Switchable solvents and methods of use thereof
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 composition comprising:
(a) CO 2 from a source other than air; and
(b) a switchable solvent formed by combining:
an amount of at least one R′OH, water, or a combination thereof, wherein R′ is alkyl, alkenyl, alkynyl, aryl, silyl, or siloxyl, and may be linear, branched, or cyclic, and may be substituted or unsubstituted;
with an amount of
a compound of formula (1)
wherein
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 or branched; a substituted or unsubstituted C 3 to C 10 cycloalkyl group; 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) and the corresponding ionic liquid of formula (2) may be a monocyclic or bicyclic ring structure;
wherein the compound of formula (1) reversibly converts to
an ionic liquid of formula (2)
in the presence of the CO 2 ,
wherein R is H or R′ as defined above, and R 1 , R 2 , R 3 , and R 4 are as defined above; and
wherein the amount of the compound of formula (1) is approximately equimolar to or greater than equimolar to the amount of the at least one R′OH, water, or combination thereof.
2. The composition of claim 1 , wherein the CO 2 is gaseous and is present at a pressure of at least 1 atm.
3. The composition of claim 1 , wherein the CO 2 is gaseous and is present at a pressure of greater than 1 atm.
4. The composition of claim 1 , wherein R 1 , R 3 and R 4 are not hydrogen.
5. The composition of claim 1 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
6. The composition of claim 5 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
7. The composition of claim 1 , wherein the ionic liquid of formula (2) is a monocyclic or bicyclic ring structure.
8. The composition of claim 7 , wherein the ionic liquid of formula (2) is protonated 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU H + ”)HOCO 2 − .
9. The composition of claim 1 , wherein the at least one R′OH is a primary or a secondary alcohol.
10. The composition of claim 1 , wherein one or more of R 1 , R 2 , R 3 , and R 4 is substituted with hydroxyl.
11. The composition of claim 1 , wherein R′ is substituted with 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.
12. The composition of claim 1 , wherein one or more of R 1 , R 2 , R 3 , R 4 , and R 6 is independently substituted with 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.
13. The composition of claim 1 , wherein the ionic liquid is [DBUH] + [ROCO 2 ] − where R is R′ and the at least one R′OH comprises 1-propanol, 1-butanol, 1-hexanol, 1-octanol, 2-octanol, 1-decanol, or phenol.
14. The composition of claim 1 , wherein the amount of the compound of formula (1) is approximately equimolar to the amount of the at least one R′OH, water or combination thereof.
15. The composition of claim 1 , wherein the amount of the compound of formula (1) is greater than equimolar to the amount of the at least one R′OH, water or combination thereof.
16. The composition of claim 1 , wherein R 1 , R 2 , R 3 , and R 4 are independently a substituted or unsubstituted C 1 to C 4 alkyl group that is linear or branched.
17. The composition of claim 1 , wherein R is H or alkyl.
18. A composition comprising:
(a) CO 2 from a source other than air; and
(b) a switchable solvent formed by combining:
at least one R′OH, water, or a combination thereof, wherein R′ is alkyl, alkenyl, alkynyl, aryl, silyl, or siloxyl, and may be linear, branched, or cyclic, and may be substituted or unsubstituted;
with a compound of formula (1)
wherein
R 1 , R 2 , R 3 , and R 4 are independently H; a substituted or unsubstituted C 1 to C 4 alkyl group that is linear or branched; a substituted or unsubstituted C n Si m group where n and m are independently a number from 0 to 4 and n+m is a number from 1 to 4; a substituted or unsubstituted C 3 or C 4 cycloalkyl group; 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) and the corresponding ionic liquid of formula (2) may be a monocyclic or bicyclic ring structure;
wherein the compound of formula (1) reversibly converts to an ionic liquid of formula (2)
in the presence of the CO 2 ,
wherein R is H or R′ as defined above, and R 1 , R 2 , R 3 , and R 4 are as defined above.
19. The composition of claim 18 , wherein the CO 2 is gaseous and is present at a pressure of at least 1 atm.
20. The composition of claim 18 , wherein the CO 2 is gaseous and is present at a pressure of greater than 1 atm.
21. The composition of claim 18 , wherein R 1 , R 3 and R 4 are not hydrogen.
22. The composition of claim 18 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
23. The composition of claim 22 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
24. The composition of claim 18 , wherein the ionic liquid of formula (2) is a monocyclic or bicyclic ring structure.
25. The composition of claim 24 , wherein the ionic liquid of formula (2) is protonated 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU H + ”) HOCO 2 − .
26. The composition of claim 18 , wherein the at least one R′OH is a primary or a secondary alcohol.
27. The composition of claim 18 , wherein R′ is substituted with 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.
28. The composition of claim 18 , wherein one or more of R 1 , R 2 , R 3 , R 4 , and R 6 is independently substituted with one or more of heteroaryl, 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, thioester, and alkyl halide; and
substituents for R 6 include 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.
29. The composition of claim 28 , wherein one or more of R 1 , R 2 , R 3 , and R 4 is substituted with hydroxyl.
30. The composition of claim 18 , wherein the ionic liquid is [DBUH] + [ROCO 2 ] − where R is R′ and the at least one R′OH comprises 1-propanol, 1-butanol, 1-hexanol, 1-octanol, 2-octanol, 1-decanol, or phenol.
31. The composition of claim 18 , wherein the compound of formula (1) and the at least one R′OH, water or combination thereof, are present in approximately equimolar amounts.
32. The composition of claim 18 , wherein the compound of formula (1) is present at an amount that is less than equimolar to the amount present of the at least one R′OH, water or combination thereof.
33. The composition of claim 18 , wherein the compound of formula (1) is present at an amount that is more than equimolar to the amount present of the at least one R′OH, water or combination thereof.
34. The composition of claim 18 , wherein R 1 , R 2 , R 3 , and R 4 are independently an unsubstituted C 1 to C 4 alkyl group that is linear or branched.
35. The composition of claim 18 , wherein R is H or alkyl.
36. A composition comprising:
(a) CO 2 from a source other than air; and
(b) a switchable solvent having switchable polarity between a polar form and a nonpolar form, wherein said switchable solvent comprises:
at least one R′OH, water, or a combination thereof, wherein R′ is alkyl, alkenyl, alkynyl, aryl, silyl, or siloxyl, and may be linear, branched, or cyclic, and may be substituted or unsubstituted; and a compound of formula (1)
wherein
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 or branched; a substituted or unsubstituted C 3 to C 10 cycloalkyl group; 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) and the corresponding ionic liquid of formula (2) may be a monocyclic or bicyclic ring structure; and wherein, optionally, one of R 1 , R 2 , R 3 , and R 4 combines with R′ to connect the hydroxyl of the at least one R′OH as part of the compound of formula (1);
wherein the compound of formula (1) reversibly converts to an ionic liquid of formula (2)
in the presence of the CO 2 ,
wherein R is H or R′ as defined above, and R 1 , R 2 , R 3 , and R 4 are as defined above, wherein the polarity of the switchable solvent is switched by the interconversion of the compound of formula (1) and the ionic liquid of formula (2).
37. The composition of claim 36 , wherein the CO 2 is gaseous and is present at a pressure of at least 1 atm.
38. The composition of claim 36 , wherein the CO 2 is gaseous and is present at a pressure of greater than 1 atm.
39. The composition of claim 36 , wherein R 1 , R 3 and R 4 are not hydrogen.
40. The composition of claim 36 , wherein the compound of formula (1) is a monocyclic or bicyclic ring structure.
41. The composition of claim 40 , wherein the compound of formula (1) is 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU”).
42. The composition of claim 36 , wherein the ionic liquid of formula (2) is a monocyclic or bicyclic ring structure.
43. The composition of claim 42 , wherein the ionic liquid of formula (2) is protonated 1,8-diazabicyclo-[5.4.0]-undec-7-ene (“DBU H + ”) HOCO 2 − .
44. The composition of claim 36 , wherein the at least one R′OH is a primary or a secondary alcohol.
45. The composition of claim 36 , wherein R′ is substituted with 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.
46. The composition of claim 36 , wherein one or more of R 1 , R 2 , R 3 , and R 4 is independently substituted with 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.
47. The composition of claim 46 , wherein one of R 1 , R 2 , R 3 , and R 4 combines with R′ to connect the hydroxyl of the at least one R′OH as part of the compound of formula (1).
48. The composition of claim 36 , wherein the ionic liquid is [DBUH] + [ROCO 2 ] − where R is R′ and the at least one R′OH comprises 1-propanol, 1-butanol, 1-hexanol, 1-octanol, 2-octanol, 1-decanol, or phenol.
49. The composition of claim 36 , wherein the compound of formula (1) and the at least one R′OH, water or combination thereof, are present in approximately equimolar amounts.
50. The composition of claim 36 , wherein the compound of formula (1) is present at an amount that is less than equimolar to the amount present of the at least one R′OH, water or combination thereof.
51. The composition of claim 36 , wherein the compound of formula (1) is present at an amount that is more than equimolar to the amount present of the at least one R′OH, water or combination thereof.
52. The composition of claim 36 , wherein R 1 , R 2 , R 3 , and R 4 are independently a substituted or unsubstituted C 1 to C 4 alkyl group that is linear or branched.
53. The composition of claim 36 , wherein R is H or alkyl.