supramolecular formation in a group of non-hydrogen bonding van der Waals liquids, i.e., 1-bromo-2-ethylhexane, 1-chloro-2-ethylhexane, and 1-bromo-3,7-dimethyloctane. BDS shows an emergence of a Debye-like process slower than their structural relaxation, which follows super-Arrhenius temperature dependence. Meanwhile, rheological measurements reveal a noticeable dynamical separation between the terminal relaxation and the structural rearrangements. Interestingly, the rheological terminal time agrees remarkably well with the dielectric Debye-like relaxation time, pointing to a strong coupling between the terminal flow and the supramolecular dynamics of these van der Waals liquids. These results highlight a key role of intermolecular dipole–dipole interaction in the supramolecular structure formation and the slow dynamics of van der Waals liquids.
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Patil et al. (2025) studied this question.
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