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Volumn 116, Issue 11, 1994, Pages 4623-4640

Model Ziegler-Natta α-Olefin Polymerization Catalysts Derived from [{(η5-C5Me4)SiMe2(η1-NCMe3)KPMe3)Sc(μ2-H)]2 and [{(η5-C5Me4)SiMe2(η1-NCMe3)}Sc(M2-CH2CH2CH3)]2. Synthesis, Structures, and Kinetic and Equilibrium Investigations of the Catalytically Active Species in Solution

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EID: 0000748027     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00090a011     Document Type: Article
Times cited : (504)

References (62)
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    • There has been some recent interest in the application of this ligand system to Ti-, Zr-, and Hf-based catalysts for ethylene/1-alkene co-polymerizations; see, for example: Eur. Patent 420 436, Canich, J. M.; HIatky, G. G.; Turner, H. W. U.S. Patent 542 236, 1990; Stevens, J. C.; Timmers, F. J.; Wilson, D. R.; Schmidt, G. F.; Nickias, P. N.; Rosen, R. K.; Knight, G. W.; Lai, S. Eur. Patent 416 815, 1990.
    • There has been some recent interest in the application of this ligand system to Ti-, Zr-, and Hf-based catalysts for ethylene/1-alkene co-polymerizations; see, for example: Canich, J. M. Eur. Patent 420 436, 1991; Canich, J. M.; HIatky, G. G.; Turner, H. W. U.S. Patent 542 236, 1990; Stevens, J. C.; Timmers, F. J.; Wilson, D. R.; Schmidt, G. F.; Nickias, P. N.; Rosen, R. K.; Knight, G. W.; Lai, S. Eur. Patent 416 815, 1990.
    • (1991)
    • Canich, J.M.1
  • 27
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    • Very recently a related but unlinked ligand system has been employed with yttrium to achieve olefin polymerizations:
    • Very recently a related but unlinked ligand system has been employed with yttrium to achieve olefin polymerizations: Schaverien, C. J. Organometallics 1994, 13, 69.
    • (1994) Organometallics , vol.13 , pp. 69
    • Schaverien, C.J.1
  • 36
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    • For other examples of compounds with this type of bridging, 5-coordinate carbon center see: (a)
    • For other examples of compounds with this type of bridging, 5-coordinate carbon center see: (a) Holton, J.; Lappert, M. F.; Pearce, R.; Yarrow, P. I. Chem. Rev. 1983, 83, 135.
    • (1983) Chem. Rev. , vol.83 , pp. 135
    • Holton, J.1    Lappert, M.F.2    Pearce, R.3    Yarrow, P.I.4
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    • Similar chemistry is observed for THF adducts of zirconocene cations.
    • Similar chemistry is observed for THF adducts of zirconocene cations. Jordan, R. F.; Bajgur, C. S.; Willett, R.; Scott, B. J. Am. Chem. Soc. 1986, 108, 7410.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 7410
    • Jordan, R.F.1    Bajgur, C.S.2    Willett, R.3    Scott, B.4
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    • Wayda, A. L., Darensbourg, M. Y., Eds.; ACS Symp. Ser. No. 357; American Chemical Society: Washington, DC, 1987; pp 79-98.
    • Burger, B. J.; Bercaw, J. E. In Experimental Organometallic Chemistry; Wayda, A. L., Darensbourg, M. Y., Eds.; ACS Symp. Ser. No. 357; American Chemical Society: Washington, DC, 1987; pp 79-98.
    • Experimental Organometallic Chemistry
    • Burger, B.J.1    Bercaw, J.E.2
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