ZnBr2/DMF as simple and highly active Lewis acid-base catalysts for the cycloaddition of CO2 to propylene oxide

Journal of CO2 Utilization

Volumn 6, Issue , 2014, Pages 75-79

  Zhong, Shifa ^a   Liang, Lin ^a   Liu, Bo ^a   Sun, Jianmin ^a  

^a HARBIN INSTITUTE OF TECHNOLOGY   (China)

Author keywords

Acid base catalysts; DMF; Propylene carbonate

Indexed keywords

CATALYST SELECTIVITY; INDUSTRIAL APPLICATIONS; PROPYLENE;

ACID-BASE CATALYSTS; CATALYTIC MECHANISMS; CYCLIC CARBONATES; DMF; LEWIS ACID-BASE; LEWIS ACIDS AND BASIS; PROPYLENE CARBONATE;

CARBON DIOXIDE;

EID: 84900491521     PISSN: 22129820     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcou.2014.02.004     Document Type: Article

References (31)

1. M. Aresta Carbon Dioxide as Chemical Feedstock 2010 Wiley-VCH Weinheim
2. R. Martin, and A.W. Kleij ChemSusChem 4 2011 1259 1263
3. T. Sakakura, and K. Kohno Chem. Commun. 11 2009 1312 1330
4. M. North, R. Pasquale, and C. Young Green Chem. 12 2010 1514 1539
5. C. Bruckmeier, B. Rieger, W.A. Herrmann, and F.E. Kühn Angew. Chem. Int. Ed. 50 2011 8510 8537
6. B. Schäffner, F. Schäffner, S.P. Verevkin, and A. Börner Chem. Rev. 110 2010 4554 4581
7. A.A.G. Shaikh, and S. Sivaram Chem. Rev. 96 1996 951 976
8. J.H. Clements Ind. Eng. Chem. Res. 42 2003 663 674
9. Y. Du, F. Cai, D.L. Kong, and L.N. He Green Chem. 7 2005 518 523
10. B.M. Bhanage, S.I. Fujita, Y. Ikushima, and M. Arai Appl. Catal. A: Gen. 219 2001 259 266
11. N. Kihara, N. Hara, and T. Endo J. Org. Chem. 58 1993 6198 6202
12. H.S. Kim, J.J. Kim, B.G. Lee, O.S. Jung, H.G. Jang, and S.O. Kang Angew. Chem. Int. Ed. 39 2000 4096 4098
13. R.L. Paddock, and S.T. Nguyen J. Am. Chem. Soc. 123 2001 11498 11499
14. A. Sibaouih, P. Ryan, K.V. Axenov, M.R. Sundberg, M. Leskelä, and T. Repo J. Mol. Catal. A: Chem. 312 2009 87 91
15. F. Li, C. Xia, L. Xu, W. Sun, and G. Chen Chem. Commun. 16 2003 2042 2043
16. J.M. Sun, S.-I. Fujita, F.Y. Zhao, and M. Arai Appl. Catal. A: Gen. 287 2005 221 226
17. T. Yano, H. Matsui, T. Koike, H. Ishiguro, H. Fujihara, M. Yoshihara, and T. Maeshima Chem. Commun. 12 1997 1129 1130
18. K. Yamaguchi, K. Ebitani, T. Yoshida, H. Yoshida, and K. Kaneda J. Am. Chem. Soc. 121 1999 4526 4527
19. H. Kawanami, and Y. Ikushima Chem. Commun. 21 2000 2089 2090
20. Z.Z. Yang, L.N. He, S.Y. Peng, and A.H. Liu Green Chem. 12 2010 1850 1854
21. M. North, and R. Pasquale Angew. Chem. Int. Ed. 48 2009 1 4
22. F. Li, L. Xiao, C. Xia, and B. Hu Tetrahedron Lett. 45 2004 8307 8310
23. T.Y. Shi, J.Q. Wang, J. Sun, M.H. Wang, W.G. Cheng, and S.J. Zhang RSC Adv. 3 2013 3726 3732
24. J.Q. Wang, X.D. Yue, F. Cai, and L.N. He Catal. Commun. 8 2007 167 172
25. F. Jutz, J.D. Grunwaldt, and A. Baiker J. Mol. Catal. A: Chem. 279 2008 94 103
26. W.L. Dai, B. Jin, S.L. Luo, X.B. Luo, X.M. Tu, and C.T. Au J. Mol. Catal. A: Chem. 378 2013 326 332
27. S.R. Jagtap, V.P. Raje, S.D. Samant, and B.M. Bhanage J. Mol. Catal. A: Chem. 266 2007 69 74
28. R.A. Shiels, and C.W. Jones J. Mol. Catal. A: Chem. 261 2007 160 166
29. H.S. Kim, J.Y. Bae, J.S. Lee, O.-S. Kwon, P. Jelliarko, S.D. Lee, and S.-H. Lee J. Catal. 232 2005 80 84
30. M. Ramin, J.-D. Grunwaldt, and A. Baiker J. Catal. 234 2005 256 267
31. J. Sun, L. Wang, S. Zhang, Z. Li, X. Zhang, W. Dai, and R. Mori J. Mol. Catal. A: Chem. 256 2006 295 300