Switchable solvents and methods of use thereof
View Patent ↗A solvent that reversibly converts from a nonionic liquid mixture to an ionic liquid upon contact with a selected trigger, e.g., contact with CO 2 , is described. In preferred embodiments, the ionic solvent is readily converted back to the nonionic liquid mixture. The nonionic liquid mixture includes an amidine or guanidine or both, and water, alcohol, or a combination thereof. Single component amine solvents that reversibly convert between ionic and non-ionic states are also described. Some embodiments require increased pressure to convert; others convert at 1 atmosphere.
1. A method for separating a nonpolar liquid from a mixture, comprising:
providing a mixture comprising a nonpolar liquid, an alcohol, a compound of formula (1), and CO 2 ,
where the compound of formula (1) is:
where R 1 , R 2 , R 3 , and R 4 are independently H; a substituted or unsubstituted C 1 to C 10 alkyl group that is linear, branched, or cyclic; a substituted or unsubstituted C n Si m group where n and m are independently a number from 0 to 10 and n+m is a number from 1 to 10; a substituted or unsubstituted aryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; or a substituted or unsubstituted heteroaryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; R 6 is a substituted or unsubstituted alkyl, aryl, heteroaryl, or alkoxy moiety; and wherein the compound of formula (1) may be a monocyclic or bicyclic ring structure;
converting the alcohol, the compound of formula (1), and the CO 2 into an ionic liquid, wherein the nonpolar liquid is miscible with the alcohol and compound of formula (1), but is immiscible with the ionic liquid, and wherein the nonpolar liquid is not reactive with the compound of formula (1) in the presence of the CO 2 ; and
separating the ionic liquid and the nonpolar liquid to isolate the nonpolar liquid.
2. A method for separating a nonpolar solute from a mixture, comprising:
providing a mixture comprising a nonpolar solute, water, a compound of formula (1), and CO 2 , COS, CS 2 or a combination thereof,
wherein the compound of formula (1) is:
where R 1 , R 2 , R 3 , and R 4 are independently H; a substituted or unsubstituted C 1 to C 10 alkyl group that is linear, branched, or cyclic; a substituted or unsubstituted C n Si m group where n and m are independently a number from 0 to 10 and n+m is a number from 1 to 10; a substituted or unsubstituted aryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; or a substituted or unsubstituted heteroaryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; R 6 is a substituted or unsubstituted alkyl, aryl, heteroaryl, or alkoxy moiety; and wherein the compound of formula (1) may be a monocyclic or bicyclic ring structure;
converting the water, the compound of formula (1), and the CO 2 , COS, CS 2 or combination thereof into an ionic liquid, wherein the nonpolar solute is miscible with the water and compound of formula (1), but is immiscible with the ionic liquid, and wherein the nonpolar solute is not reactive with the compound of formula (1) in the presence of the CO 2 , COS, or CS 2 ; and
separating the ionic liquid and the nonpolar solute to isolate the nonpolar solute.
3. The method of claim 1 , wherein the compound of formula (1) is added to a mixture of the nonpolar liquid and alcohol.
4. The method of claim 1 , wherein the CO 2 is added to a mixture of the nonpolar liquid and alcohol.
5. The method of claim 1 , wherein the mixture including the compound of formula (1) comprises an amount of amidine that is less than equimolar to the amount of alcohol so that after forming the ionic liquid, some alcohol remains in non-ionic form.
6. The method of claim 1 , wherein the mixture including the compound of formula (1) comprises an amount of amidine that is greater than equimolar to the amount of alcohol so that after forming the ionic liquid, some amidine remains in non-ionic form.
7. The method of claim 1 , wherein the alcohol is ROH, where R is alkyl, alkenyl, alkynyl, aryl, silyl, or siloxyl, and may be linear, branched, or cyclic, and may be substituted or unsubstituted.
8. The method of claim 7 , wherein substituent includes one or more of alkyl, alkenyl, alkynyl, aryl, aryl halide, heteroaryl, cyclyl, Si(alkyl) 3 , Si(alkoxy) 3 , halo, alkoxyl, amino, amide, hydroxyl, thioether, alkylcarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carbonate, alkoxycarbonyl, aminocarbonyl, alkylthiocarbonyl, phosphate, phosphate ester, phosphonato, phosphinato, cyano, acylamino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, dithiocarboxylate, sulfate, sulfato, sulfamoyl, sulfonamide, nitro, nitrile, azido, heterocyclyl, ether, ester, silicon-containing moieties, thioester, and alkyl halide.
9. The method of claim 1 , wherein the alcohol is a primary or a secondary alcohol.
10. The method of claim 1 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by heating the ionic liquid.
11. The method of claim 1 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by contacting the ionic liquid with a nonreactive gas that contains insufficient CO 2 , COS or CS 2 to sustain the ionic liquid in its ionic form.
12. The method of claim 1 , wherein the compound of formula (1) is 1,8 -diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
13. The method of claim 1 , wherein the ionic liquid is [DBUH] +[ROCO 2 ] − where ROH is 1-propanol, 1-butanol, 1-hexanol, 1-octanol, 2-octanol, 1-decanol, or phenol.
14. The method of claim 1 , wherein the nonpolar liquid is a medicinal compound, organic compound, intermediate compound, mineral, synthetic reagent, oil, sugar, food, flavorant, fragrance, dye, pesticide, fungicide, fuel, or spice.
15. The method of claim 14 , wherein the nonpolar liquid is a fuel.
16. A method for separating a nonpolar solute from a mixture, comprising:
providing a mixture comprising a nonpolar solute, an alcohol, a compound of formula (1), and CO 2 , COS, CS 2 or a combination thereof,
where the compound of formula (1) is:
where R 1 , R 2 , R 3 , and R 4 are independently H; a substituted or unsubstituted C 1 to C 10 alkyl group that is linear, branched, or cyclic; a substituted or unsubstituted C n Si m group where n and m are independently a number from 0 to 10 and n+m is a number from 1 to 10; a substituted or unsubstituted aryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; or a substituted or unsubstituted heteroaryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; R 6 is a substituted or unsubstituted alkyl, aryl, heteroaryl, or alkoxy moiety; and
wherein the compound of formula (1) may be a monocyclic or bicyclic ring structure;
converting the alcohol, the compound of formula (1), and the CO 2 , COS, CS 2 or combination thereof into an ionic liquid, wherein the nonpolar solute is miscible with the alcohol and compound of formula (1), but is immiscible with the ionic liquid, and wherein the nonpolar solute is not reactive with the compound of formula (1) in the presence of the CO 2 , COS, or CS 2 ; and
separating the ionic liquid and the nonpolar solute to isolate the nonpolar solute.
17. The method of claim 16 , wherein the nonpolar solute is a medicinal compound, organic compound, intermediate compound, mineral, synthetic reagent, oil, sugar, food, flavorant, fragrance, dye, pesticide, fungicide, fuel, or spice.
18. The method of claim 17 , wherein the nonpolar solute is a fuel.
19. The method of claim 16 , wherein the mixture is a composition comprising:
soil;
clothes;
rock;
water;
equipment;
biological material comprising wood, pulp, paper, beans, seeds, meat, fat, bark, grass, crops, fur, natural fibers, cornstalks or oils; or
manufactured material comprising machined parts, molded parts, extruded material, chemical products, refined oils, refined fuels, fabrics, fibers, or sheets.
20. The method of claim 19 , wherein the mixture is a composition comprising refined oils or refined fuels.
21. The method of claim 1 , wherein the mixture further comprises a conventional solvent.
22. The method of claim 21 , wherein the conventional solvent is tetrahydrofuran or toluene.
23. A method for separating a nonpolar liquid from a mixture, comprising:
providing a mixture comprising a nonpolar liquid, an alcohol, a compound of formula (1), and CO 2 , COS, CS 2 or a combination thereof,
wherein the compound of formula (1) is:
where R 1 , R 2 , R 3 , and R 4 are independently H; a substituted or unsubstituted C 1 to C 10 alkyl group that is linear, branched, or cyclic; a substituted or unsubstituted C n Si m group where n and m are independently a number from 0 to 10 and n+m is a number from 1 to 10; a substituted or unsubstituted aryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; or a substituted or unsubstituted heteroaryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; R 6 is a substituted or unsubstituted alkyl, aryl, heteroaryl, or alkoxy moiety; and wherein the compound of formula (1) may be a monocyclic or bicyclic ring structure;
converting the alcohol, the compound of formula (1), and the CO 2 , COS, or CS 2 or combination thereof into an ionic liquid, wherein the nonpolar liquid is miscible with the alcohol and compound of formula (1), but is immiscible with the ionic liquid, and wherein the nonpolar liquid is not reactive with the compound of formula (1) in the presence of the CO 2 , COS, or CS 2 ; and
separating the ionic liquid and the nonpolar liquid to isolate the nonpolar liquid.
24. The method of claim 23 , wherein the nonpolar liquid is an oil or a fuel.
25. The method of claim 1 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
26. The method of claim 25 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
27. The method of claim 16 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
28. The method of claim 27 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
29. The method of claim 23 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
30. The method of claim 29 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
31. The method of claim 2 , wherein the compound of formula (1) is added to a mixture of water and the nonpolar liquid.
32. A method for separating a nonpolar solute from a mixture, comprising:
providing a mixture comprising a nonpolar solute, a combination of alcohol and water, a compound of formula (1), and CO 2 , COS, or CS 2 or a combination thereof,
wherein the compound of formula (1) is:
where R 1 , R 2 , R 3 , and R 4 are independently H; a substituted or unsubstituted C 1 to C 10 alkyl group that is linear, branched, or cyclic; a substituted or unsubstituted C n Si m group where n and m are independently a number from 0 to 10 and n+m is a number from 1 to 10; a substituted or unsubstituted aryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; or a substituted or unsubstituted heteroaryl group optionally containing one or more {—Si(R 6 ) 2 —O—} units; R 6 is a substituted or unsubstituted alkyl, aryl, heteroaryl, or alkoxy moiety; and wherein the compound of formula (1) may be a monocyclic or bicyclic ring structure;
converting the water, the alcohol, the compound of formula (1), and the CO 2 , COS, CS 2 or combination thereof into an ionic liquid, wherein the nonpolar solute is miscible with the water, alcohol and compound of formula (1), but is immiscible with the ionic liquid, and wherein the nonpolar solute is not reactive with the compound of formula (1) in the presence of the CO 2 , COS, or CS 2 ; and
separating the ionic liquid and the nonpolar solute to isolate the nonpolar solute.
33. The method of claim 32 , wherein substituent includes one or more of alkyl, alkenyl, alkynyl, aryl, aryl halide, heteroaryl, cyclyl, Si(alkyl) 3 , Si(alkoxy) 3 , halo, alkoxyl, amino, amide, hydroxyl, thioether, alkylcarbonyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carbonate, alkoxycarbonyl, aminocarbonyl, alkylthiocarbonyl, phosphate, phosphate ester, phosphonato, phosphinato, cyano, acylamino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, dithiocarboxylate, sulfate, sulfato, sulfamoyl, sulfonamide, nitro, nitrile, azido, heterocyclyl, ether, ester, silicon-containing moieties, thioester, and alkyl halide.
34. The method of claim 32 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by heating the ionic liquid.
35. The method of claim 32 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by contacting the ionic liquid with a nonreactive gas that contains insufficient CO 2 , COS or CS 2 to sustain the ionic liquid in its ionic form.
36. The method of claim 1 , wherein the alcohol is added to a mixture comprising compound of formula (1) and the nonpolar liquid.
37. The method of claim 2 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
38. The method of claim 37 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
39. The method of claim 32 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
40. The method of claim 39 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
41. The method of claim 16 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by heating the ionic liquid.
42. The method of claim 16 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by contacting the ionic liquid with a nonreactive gas that contains insufficient CO 2 , COS or CS 2 to sustain the ionic liquid in its ionic form.
43. The method of claim 23 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by heating the ionic liquid.
44. The method of claim 23 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by contacting the ionic liquid with a nonreactive gas that contains insufficient CO 2 , COS or CS 2 to sustain the ionic liquid in its ionic form.
45. The method of claim 2 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by heating the ionic liquid.
46. The method of claim 2 , wherein the ionic liquid can be converted to a mixture comprising the compound of formula (1) by contacting the ionic liquid with a nonreactive gas that contains insufficient CO 2 , COS or CS 2 to sustain the ionic liquid in its ionic form.