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Synthesis of Triethylamine‐Bridged Basic Tricationic Ionic Liquids and Evaluation of Their Catalytic Efficiencies for Preparation of Arylidene or Alkylidenemalononitrile
Author(s) -
Gogoi Pinky,
Boruah Kabita,
Borah Ruli
Publication year - 2018
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201801719
Subject(s) - ionic liquid , malononitrile , triethylamine , pyridinium , knoevenagel condensation , catalysis , thermogravimetric analysis , benzaldehyde , chemistry , hydroxide , organic chemistry , inorganic chemistry
Two series of basic triethylamine bridged pyridinium/imidazolium tricationic ionic liquids were synthesized as viscous liquids by ion‐pairing with hydroxide, acetate and imidazolide as basic anions. The characterization of tricationic ionic liquids was done using 1 H and 13 C NMR, FT‐IR, Thermogravimetric analysis (TGA), Hammett basicity EI‐MS and elemental analysis techniques. Thermal stabilities were found within the range of 100–150 °C for these ionic liquids. They acted as efficient recyclable homogeneous catalysts for the representative Knoevenagel condensation of benzaldehyde and malononitrile at room temperature stirring in neat condition for 10–20 min. The catalytic activity of these ILs was found to be slightly different from each other for the model reaction and did not follow the same sequence of their measured Hammett basicity value.