4.6 Article

Nanostructure in Amphiphile-Based Deep Eutectic Solvents

Journal

LANGMUIR
Volume 39, Issue 47, Pages 16776-16784

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.3c02105

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This study investigates the nanostructure of deep eutectic solvents (DESs) composed of different sulfobetaines and camphor sulfonic acid, as well as their interactions with water and dodecane. Small angle neutron scattering experiments reveal that water and dodecane interact with the hydrophilic and hydrophobic moieties in the DES structure, causing the entire structure to swell and solvate. This research has the potential to provide new templating methods for growing inorganic or polymeric materials using DESs.
Deep eutectic solvents (DESs) are an emerging class of modern, often green solvents with unique properties. Recently, a deep eutectic system based on amphiphilic surfactant N-alkyl-N,N-dimethyl-3-ammonio-1-propanesulfonate (C12 & C14 sulfobetaine) and (1S)-(+)-10-camphor-sulfonic acid in the molar ratio 1:1.5 has been reported. Nanostructuring can be expected in this DES due to the nature of the components. In this work, we have investigated the native nanostructure in the DES comprising C12-C18 alkyl chain sulfobetaines with camphor sulfonic acid and how it interacts with polar and nonpolar species, water and dodecane, respectively, using small angle neutron scattering. By using contrast variation to highlight the relative position of the solvent components and additives, we can resolve the structure of the solvent and how it changes upon interaction with water and dodecane. Scattering from the neat DES shows structures corresponding to the self-assembly of sulfobetaines; the size of the structure increases as the alkyl chain length of the sulfobetaines increases. Water and dodecane interact, respectively, with the hydrophilic and hydrophobic moieties in the DES structure, primarily the sulfobetaine, thereby swelling and solvating the entire structure. The extent of the shift of the peak position, and the swelling, depend on concentration of the additive. The solution phase organization and the interaction of polar and nonpolar species as observed here, have the potential to affect the ordering of inorganic or polymeric materials grown in such solvents, paving new avenues for templating applications.

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