Synthesis, molecular structures and norbornene addition polymerization activity of the neutral nickel catalysts supported by N-naphthyl- salicylaldiminato ligands

Inorganic Chemistry Communications

Volumn 8, Issue 1, 2005, Pages 109-112

  Wang, Wei Hua ^a   Jin, Guo Xin ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

Catalysts; Molecular structure; Nickel; Polymerization; Polynorbornene

Indexed keywords

NICKEL; NORBORNENE DERIVATIVE; SALICYLAMIDE DERIVATIVE;

ADDITION REACTION; ARTICLE; CATALYSIS; INFRARED SPECTROSCOPY; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYMERIZATION; SYNTHESIS;

EID: 10944241044     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2004.11.025     Document Type: Article

References (31)

1. S.D. Ittel, L.K. Johnson, and M. Brookhart Chem. Rev. 100 2000 1169
2. G.W. Coates Chem. Rev. 100 2000 1223
3. S. Mecking Coord. Chem. Rev. 203 2000 325
4. V.C. Gibson, and S.K. Spitzmesser Chem. Rev. 103 2003 283
5. L.K. Johnson, C.M. Killian, and M. Brookhart J. Am. Chem. Soc. 117 1995 6414
6. D.P. Gates, S.A. Svejda, E. Onate, C.M. Killian, L.K. Johnson, P.S. White, and M. Brookhart Macromolecules 33 2000 2320
7. Z. Guan, P.M. Cotts, E.F. McCord, and S.J. McLain Science 283 1999 2059
8. C.M. Killian, D.J. Tempel, L.K. Johnson, and M. Brookhart J. Am. Chem. Soc. 118 1996 11664
9. R. Soula, J.P. Broyer, M.F. Llauro, A. Tomov, R. Spitz, J. Claverie, X. Drujon, J. Malinge, and T. Saudemont Macromolecules 34 2001 2438
10. C. Wang, S. Friedrich, T.R. Younkin, R.T. Li, R.H. Grubbs, D.A. Bansleben, and M.W. Day Organometallics 17 1998 3149
11. T.R. Younkin, E.F. Connor, J.I. Henderson, S.K. Friedrich, R.H. Grubbs, and D.A. Bansleben Science 287 2000 460
12. D. Zhang, and G.X. Jin Chem Commun. 2002 574
13. D. Zhang, and G.X. Jin Eur. J. Inorg. Chem. 2003 1570
14. D. Zhang, and G.X. Jin Appl. Catal. A: General 262 2004 13
15. D. Zhang, and G.X. Jin Appl. Catal. A: General 262 2004 85
16. G.X. Jin, and D. Zhang J. Polym. Sci. Polym. Chem. 42 2004 1018
17. D. Zhang, and G.X. Jin Organometallics 22 2003 2851
18. T.J. Deming, and B.M. Novak Macromolecules 26 1993 7089
19. A.O. Patil, S. Zushma, R.T. Stibrany, S.P. Rucker, and L.M. Wheeler J. Polym. Sci. Part A: Polym. Chem. 41 2003 2095
20. X.F. Li, and Y.S. Li J. Polym. Sci. Part A: Poly. Chem. 40 2002 2680
21. W.H. Sun, H. Yang, Z. Li, and Y. Li Organometallics 22 2003 3678
22. V. Lozan, P.G. Lassahn, C. Zhang, B. Wu, C. Janiak, G. Rheinwald, and Z. Lang Z. Naturforsch. B 58 2003 1152
23. G.M. Benedikt, E. Elce, B.L. Goodall, H.A. Kalamarides, L.H. McIntosh, L.F. Rhodes, K.T. Selvy, C. Andes, K. Oyler, and A. Sen Macromolecules 35 2002 8979
24. X. Mi, Z. Ma, N. Cui, L. Wang, Y. Ke, and Y. Hu J. Appl. Poly. Sci. 88 2003 3273
25. D. Zhang, G.X. Jin, L.H. Weng, and F.S. Wang Organometallics 23 2004 3270
26. 6: C, 75.86; H, 5.25; N, 2.21. Found: C, 75.93; H, 5.71; N, 2.43
27. 2 by a full-matrix least-squares method. Anisotropic displacement parameters were included for all non-hydrogen atoms. All the calculations were carried out with Siemens SHELXTL PLUS program. Crystallographic data for the structural analysis have been deposited with the Cambridge Crystallographic Data Center CCDC Nos. 248435 and 248436
28. S.Y. Desjardins, K.J. Cavell, J.L. Hoare, B.W. Skelton, A.N. Sobolev, A.H. White, and W. Keim J. Organomet. Chem. 544 1997 163
29. C. Mast, M. Krieger, K. Dehnicke, and A. Greiner Macromol. Rapid Commun. 20 1999 232
30. Determined using a PL GPC-220 gel permeation chromatograph at 150°C with narrow standard calibration and equipped with three PL gel columns (sets of PL gel 10 μm Mixed-B LS), and 1,2,4-trichlorobenzene was used as solvent at a flow rate of 1.00 ml/min
31. 13C NMR (o-dichlorobenzene-d4): δ = 29-52 ppm (m, maxima at 31.1, 38.1, 47.1)