Preparation of 1?Butyl?3?Methyl Imidazolium?Based Room Temperature Ionic Liquids
Dupont, Jairton, et al.
Organic Syntheses, 236-236 (2003)
ZnS nanoparticle synthesis in 1-butyl-3-methylimidazolium tetrafluoroborate by simple heating.
Kareem TA and Kaliani AA.
Arabian Journal of Chemistry (2015)
Solubility of carbon dioxide, ethane, methane, oxygen, nitrogen, hydrogen, argon, and carbon monoxide in 1-butyl-3-methylimidazolium tetrafluoroborate between temperatures 283K and 343K and at pressures close to atmospheric
Jacquemin, Johan, et al.
The Journal of Chemical Thermodynamics, 38.4, 490-502 (2006)
Ionic liquid 1-butyl-3-methylimidazolium bromide as a promoter for the formation and extraction capability of poly (ethylene glycol)-potassium citrate aqueous biphasic system at T= 298.15 K
Hamzehzadeh, Sholeh, and Maryam Vasiresh
Fluid Phase Equilibria, 382, 80-88 (2014)
Prussian blue/1-butyl-3-methylimidazolium tetra?uoroborate?Graphite felt electrodes for efficient electrocatalytic determination of nitrite
Wang, Lei, et al.
Sensors and Actuators B, Chemical, 214, 70-75 (2015)
Ionic Liquids have been thoroughly investigated as solvents in most types of catalytic reactions. Their merit lies in the ease with which their physical–chemical properties can be tuned by varying either the anion, the cation, or its substitution pattern.
