Brønsted acidic ionic liquid as an efficient and recyclable promoter for hydroesterification of olefins catalyzed by a triphenylphosphine-palladium complex

Catalysis Communications

Volumn 11, Issue 15, 2010, Pages 1200-1204

  Yang, Jing ^a   Zhou, Hancheng ^a   Lu, Xinning ^a   Yuan, Youzhu ^a  

^a XIAMEN UNIVERSITY   (China)

Author keywords

Acidity; Br nsted acidic ionic liquid; Hydroesterification; Triphenylphosphine palladium complex

Indexed keywords

ACIDITY; CATALYSIS; CATALYST SELECTIVITY; CATALYSTS; IONIC LIQUIDS; LIQUIDS; OLEFINS;

ACIDIC IONIC LIQUIDS; CATALYTIC PERFORMANCE; HAMMETT ACIDITY FUNCTION; HIGH CONVERSIONS; HYDROESTERIFICATION; PALLADIUM COMPLEXES; REACTION CONVERSION; TRIPHENYL PHOSPHINES;

PALLADIUM COMPOUNDS;

EID: 77955184180     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2010.05.025     Document Type: Article

References (22)

1. J. Falbe, New Synthesis with Carbon Monoxide, Springer Verlag, Berlin, 1980, p. 243.
2. G. Kiss, Chem. Rev. 101 (2001) 3435-3456.
3. B.R. Sarkar, R.V. Chaudhari, Catal. Surv. Asia 9 (2005) 193-205.
4. A. Seayad, A.A. Kelkar, L. Toniolo, R.V. Chaudhari, J. Mol. Catal. A: Chem. 151 (2000) 47-59.
5. G. Cavinato, L. Toniolo, A. Vavasori, J. Mol. Catal. A: Chem. 219 (2004) 233-240.
6. H. Ooka, T. Inoue, S. Itsuno, M. Tanaka, Chem. Commun. 48 (2005) 1173-1175.
7. A.C. Ferreira, R. Crous, L. Bennie, A.M.M. Meij, K. Blann, B.C.B. Bezuidenhoudt, D.A. Young, M.J. Green, A. Roodt, Angew. Chem. Int. Ed. 46 (2007) 2273-2275.
8. D.B.G. Williams, M.L. Shaw, M.J. Green, C.W. Holzapfel, Angew. Chem. Int. Ed. 47 (2008) 560-563.
9. J. Yang, Y.Z. Yuan, Catal. Lett. 131 (2009) 643-648.
10. G. Rangits, L. Kollár, J. Mol. Catal. A: Chem. 242 (2005) 156-160.
11. G. Rangits, L. Kollár, J. Mol. Catal. A: Chem. 246 (2006) 59-64.
12. M.A. Klingshirn, R.D. Rogers, K.H. Shaughnessy, J. Organomet. Chem. 690 (2005) 3620-3626.
13. A. Balázs, C. Benedek, S. Törös, J. Mol. Catal. A: Chem. 244 (2006) 105-109.
14. Z.S. Qureshi, K.M. Deshmukh, M.D. Bhor, B.M. Bhanage, Catal. Commun. 10 (2009) 833-837.
15. H.B. Xing, T. Wang, Z.H. Zhou, Y.Y. Dai, Ind. Eng. Chem. Res. 44 (2005) 4147-4150.
16. H.B. Xing, T. Wang, Z.H. Zhou, Y.Y. Dai, J. Mol. Catal. A: Chem. 264 (2007) 53-59.
17. Y.W. Zhao, J.X. Long, F.G. Deng, X.F. Liu, Z. Li, C.G. Xia, J.J. Peng, Catal. Commun. 10 (2009) 732-736.
18. H.L. Li, S.T. Yu, F.S. Liu, C.X. Xie, L. Li, Catal. Commun. 8 (2007) 1759-1762.
19. C. Thomazeau, H. Olivier-Bourbigou, L. Magna, S. Luts, B. Gilbert, J. Am. Chem. Soc. 125 (2003) 5264-5265.
20. Z.Y. Du, Z.P. Li, S. Guo, J. Zhang, L.Y. Zhu, Y.Q. Deng, J. Phys. Chem. B. 109 (2005) 19542-19546.
21. A. Beyaz, W.S. Oh, V.P. Reddy, Colloids Surf. B Biointerfaces 35 (2004) 119.
22. C.A. Ohlin, P.J. Dyson, G. Laurenczy, Chem. Commun. 9 (2004) 1070-1071.