Hydroformylation of higher olefin in halogen-free ionic liquids catalyzed by water-soluble rhodium-phosphine complexes

Applied Catalysis A: General

Volumn 328, Issue 1, 2007, Pages 83-87

  Lin, Qi ^a,b   Jiang, Weidong ^b   Fu, Haiyan ^b   Chen, Hua ^b   Li, Xianjun ^b  

^a MINJIANG UNIVERSITY   (China)

^b BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

Author keywords

1 n alkyl 3 methylimidazolium p toluenesulfonate; Hydroformylation; Ionic liquid; Water soluble rhodium phosphine complexes

Indexed keywords

1-N-ALKYL-3-METHYLIMIDAZOLIUM P-TOLUENESULFONATE; CHEMOSELECTIVITY; WATER SOLUBLE RHODIUM PHOSPHINE COMPLEXES;

ALDEHYDES; CHAIN LENGTH; HYDROFORMYLATION; IONIC LIQUIDS; OLEFINS; REACTION RATES; RHODIUM COMPOUNDS;

CATALYST ACTIVITY;

EID: 34447304055     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apcata.2007.05.032     Document Type: Article

References (27)

1. Baker R.T., and Tumas W. Science 284 (1999) 1477
2. Cole-Hamilton D.J. Science 299 (2003) 1702
3. Kuntz E.G. Chemtech. 17 (1987) 570
4. Cornils B., Herrmann W.A., and Eckl R.W. J. Mol. Catal. A: Chem. 116 (1997) 27
5. Herrmann W.A., and Kohlpaintner C.W. Angew. Chem. Int. Ed. Engl. 32 (1993) 1524
6. Cornils B. In: Cornils B., and Hermann W.A. (Eds). Appiled Homogeneous Catalysis with Organometallic Compounds vol. 1 (1996), VCH, Weinheim 577-600
7. Wasserscheid P., and Keim W. Angew. Chem. Int. Ed. 39 (2000) 3772
8. Welton T. Chem. Rev. 99 (1999) 2071
9. Dupont J., Souza R.F., and Suarez P.A.Z. Chem. Rev. 102 (2002) 3667
10. Chauvin Y., Mussmann L., and Olivier H. Angew. Chem. Int. Ed. Engl. 34 (1995) 2698
11. Wasserscheid P., Waffenschmidt H., Machnitzki P., Kottsieper K.W., and Stelzer O. Chem. Commun. (2001) 451
12. Mehnert P., Cook R.A., Dispenziere N.C., and Mozeleski E.J. Polyhedron 23 (2004) 2679
13. Webb P.B., Sellin M.F., Kunene T.E., Williamson S., Slawin A.M.Z., and Cole-Hamilton D.J. J. Am. Chem. Soc. 125 (2003) 15577
14. Chen H., Li X., Li Y., and Liu H. ZL 96 120055.3 (1996)
15. Grushin V.V., and Alper H. Organometallics 12 (1993) 1890
16. McCleverty J.A., and Kilkinson G. Inorg. Synth. 8 (1966) 211
17. Bonati F., and Kilkinson G. J. Chem. Soc. (1964) 3156
18. Giordano G., and Crabtree R.H. Inorg. Synth. 28 (1990) 88
19. Li X., Chen H., Li Y., and Liu H. ZL 96 120056.1 (1996)
20. Suarez P.A.Z., Dullius J.E.L., Einloft S., de Souza R.F., and Dupont J. Polyhedron 15 (1996) 1217
21. Holbrey J.D., and Seddon K.R. J. Chem. Soc. Dalton Trans. (1999) 2133
22. Huddleston J.G., Willauer H.D., Swatloski R.P., Visser A.E., and Rogers R.D. Chem. Commun. (1998) 1765
23. 2O).
24. Casey C.P., Whiteker G.T., Melville M.G., Petrovich L.M., Gavney Jr. J.A., and Powell D.R. J. Am. Chem. Soc. 114 (1992) 5535
25. Chen H., Li Y., Li R., Cheng P., and Li X. J. Mol. Catal. A: Chem. 198 (2003) 1
26. Yuan M., Chen H., Li R., Li Y., and Li X. Catal. Lett. 94 (2004) 15
27. Chen H., Li Y., Chen J., Cheng P., and Li X. Catal. Today 74 (2002) 131