High stability diionic liquid salts
The present invention relates to diionic liquid salts of dicationic or dianionic molecules, as well as solvents comprising diionic liquids and the use of diionic liquids as the stationary phase in a gas chromatographic column.
1. A method of separating one chemical from a mixture of chemicals comprising the steps of: providing a mixture of at least one first and at least one second chemical, exposing said mixture to at least one
capillary column and at least one diionic liquid salt adsorbed, absorbed or immobilized thereon, wherein the diionic liquid salt comprises at least one di-cation of the formula:
A-B-A′
and at least one counter anion; wherein:
A and A′ are mono-cationic groups independently selected from the group consisting of optionally substituted imidazolium, and pyrrolidinium; wherein
when A and A′ are both substituted imidazolium, at least one of A and A′ is substituted with a group that facilitates cross-linking and/or immobilization; and
bridging group, B, is an optionally substituted C 2 -C 40 hydrocarbon backbone, wherein the hydrocarbon backbone optionally contains, in addition to carbon and hydrogen atoms, at least one heteroatom selected from the group consisting of nitrogen, oxygen, sulfur and/or silicon atom;
and retaining at least a portion of said first chemical on said solid support capillary column for some period of time.
2. The method of claim 1 , further comprising at least one monoionic liquid mixed with said diionic liquid salt and wherein said mixture is immobilized on said solid support.
3. The method of claim 1 , wherein said mixture is passed through said column such that elution of said first chemical is prevented or delayed.
4. The method of claim 1 , wherein said mixture is carried in a gaseous mobile phase.
5. The method of claim 1 , wherein said solid support is attached to a microsyringe having a hollow needle defining an inner space, said needle being disposed at an end of a barrel and a plunger disposed within said barrel, said solid support being attached to said microsyringe such that it may be retracted into said inner space of said needle when said plunger is retracted from said barrel and exposed from within said needle when said plunger is inserted into said barrel, exposing said solid support from within said needle into said mixture, and retracting said solid support from said mixture, wherein it includes at lease some amount of said first chemical.
6. The method of claim 1 , wherein said capillary column is useful in gas chromatography.
7. The method of claim 1 , wherein said capillary column further comprises a syringe having a hollow needle defining an inner space, said needle being disposed at an end of a barrel and a plunger disposed within said barrel, a solid support being attached to said syringe such that it may be retracted into said inner space of said needle when said plunger is retracted from said barrel and exposed from within said needle when said plunger is inserted into said barrel.
8. The method of claim 1 , wherein said diionic liquid salt is immobilized on said capillary column and wherein said diionic liquid salt includes at least one unsaturated group which can facilitate cross-linking or immobilization.
9. The method of claim 7 , wherein said syringe is a microsyringe.
10. The method of claim 1 , wherein the diionic liquid salt has a solid/liquid transition temperature of about 100° C. or less.
11. The method of claim 1 , wherein the diionic liquid salt has a solid/liquid transition temperature of about 25° C. or less.
12. The method of claim 1 , wherein the bridging group, B, has a length about equivalent to a C 3 -C 30 carbon chain.
13. The method of claim 1 , wherein the bridging group, B, contains at least one unsaturated group which can facilitate cross-linking or immobilization.
14. The method of claim 1 , wherein the bridging group, B, contains at least one heteroatom selected from the group consisting of nitrogen, oxygen, sulfur, and/or silicon.
15. The method of claim 1 , wherein A and A′ are both substituted imidazolium and, at least one of A and A′ is substituted with a group that facilitates cross-linking and/or immobilization.
16. The method of claim 1 , wherein the at least one counter anion is a diionic counter anion.
17. The method of claim 16 , wherein the diionic counter anion is selected from the group consisting of carboxylate, sulfate and sulfonate.
18. The method of claim 1 , wherein the diionic liquid salt comprises two mono-ionic counter anions.
19. The method of claim 18 , wherein the two mono-ionic counter anions are independently selected from the group consisting of Br − , mono-sulfonate, mono-sulphate, NTf 2 − , BF 4 − , trifilate and PF 6 − .
20. The method of claim 1 , wherein A and A′ are pyrrolidinium.
21. The method of claim 1 , wherein the diionic liquid salt comprises,
wherein n is 3 to 30.
22. The method of claim 1 , wherein the diionic liquid salt comprises,
wherein n is 3 to 30.
23. The method of claim 1 , wherein the diionic liquid salt is selected from the group consisting of
wherein n is 3 to 30.
24. The method of claim 23 , wherein the at least one di-cation is selected from the group consisting of:
wherein n is 6, 9, 10, 11, or 12; and
wherein n is 6.
25. The method of claim 21 , wherein the at least one di-cation is of the formula:
wherein n is 3 or 9.
26. The method of claim 22 , wherein the at least one di-cation is of the formula:
wherein n is 9.