Highly porous chitosan microspheres supported palladium catalyst for coupling reactions in organic and aqueous solutions

Journal of Organometallic Chemistry

Volumn 704, Issue , 2012, Pages 29-37

  Zeng, Minfeng ^a   Zhang, Xin ^a   Shao, Linjun ^a   Qi, Chenze ^a   Zhang, Xian Man ^a  

^a SHAOXING UNIVERSITY   (China)

Author keywords

Chitosan; Coupling reaction; Palladium catalyst; Porous microspheres

Indexed keywords

AMINO FUNCTIONAL GROUP; AROMATIC HALIDE; CHITOSAN MICROSPHERES; COUPLING REACTION; CROSS-COUPLINGS; CROSSLINKING CHITOSAN; HECK REACTIONS; HETEROGENEOUS CATALYST; HIGH ACTIVITY; HIGH SPECIFIC SURFACE AREA; HOMOCOUPLING; LARGE SIZES; MICROSPHERE STRUCTURE; PALLADIUM CATALYST; POROUS MICROSPHERES; POROUS STRUCTURES; REACTION MIXTURE; SELECTIVE DISSOLUTION; SUPPORTED PALLADIUM; SUPPORTED PALLADIUM CATALYSTS; SURFACE HYDROXYL;

AROMATIC COMPOUNDS; CHEMICAL REACTIONS; CHITOSAN; GLYCOLS; MICROSPHERES; RECYCLING; SOLUTIONS;

CATALYST SELECTIVITY;

EID: 84862784797     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2012.01.003     Document Type: Article

References (36)

1. J. Tsuji Palladium reagents and catalysts second ed. 2004 Wiley New York
2. D.J. Cole-Hamilton Science 299 2003 1702 1706
3. C.E. Garrett, and K. Prasad Adv. Synth. Catal. 346 2004 889 900
4. P. Barbaro, and F. Liguori Chem. Rev. 109 2009 515 529
5. S. Bhaduri, and D. Mukesh Homogenous catalysis: mechanism and industrial applications 2000 Wiley New York 1-8
6. M.F. Zeng, Y.J. Du, C.Z. Qi, S.F. Zuo, X.D. Li, L.J. Shao, and X.-M. Zhang Green Chem. 13 2011 350 356
7. N.V. Kramareva, A.Y. Stakheev, O.P. Tkachenko, K.V. Klementiev, W. Grunert, E.D. Finashina, and L.M. Kustov J. Mol. Catal. A: Chem. 209 2004 97 106
8. E. Guibal Prog. Polym. Sci. 30 2005 71 109
9. R. Valentin, K. Molvinger, C. Viton, A. Domard, and F. Quignard Biomacromolecules 6 2005 2785 2792
10. F.P. Blondet, T. Vincent, and E. Guibal Int. J. Biol. Macromol. 43 2008 69 78
11. M.F. Zeng, Z.P. Fang, and C.W. Xu J. Appl. Polym. Sci. 91 2004 2840 2847
12. M.F. Zeng, Z.P. Fang, and C.W. Xu J. Membr. Sci. 230 2004 175 181
13. Y. de Miguel, T. Rohr, and D.C. Sherrington Structure, morphology, physical formats and characterization of polymer supports M. Buchmeiser, Polymeric materials in organic chemistry and catalysis 2003 Wiley-VCH Weinheim 1 52
14. J. Wang, H.F.M. Boelens, M.B. Thathagar, and G. Rothenberg ChemPhysChem. 5 2004 93 98
15. M.F. Zeng, Y.J. Du, L.J. Shao, C.Z. Qi, and X.-M. Zhang J. Org. Chem. 75 2010 2556 2563
16. L.J. Shao, Y.J. Du, M.F. Zeng, X.D. Li, W.T. Shen, S.F. Zuo, Y.Q. Lu, X.-M. Zhang, and C.Z. Qi Appl. Organometal. Chem. 24 2010 421 425
17. C.Z. Qi, X.D. Sun, C.Y. Lu, J.Z. Yang, Y.J. Du, H.J. Wu, and X.-M. Zhang J. Organomet. Chem. 694 2009 2912 2916
18. P.G. Tsyrul'nikov, T.N. Afonasenko, S.V. Koshcheev, and A.I. Boronin Kinet. Catal. 48 2007 728 734
19. K.S. Kim, A.F. Gossmann, and N. Winograd Anal. Chem. 46 1974 197 200
20. F. Peirano, T. Vincent, F. Quignard, M. Robitzer, and E. Guibal J. Membr. Sci. 329 2009 30 45
21. G. Bringmann, C. Günther, M. Ochse, O. Schupp, and S. Tasler W. Herz, H. Falk, G.W. Kirby, R.E. Moore, Biaryls in nature: a multi-facetted class of stereochemically, biosynthetically, and pharmacologically intriguing secondary metabolites 2001 Springer-Verlag Wien, New York 1 249
22. D.D. Hennings, T. Iwama, and V.H. Rawal Org. Lett. 1 1999 1205 1208
23. T. Mizoroki, K. Mori, and A. Ozaki Bull. Chem. Soc. Jpn. 44 1971 581 -581
24. R.F. Heck, and J.P. Nolley J. Org. Chem. 37 1972 2320 2322
25. N.T.S. Phan, M. Van Der Sluys, and C.W. Jones Adv. Synth. Catal. 348 2006 609 679
26. M. Oestreich The Mizoroki-Heck Reactions 2009 Wiley-VCH New York
27. S. Liu, and J. Xiao Toward green catalytic synthesis: transition metal catalyzed reactions in non-conventional media J. Mol. Catal. A 270 2007 1 43
28. A.D. Hea, and N.M. Jackson J. Phys. Org. Chem. 15 2002 52 55
29. I.P. Beletskaya Pure Appl. Chem. 74 2002 1327 1337
30. H.-U. Blaser, A. Indolse, F. Naud, U. Nettekoven, and A. Schnydev Adv. Synth. Catal. 346 2004 1583 1598
31. S. Brunauer, P.H. Emmett, and E. Teller J. Am. Chem. Soc. 60 1938 309 319
32. T.N. Glasnov, S. Findenig, and C.O. Kappe Chem. Eur. J. 15 2009 1001 1015
33. N. Hoshiya, N. Isomura, M. Shimoda, H. Yoshikawa, Y. Yamashita, K. Iizuka, S. Tsukamoto, S. Shuto, and M. Arisawa ChemCatChem. 1 2009 279 285
34. C.M. Crudden, M. Sateesh, and R. Lewis J. Am. Chem. Soc. 127 2005 10045 10050
35. F. Quignard, A. Choplin, and A. Domard Langmuir 16 2000 9106 9108
36. R.A. Sheldon, M. Wallau, I.W.C.E. Arends, and U. Schuchardt Acc. Chem. Res. 31 1998 485 493