Structure–Property Relationships for n-Alkylamine and Aliphatic Carboxylic Acid-Derived Thermomorphic Multiphase Systems

Thuruthel Kuriakose, Megha, Shahbaz, Kaveh, and Weber, Cameron C. (2026) Structure–Property Relationships for n-Alkylamine and Aliphatic Carboxylic Acid-Derived Thermomorphic Multiphase Systems. ChemSusChem, 19 (17). e71019.

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Abstract

Thermomorphic multiphase systems (TMS) are liquids that display abrupt and reversible changes in miscibility with temperature. TMS based on mixtures of amines and carboxylic acids have been found to exhibit lower critical solution temperature (LCST) behavior, although prior examples have relied on clinical anesthetics as the amine component due to poor understanding of the relationship between the amine structure and LCST behavior. Here, the role of the amine partner of the TMS was systematically investigated, utilizing an array of primary, secondary, and tertiary amines in combination with aliphatic carboxylic acids. Systems featuring tripropylamine (TPA) or dibutylamine (DBA) were uniquely capable of displaying thermoswitchable behavior in the presence of a sufficiently hydrophobic aliphatic carboxylic acid, whereas primary amines and other secondary and tertiary amines investigated did not form TMS. TMS formation could be related to macroscopic hydrophilicity parameters for the amines, providing a foundational basis for future TMS design, and their ability to facilitate extractions was demonstrated. These findings highlight the potential to prepare TMS from scalable, low-cost amines toward the development of environmentally benign switchable solvent systems.

Item ID: 93938
Item Type: Article (Research - C1)
ISSN: 1864-5631
Keywords: amines, dye extraction, fatty acids, lower critical solution temperature, phase transition, switchable solvents, thermomorphic multiphase systems
Copyright Information: This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Date Deposited: 10 Nov 2026 23:29
FoR Codes: 34 CHEMICAL SCIENCES > 3405 Organic chemistry > 340504 Organic green chemistry @ 100%
SEO Codes: 17 ENERGY > 1799 Other energy > 179999 Other energy not elsewhere classified @ 100%
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