Fluoroalkyl-functional imidazoles and imidazolium–based ionic liquids prepared via thiol-ene/yne click chemistry

Abstract

Abstract A fluorinated thiol was systematically investigated against a diverse set of –ene- and –yne-bearing imidazole and imidazolium substrates in the pursuit of new cation-fluorinated, omniphobic (hydrophobic and oleophobic) ionic liquids for aerospace applications. Compounds were prepared using UV-initiated click chemistry at quantitative conversion and purified with relative ease. Seven ionic liquids were synthesized and have isolated yields ranging from 74% to >99%. Five of the new cation-fluorinated ionic liquids are hydrophobic and two are liquids at room temperature. In addition to hydrophobicity, the seven ionic liquids’ solubilities were qualitatively examined across a wide spectrum of conventional organic solvents. Of note, the majority of the prepared ionic liquids are insoluble in water and hexanes yet soluble in methanol, acetone, acetonitrile, and dichloromethane. In addition to intriguing solubility properties, the ionic liquids in this study have high densities without the incorporation of heavy atoms, ranging from 1.596 to 1.924\xa0g\xa0cm−3. The fluorinated salts also show good short-term thermal stability in air, with decomposition temperatures ranging from 215\xa0°C to 320\xa0°C. Other relevant characterization methods include spectroscopy, thermal analysis, and physical property measurements where appropriate. The X-ray crystal structure of a divalent, cation-fluorinated ionic liquid from this study was also obtained and shows unique fluorous domains in the extended structure, providing valuable insight into the materials’ physical properties. This work highlights a family of compounds moving towards omniphobic ionic liquids yielding potential possibilities for future applications.