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Pd(II) Catalyzed Copolymerization of Styrene and CO in Quaternary Ammonium Ionic Liquids  

Tian, Jing (School of Chemical Engineering and Technology, TianJin University)
Guo, Jin-Tang (School of Chemical Engineering and Technology, TianJin University)
Zhu, Cheng-Cai (School of Chemical Engineering and Technology, TianJin University)
Zhang, Xin (School of Chemical Engineering and Technology, TianJin University)
Xu, Yong-Shen (School of Chemical Engineering and Technology, TianJin University)
Publication Information
Macromolecular Research / v.17, no.3, 2009 , pp. 144-148 More about this Journal
Abstract
Poly(1-oxo-2-phenyltrimethylene) was synthesized by palladium-catalyzed copolymerization of styrene and carbon monoxide in quaternary ammonium ionic liquids. The $[Pd(bipy)_2][PF_6]_2$ compound had relatively more catalytic activity than $[Pd(bipy)_2][BF_4]_2$ in ionic liquids. The catalytic activity of palladium (II) composite catalyst was superior to the catalyst formed in situ from palladium acetate, 2,2-bipyridyl, and $X^-$ ($X^-=PF_6^-$, $BF_4^-$) in ionic liquids. The effects of the volume of ionic liquids, reaction time and benzoquinone content on the copolymerization were also described.
Keywords
poly(1-oxo-2-phenyltrimethylene); ionic liquids; palladium catalyst; carbon monoxide; catalytic activity;
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1 B. Pugin, M. Studer, E. Kuesters, G. Sedelmeier, and X. Feng, Advanced Synthesis & Catalysis, 346, 1481 (2004)   DOI   ScienceOn
2 H.-J. Wang, L.-L. Wang, W.-S. Lam, W.-Y. Yu, and Albert S. C. Chan, Tetrahedron, 17, 7 (2006)   DOI   ScienceOn
3 J. Durand and B. Milani, Chem. Rev., 250, 542 (2006)
4 C. G. Blanco, D. C. Banciella, and M. D. G. Azpiroz, J. Mol. Catal. A-Chem., 253, 203 (2006)   DOI   ScienceOn
5 B. Milani, A. Anzilutti, L. Vicentini, A. Sessanta o Santi, E. Zangrando, S. Geremia, and G. Mestroni, Organometallics, 16, 5064 (1997)   DOI   ScienceOn
6 P. Wasserscheid, C. Hilgers, C. M. Gordon, M. J. Muldoon, and I. R. Dunkin, Chem. Commun., 13, 1186 (2001)
7 C. Hardacre, J. D. Holbrey, S. P. Katdare, and K. R. Seddon, Green Chem., 4, 143 (2002)   DOI   ScienceOn
8 E. Drent and P. H. M. Budzelaar, Chem. Rev., 96, 663 (1996)   DOI   ScienceOn
9 P. Kubisa, Prog. Polym. Sci., 29, 3 (2004)   DOI   ScienceOn
10 W. C. J. Zuiderduin, D. S. Homminga, J. Huetink, and R. J. Gaymans, Polymer, 46, 1921 (2005)   DOI   ScienceOn
11 A. Balazs, C. Benedek, and S. Toros, J. Mol. Catal. A-Chem., 244, 105 (2006)   DOI   ScienceOn
12 A. J. Carmichael, D. M. Haddleton, S. A. F. Bon, and K. R. Seddon, Chem. Commun., 14, 1237 (2000)
13 A. Vavasori, G. Cavinato, and L. Toniolo, J. Mol. Catal. A-Chem., 191, 209 (2003)   DOI   ScienceOn
14 G. P. Belov and E. V. Novikova, Russian Chem. Rev., 73, 267 (2004)   DOI   ScienceOn
15 U. Domanska and R Bogel- ukasik, J. Phys. Chem. B, 109, 12124 (2005)   DOI   ScienceOn
16 A. Riisager, R. Fehrmann, M. Haumann, B. S. K. Gorle, and P. Wasserscheid, Ind. Eng. Chem. Res., 44, 9853 (2005)   DOI   ScienceOn
17 E. Drent and P. H. M. Budzelaar, J. Organomet. Chem., 593, 211 (2000)   DOI   ScienceOn
18 J. Durand, A. Scarel, B. Milani, and R. Seraglia, et al., Chimica Acta, 89, 1752 (2006)   DOI   ScienceOn