Microscopic structure of aqueous alkylamine mixtures: A computer simulation study
We examine the microscopic origin of the pronounced x-ray scattering pre-peaks observed in water-rich aqueous alkylamine mixtures. While neat amines display weak pre-peaks compared to alcohols, and aqueous alcohols generally exhibit none, aqueous amines display a striking and unexpected signal. Molecular dynamics simulations of primary amines from propylamine to octylamine show that nitrogen head groups preferentially saturate the surfaces of water-rich domains, stabilizing both water and amine regions through water-nitrogen donor hydrogen bonding. This interfacial anchoring prevents macroscopic demixing except at high water contents, where too few amines remain to cover the interfaces. The resulting disordered bilayer-like arrangement generates long-ranged domain oscillations that appear as positive like-like species and negative cross species correlations, whose partial cancellation produces the experimental pre-peak. Model comparisons further show that the effect is highly sensitive to both solute and water force fields, with the CHARMM-AA/SPC/E combination offering the most consistent description. These results establish aqueous amines as prototypical systems in which stable micro-heterogeneity and supramolecular topology directly give rise to scattering pre-peaks, providing a concrete bridge between molecular liquids and micro-emulsions.
Authors
- Aurélien Perera (ORCID: https://orcid.org/0000-0001-9119-6659)
- Martina Požar (ORCID: https://orcid.org/0000-0001-6300-2204)
- Bernarda Lovrinčević
- Lena Friedrich
- Christian Sternemann
Institutions
- Centre National de la Recherche Scientifique (FR)
- TU Dortmund University (DE)
- Sorbonne Université (FR)
- Laboratoire de Physique Théorique de la Matière Condensée (FR)
- University of Split (HR)
Publication Details
- Journal
- The Journal of Chemical Physics
- Published
- 2026-02-03
- DOI
- https://doi.org/10.1063/5.0305130
- Primary Topic
- Spectroscopy and Quantum Chemical Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00