Coupling reaction of carbon dioxide and epoxides efficiently catalyzed by one-component aluminum-salen complex under solvent-free conditions

Journal of Industrial and Engineering Chemistry

Volumn 18, Issue 4, 2012, Pages 1332-1338

  Tian, Dawei ^a   Liu, Binyuan ^a   Zhang, Li ^a   Wang, Xiaoyang ^a   Zhang, Wei ^a   Han, Lina ^b   Park, Dae Won ^b  

^a HEBEI UNIVERSITY OF TECHNOLOGY   (China)

^b Pusan National University   (South Korea)

Author keywords

Bifunctional aluminum salen complex; Carbon dioxide; Cycloaddition; Propylene carbonate; Propylene oxide

Indexed keywords

ALUMINUM-SALEN COMPLEXES; BIFUNCTIONAL; CATALYTIC EFFICIENCIES; CATALYTIC PERFORMANCE; COOPERATIVE EFFECTS; COUPLING REACTION; IMPURITIES IN; LEWIS ACIDIC; LEWIS BASE; METAL CENTERS; NMR SPECTRUM; PHOSPHONIUM SALTS; PROPYLENE CARBONATE; PROPYLENE OXIDE; REACTION VARIABLES; SINGLE-COMPONENT CATALYSTS; SOLVENT FREE CONDITIONS; TERT-BUTYL GROUP;

ALUMINUM; CARBON DIOXIDE; CATALYST ACTIVITY; COMPLEXATION; CYCLOADDITION; ISOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROPYLENE; SYNTHESIS (CHEMICAL);

OPTICAL SENSORS;

EID: 84862828408     PISSN: 1226086X     EISSN: 22345957     Source Type: Journal    
DOI: 10.1016/j.jiec.2012.01.034     Document Type: Article

References (55)

1. Dai W.L., Luo S.L., Yin S.F., Au C.T. Appl. Catal. A: Gen. 2009, 366:2.
2. Sakakura T., Choi J.C., Yasuda H. Chem. Rev. 2007, 107:2365.
3. Xu K. Chem. Rev. 2004, 104:4303.
4. Sakakura T., Kohno K. Chem. Commun. 2009, 1312.
5. Shen Y.M., Duan W.L., Shi M. Adv. Synth. Catal. 2003, 345:337.
6. Shen Y.M., Duan W.L., Shi M., Shen Y.M., Duan W.L., Shi M. Eur. J. Org. Chem. 2004, 14:3080.
7. Barbarini A., Maggi R., Mazzacani A., Mori G., Sartori G., Sartorio R. Tetrahedron Lett. 2003, 44:2931.
8. Jiang J.L., Hua R.M. Synth. Commun. 2006, 36:3141.
9. North M., Pasquale R., Young C. Green Chem. 2010, 12:1514.
10. Sun J., Ren J., Zhang S., Cheng W. Tetrahedron Lett. 2009, 50:423.
11. Yu J.I., Ju H.Y., Kim K.H., Park D.W. Korean J. Chem. Eng. 2010, 27:446.
12. Zhou Y.X., Hu S.Q., Ma X.M., Liang S.G., Jiang T., Han B.X. J. Mol. Catal. A: Chem. 2008, 284:52.
13. Han L., Choi H.J., Choi S.J., Liu B., Park D.W. Green Chem. 2011, 13:1023.
14. Sun J., Zhang S.J., Cheng W.G., Ren J.Y. Tetrahedron Lett. 2008, 49:3588.
15. Jin L.L., Jing H.W., Chang T., Bu X.L., Wang L., Liu Z.L. J. Mol. Catal. A: Chem. 2007, 261:262.
16. Paddock R.L., Hiyama Y.K., Mckay J.M., Nguyen S.T. Tetrahedron Lett. 2004, 45:2023.
17. Man M.L., Lam K.C., Sit W.N., Ng S.M., Zhou Z.Y., Lin Z.Y., Lau C.P. Chem. Eur. J. 2006, 12:1004.
18. Jin L.L., Huang Y.Z., Jing H.W., Chang T., Yan P. Tetrahedron: Asymmetry 2008, 16:1947.
19. Paddock R.L., Nguyen S.T. J. Am. Chem. Soc. 2001, 123:11498.
20. Lu X.B., Liang B., Zhang Y.J., Tian Y.Z., Wang Y.M., Bai C.X., Wang H., Zhang R. J. Am. Chem. Soc. 2004, 126:3732.
21. Jutz F., Grunwaldt J.D., Baiker A. J. Mol. Catal. A: Chem. 2008, 279:94.
22. Lu X.B., Zhang Y.J., Liang B., Li X., Wang H. J. Mol. Catal. A: Chem. 2004, 210:31.
23. Luinstra G.A., Haas G.R., Molnar F., Bernhart V., Eberhardt R., Rieger B. Chem. Eur. J. 2005, 11:6298.
24. Paddock R.L., Nguyen S.T. Chem. Commun. 2004, 1622.
25. Noh E.K., Na S.J., Sujith S., Kim S.W., Lee B.Y. J. Am. Chem. Soc. 2007, 129:8082.
26. Sujith S., Min J.K., Seong J.E., Na S.J., Lee B.Y. Angew. Chem. Int. Ed. 2008, 47:7306.
27. Ren W.M., Zhang X., Liu Y., Li J.F., Wang H., Lu X.B. Macromolecules 2010, 43:1396.
28. Liu B.Y., Gao Y.H., Zhao X., Yan W.D., Wang X.H. J. Polym. Sci. A Polym. Chem. 2010, 48:359.
29. Matin N., Altable M., Filippone S. Angew. Chem. Int. Ed. 2006, 45:1.
30. Chang T., Jing L.L., Jin H.W. ChemCatChem 2009, 1:379.
31. Zhang X., Jia Y.B., Lu X.B., Li B., Wang H., Sun L.C. Tetrahedron Lett. 2008, 49:6589.
32. Miao C.X., Wang J.Q., Wu Y., Du Y., He L.N. ChemSusChem 2008, 1:236.
33. Tan R., Yin D., Yu N., Jin Y., Zhao H., Yin D. J. Catal. 2008, 255:287.
34. Darensbourg D.J., Billodeaux D.R. Inorg. Chem. 2005, 44:1433.
35. Henderson W.A., Streuli C.A. J. Am. Chem. Soc. 1960, 82:5794.
36. Wolff M.O., Alexander K.M., Belder G. Chim. Oggi 2000, 18:29.
37. Bradaric C.J., Downard A., Kennedy C., Robertson A.J., Zhou Y.H. Green Chem. 2003, 5:143.
38. Sesto R.E., Corley C., Robertson A., Wilkes J.S. J. Organomet. Chem. 2005, 690:2536.
39. Minutolo F., Pini D., Petri A., Salvadori P. Tetrahedron: Asymmetry 1996, 7:2293.
40. Larrow J.F., Jacobsen E.N. J. Org. Chem. 1994, 59:1939.
41. Taden I., Kang H.C., Massa W., Okuda J. J. Organomet. Chem. 1997, 540:189.
42. Sugimoto H., Ohtsuka H., Inoue S. J. Polym. Sci. A: Polym. Chem. 2005, 43:4172.
43. Lu X.B., He R., Bai C.X. J. Mol. Catal. A: Chem. 2002, 186:1.
44. Ropson N., Dubois P., Jerome R., Teyssie P. Macromolecules 1993, 26:6378.
45. Dhammani A., Bohra R., Mehrotra R.C. Polyhedron 1998, 17:163.
46. Atwood D.A., Harvey M.J. Chem. Rev. 2001, 101:37.
47. Baleiza C., Garcia H. Chem. Rev. 2006, 106:3987.
48. Melendez J., North M., Pasquale R. Eur. J. Inorg. Chem. 2007, 3323.
49. Ramin M., Jutz F., Grunwaldt J.D., Baiker A. J. Mol. Catal. A: Chem. 2005, 242:32.
50. Holtzclaw H.F., Carlson A.H., Collman J.P. J. Am. Chem. Soc. 1956, 78:1838.
51. Mcdaniel D.H., Brown H.C. J. Org. Chem. 1958, 23:420.
52. Liu B.Y., Li H.Q., Ha C.S., Kim I., Yan W.D. Macromol. Res. 2008, 16:441.
53. Eberhardt R., Allmendinger M., Rieger B. Macromol. Rapid Commun. 2003, 24:194.
54. Darensbourg D.J., Phelps A.L. Inorg. Chem. 2005, 44:4622.
55. Takahashi T., Watahiki T., Kitazume S., Yasuda H., Sakakura T. Chem. Commun. 2006, 1664.