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Triphilic Ionic‐Liquid Mixtures: Fluorinated and Non‐fluorinated Aprotic Ionic‐Liquid Mixtures
Authors:Dr Oldamur Hollóczki  Dr Marina Macchiagodena  Henry Weber  Martin Thomas  Dr Martin Brehm  Prof?Dr Annegret Stark  Dr Olga Russina  Dr Alessandro Triolo  Prof?Dr Barbara Kirchner
Institution:1. Mulliken Center for Theoretical Chemistry, Rheinische Friedrich-Wilhelms-Universit?t Bonn, Bonn, Germany;2. Helmholtz-Zentrum für Umweltforschung Leipzig, Department ?kologische Chemie, Leipzig, Germany;3. SMRI Sugarcane Biorefinery Research Chair, University of KwaZulu-Natal, College of Agriculture, Engineering and Science School of Engineering, Durban, South Africa;4. Department of Chemistry, Sapienza University of Rome, Rome, Italy;5. Laboratorio Liquidi Ionici, Istituto Struttura della Materia, Consiglio Nazionale delle Ricerche, Rome, Italy
Abstract:We present here the possibility of forming triphilic mixtures from alkyl‐ and fluoroalkylimidazolium ionic liquids, thus, macroscopically homogeneous mixtures for which instead of the often observed two domains—polar and nonpolar—three stable microphases are present: polar, lipophilic, and fluorous ones. The fluorinated side chains of the cations indeed self‐associate and form domains that are segregated from those of the polar and alkyl domains. To enable miscibility, despite the generally preferred macroscopic separation between fluorous and alkyl moieties, the importance of strong hydrogen bonding is shown. As the long‐range structure in the alkyl and fluoroalkyl domains is dependent on the composition of the liquid, we propose that the heterogeneous, triphilic structure can be easily tuned by the molar ratio of the components. We believe that further development may allow the design of switchable, smart liquids that change their properties in a predictable way according to their composition or even their environment.
Keywords:ionic liquids  microphases  molecular dynamics  nanosegregation fluorination  simulations microheterogen
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