Affiliations 

  • 1 Department of Chemistry, Norwegian University of Science and Technology, Trondheim, Norway
  • 2 Center of Research in Ionic Liquids (CORIL), Universiti Teknologi PETRONAS, Perak, Malaysia
  • 3 Université Grenoble Alpes (UGA), Grenoble, France
  • 4 SINTEF Industry, Sustainable Energy Technology, Trondheim, Norway
Front Chem, 2019;7:625.
PMID: 31620423 DOI: 10.3389/fchem.2019.00625

Abstract

Structurally modified hydroxyl functionalized pyridinium ionic liquids (ILs), liquid at room temperature, were synthesized and characterized. Alkylated N-(2-hydroxyethyl)-pyridinium ILs were prepared from alkylpyridines via corresponding bromide salts by N-alkylation (65-93%) and final anion exchange (75-96%). Pyridinium-alkylation strongly influenced the IL physicochemical and electrochemical properties. Experimental values for the ILs physicochemical properties (density, viscosity, conductivity, and thermal decomposition temperature), were in good agreement with corresponding predicted values obtained by theoretical calculations. The pyridinium ILs have electrochemical window of 3.0-5.4 V and were thermally stable up to 405°C. The IL viscosity and density were measured over a wide temperature range (25-80°C). Pyridine alkyl-substitution strongly affected the partial positive charge on the nitrogen atom of the pyridinium cations, as shown by charge distribution calculations. On-going studies on Mg complexes of the new ILs demonstrate promising properties for high current density electrodeposition of magnesium.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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