2008
DOI: 10.1021/cm801169c
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Carbon Dioxide and Molecular Nitrogen as Switches between Ionic and Uncharged Room-Temperature Liquids Comprised of Amidines and Chiral Amino Alcohols

Abstract: The properties of reversible, room-temperature, chiral, ionic liquids (L-A-C) are reported. They are easily prepared by passing CO2 gas through equimolar mixtures of a simple amidine (L) and a chiral amino alcohol (A), L/A, derived from a naturally occurring amino acid, and they can be returned to their L/A states by passing a displacing gas, N2, through the ionic liquid; the process of passing from uncharged to charged states can be repeated several times without discernible degradation of each phase. All of … Show more

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Cited by 76 publications
(50 citation statements)
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“…2) [17]. Then, the high-polarity solvent can revert back to its non-ionic form by the removal of CO 2 from solution [18]. The removal of CO 2 is achieved by heating the solution below its boiling point or by sweeping with an inert gas such as nitrogen.…”
Section: Co 2 Binding Organic Liquids (Co 2 Bols)mentioning
confidence: 99%
“…2) [17]. Then, the high-polarity solvent can revert back to its non-ionic form by the removal of CO 2 from solution [18]. The removal of CO 2 is achieved by heating the solution below its boiling point or by sweeping with an inert gas such as nitrogen.…”
Section: Co 2 Binding Organic Liquids (Co 2 Bols)mentioning
confidence: 99%
“…These were obtained by bubbling CO 2 gas through a 1:1 mixture of an amidine (N 0 -alkyl-N,N-dimethylacetamidine) and an amino acid ester 44 or aminoalcohol 45 (obtained through reduction of an amino acid with lithium aluminum hydride). The synthetic route is shown in Figure 2.…”
Section: Synthesis Of Chiral Ionic Liquids Cils Derived From Amino Acidsmentioning
confidence: 99%
“…Then, CO 2 is removed from CO 2 BOLs below the boiling point of the mixture by simple heating or sweeping with an inert gas such as nitrogen. They have tunable physicochemical properties; the solvent reverts back to its less-polar non-ionic form and is ready for future CO 2 uptake (Tao Yu et al 2008). The main advantages of these systems are high CO 2 binding capacities, low heat capacities and lower energy requirement for regeneration as compared to aqueous alkanolamine solutions (Mathias et al 2013).…”
Section: Introductionmentioning
confidence: 99%