4.6 Article

Synthesis and characterization of the thermodynamic and electrochemical properties of tetra-alkyl phosphonium oxalate ionic liquids

Journal

RSC ADVANCES
Volume 4, Issue 29, Pages 14840-14846

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra01467g

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Funding

  1. Los Alamos Laboratory Directed Research and Development Program
  2. G. T. Seaborg Institute for Transactinium Science at Los Alamos National Laboratory

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Ionic liquids (ILs) are attractive alternatives to water, high temperature molten salts or conventional organic solvents for electrodeposition of technologically important metals. Designing ILs containing functional groups specifically targeted to interact with or even chelate metals, such as carboxylate, may increase the metal solubility and affect thermodynamic and electrochemical properties. This paper reports the synthesis and characterization of three ionic liquids comprised of one or two tetra-alkyl phosphonium cations paired with a hydrogen oxalate or oxalate anion, with the general formula [(P-RRRR')(x)][C2O4H2-x], R = 4,6 and R' = 4, 14. These compounds were characterized by H-1, C-13, P-31 NMR, and Raman spectroscopy. Electrochemical windows, electrical conductivities, densities and viscosities were also determined experimentally. Thermal gravimetric analysis (TGA) revealed decomposition temperatures above 200 degrees C and differential scanning calorimetry (DSC) analysis revealed that the two [(P-66614)(x)][C2O4H2-x] salts have similar glass transition temperatures while [(P-4444)(2)][C2O4] has a melting point above room temperature. Raman and powder X-ray diffraction spectroscopy confirm that Nd2O3 dissolves and complexes with [P-66614][C2O4].

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