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Volumn 15, Issue 2, 1996, Pages 693-703

Ethylene, styrene, and α-methylstyrene polymerization by mono(pentamethylcyclopentadienyl) (Cp*) complexes of titanium, zirconium, and hafnium: Roles of cationic complexes of the type [Cp*MR2]+ (R = alkyl) as both coordination polymerization catalysts and carbocationic polymerization initiators

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EID: 0038049969     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9501945     Document Type: Article
Times cited : (148)

References (93)
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    • See, for instance: (a) Kaminsky, W., Sinn, H., Eds. Transition Metals and Organometallics as Catalysts for Olefin Polymerization; Springer-Verlag: Berlin, 1988. (b) Quirk, R. P., Ed. Transition Metal Catalyzed Polymerizations; Ziegler-Natta and Metathesis Polymerizations; Cambridge University Press: Cambridge, U.K., 1988. (c) Mohring, P. C.; Coville, N. J. J. Organomet. Chem. 1994, 479, 1. (d) Gupta, V. K.; Satish, S.; Bhardway, I. S. J. Macromol. Sci. 1994, C34, 439. (e) Brintzinger, H. H.; Fischer, D.; Mülhaupt, R.; Rieger, B.; Waymouth, R. M. Angew. Chem., Int. Ed. Engl. 1995, 34, 1143. For recent theoretical considerations at the density functional level, see: (f) Woo, T. K.; Fan, L.; Ziegler, T. Organometallics 1994, 13, 2252. (g) Weiss, H.; Ehrig, M.; Ahlrichs, R. J. Am. Chem. Soc. 1994, 116, 4919. For counterion effects, see: (h) Chien, J. C. W.; Song, Y.; Rausch, M. D. J. Polym. Sci.: Part A 1994, 32, 2387.
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    • See, for instance: (a) Kaminsky, W., Sinn, H., Eds. Transition Metals and Organometallics as Catalysts for Olefin Polymerization; Springer-Verlag: Berlin, 1988. (b) Quirk, R. P., Ed. Transition Metal Catalyzed Polymerizations; Ziegler-Natta and Metathesis Polymerizations; Cambridge University Press: Cambridge, U.K., 1988. (c) Mohring, P. C.; Coville, N. J. J. Organomet. Chem. 1994, 479, 1. (d) Gupta, V. K.; Satish, S.; Bhardway, I. S. J. Macromol. Sci. 1994, C34, 439. (e) Brintzinger, H. H.; Fischer, D.; Mülhaupt, R.; Rieger, B.; Waymouth, R. M. Angew. Chem., Int. Ed. Engl. 1995, 34, 1143. For recent theoretical considerations at the density functional level, see: (f) Woo, T. K.; Fan, L.; Ziegler, T. Organometallics 1994, 13, 2252. (g) Weiss, H.; Ehrig, M.; Ahlrichs, R. J. Am. Chem. Soc. 1994, 116, 4919. For counterion effects, see: (h) Chien, J. C. W.; Song, Y.; Rausch, M. D. J. Polym. Sci.: Part A 1994, 32, 2387.
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    • (1994) J. Macromol. Sci. , vol.C34 , pp. 439
    • Gupta, V.K.1    Satish, S.2    Bhardway, I.S.3
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    • 33746295241 scopus 로고
    • See, for instance: (a) Kaminsky, W., Sinn, H., Eds. Transition Metals and Organometallics as Catalysts for Olefin Polymerization; Springer-Verlag: Berlin, 1988. (b) Quirk, R. P., Ed. Transition Metal Catalyzed Polymerizations; Ziegler-Natta and Metathesis Polymerizations; Cambridge University Press: Cambridge, U.K., 1988. (c) Mohring, P. C.; Coville, N. J. J. Organomet. Chem. 1994, 479, 1. (d) Gupta, V. K.; Satish, S.; Bhardway, I. S. J. Macromol. Sci. 1994, C34, 439. (e) Brintzinger, H. H.; Fischer, D.; Mülhaupt, R.; Rieger, B.; Waymouth, R. M. Angew. Chem., Int. Ed. Engl. 1995, 34, 1143. For recent theoretical considerations at the density functional level, see: (f) Woo, T. K.; Fan, L.; Ziegler, T. Organometallics 1994, 13, 2252. (g) Weiss, H.; Ehrig, M.; Ahlrichs, R. J. Am. Chem. Soc. 1994, 116, 4919. For counterion effects, see: (h) Chien, J. C. W.; Song, Y.; Rausch, M. D. J. Polym. Sci.: Part A 1994, 32, 2387.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1143
    • Brintzinger, H.H.1    Fischer, D.2    Mülhaupt, R.3    Rieger, B.4    Waymouth, R.M.5
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    • See, for instance: (a) Kaminsky, W., Sinn, H., Eds. Transition Metals and Organometallics as Catalysts for Olefin Polymerization; Springer-Verlag: Berlin, 1988. (b) Quirk, R. P., Ed. Transition Metal Catalyzed Polymerizations; Ziegler-Natta and Metathesis Polymerizations; Cambridge University Press: Cambridge, U.K., 1988. (c) Mohring, P. C.; Coville, N. J. J. Organomet. Chem. 1994, 479, 1. (d) Gupta, V. K.; Satish, S.; Bhardway, I. S. J. Macromol. Sci. 1994, C34, 439. (e) Brintzinger, H. H.; Fischer, D.; Mülhaupt, R.; Rieger, B.; Waymouth, R. M. Angew. Chem., Int. Ed. Engl. 1995, 34, 1143. For recent theoretical considerations at the density functional level, see: (f) Woo, T. K.; Fan, L.; Ziegler, T. Organometallics 1994, 13, 2252. (g) Weiss, H.; Ehrig, M.; Ahlrichs, R. J. Am. Chem. Soc. 1994, 116, 4919. For counterion effects, see: (h) Chien, J. C. W.; Song, Y.; Rausch, M. D. J. Polym. Sci.: Part A 1994, 32, 2387.
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    • See, for instance: (a) Kaminsky, W., Sinn, H., Eds. Transition Metals and Organometallics as Catalysts for Olefin Polymerization; Springer-Verlag: Berlin, 1988. (b) Quirk, R. P., Ed. Transition Metal Catalyzed Polymerizations; Ziegler-Natta and Metathesis Polymerizations; Cambridge University Press: Cambridge, U.K., 1988. (c) Mohring, P. C.; Coville, N. J. J. Organomet. Chem. 1994, 479, 1. (d) Gupta, V. K.; Satish, S.; Bhardway, I. S. J. Macromol. Sci. 1994, C34, 439. (e) Brintzinger, H. H.; Fischer, D.; Mülhaupt, R.; Rieger, B.; Waymouth, R. M. Angew. Chem., Int. Ed. Engl. 1995, 34, 1143. For recent theoretical considerations at the density functional level, see: (f) Woo, T. K.; Fan, L.; Ziegler, T. Organometallics 1994, 13, 2252. (g) Weiss, H.; Ehrig, M.; Ahlrichs, R. J. Am. Chem. Soc. 1994, 116, 4919. For counterion effects, see: (h) Chien, J. C. W.; Song, Y.; Rausch, M. D. J. Polym. Sci.: Part A 1994, 32, 2387.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4919
    • Weiss, H.1    Ehrig, M.2    Ahlrichs, R.3
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    • See, for instance: (a) Kaminsky, W., Sinn, H., Eds. Transition Metals and Organometallics as Catalysts for Olefin Polymerization; Springer-Verlag: Berlin, 1988. (b) Quirk, R. P., Ed. Transition Metal Catalyzed Polymerizations; Ziegler-Natta and Metathesis Polymerizations; Cambridge University Press: Cambridge, U.K., 1988. (c) Mohring, P. C.; Coville, N. J. J. Organomet. Chem. 1994, 479, 1. (d) Gupta, V. K.; Satish, S.; Bhardway, I. S. J. Macromol. Sci. 1994, C34, 439. (e) Brintzinger, H. H.; Fischer, D.; Mülhaupt, R.; Rieger, B.; Waymouth, R. M. Angew. Chem., Int. Ed. Engl. 1995, 34, 1143. For recent theoretical considerations at the density functional level, see: (f) Woo, T. K.; Fan, L.; Ziegler, T. Organometallics 1994, 13, 2252. (g) Weiss, H.; Ehrig, M.; Ahlrichs, R. J. Am. Chem. Soc. 1994, 116, 4919. For counterion effects, see: (h) Chien, J. C. W.; Song, Y.; Rausch, M. D. J. Polym. Sci.: Part A 1994, 32, 2387.
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    • U.S. Patent 5,023,304, Jun 11, 1991 (to Idemitsu Kosan Co., Tokyo, Japan)
    • For representative, recent patents describing catalyst systems similar to those described here: (a) Takeuchi, M.; Kuramoto, M. U.S. Patent 5,023,304, Jun 11, 1991 (to Idemitsu Kosan Co., Tokyo, Japan). (b) Campbell, R. E. U.S. Patent 5,066,741, Nov 19, 1991 (to The Dow Chemical Co., Midland, MI). (c) Canich, J. A. M. U.S. Patent 5,096, 867, Mar 17, 1992 (to Exxon Chemical Patents, Inc., Linden, NJ). (d) Stevens, J. C.; Neithamer, D. R. U.S. Patent 5,132,380, Jul 21, 1992 (to The Dow Chemical Co., Midland, MI). (e) Campbell, R. E. European Patent 597961, May 25, 1994 (to The Dow Chemical Co., Midland, MI).
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    • U.S. Patent 5,066,741, Nov 19, 1991 (to The Dow Chemical Co., Midland, MI)
    • For representative, recent patents describing catalyst systems similar to those described here: (a) Takeuchi, M.; Kuramoto, M. U.S. Patent 5,023,304, Jun 11, 1991 (to Idemitsu Kosan Co., Tokyo, Japan). (b) Campbell, R. E. U.S. Patent 5,066,741, Nov 19, 1991 (to The Dow Chemical Co., Midland, MI). (c) Canich, J. A. M. U.S. Patent 5,096, 867, Mar 17, 1992 (to Exxon Chemical Patents, Inc., Linden, NJ). (d) Stevens, J. C.; Neithamer, D. R. U.S. Patent 5,132,380, Jul 21, 1992 (to The Dow Chemical Co., Midland, MI). (e) Campbell, R. E. European Patent 597961, May 25, 1994 (to The Dow Chemical Co., Midland, MI).
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    • U.S. Patent 5,096, 867, Mar 17, 1992 (to Exxon Chemical Patents, Inc., Linden, NJ)
    • For representative, recent patents describing catalyst systems similar to those described here: (a) Takeuchi, M.; Kuramoto, M. U.S. Patent 5,023,304, Jun 11, 1991 (to Idemitsu Kosan Co., Tokyo, Japan). (b) Campbell, R. E. U.S. Patent 5,066,741, Nov 19, 1991 (to The Dow Chemical Co., Midland, MI). (c) Canich, J. A. M. U.S. Patent 5,096, 867, Mar 17, 1992 (to Exxon Chemical Patents, Inc., Linden, NJ). (d) Stevens, J. C.; Neithamer, D. R. U.S. Patent 5,132,380, Jul 21, 1992 (to The Dow Chemical Co., Midland, MI). (e) Campbell, R. E. European Patent 597961, May 25, 1994 (to The Dow Chemical Co., Midland, MI).
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    • U.S. Patent 5,132,380, Jul 21, 1992 (to The Dow Chemical Co., Midland, MI)
    • For representative, recent patents describing catalyst systems similar to those described here: (a) Takeuchi, M.; Kuramoto, M. U.S. Patent 5,023,304, Jun 11, 1991 (to Idemitsu Kosan Co., Tokyo, Japan). (b) Campbell, R. E. U.S. Patent 5,066,741, Nov 19, 1991 (to The Dow Chemical Co., Midland, MI). (c) Canich, J. A. M. U.S. Patent 5,096, 867, Mar 17, 1992 (to Exxon Chemical Patents, Inc., Linden, NJ). (d) Stevens, J. C.; Neithamer, D. R. U.S. Patent 5,132,380, Jul 21, 1992 (to The Dow Chemical Co., Midland, MI). (e) Campbell, R. E. European Patent 597961, May 25, 1994 (to The Dow Chemical Co., Midland, MI).
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    • European Patent 597961, May 25, 1994 (to The Dow Chemical Co., Midland, MI)
    • For representative, recent patents describing catalyst systems similar to those described here: (a) Takeuchi, M.; Kuramoto, M. U.S. Patent 5,023,304, Jun 11, 1991 (to Idemitsu Kosan Co., Tokyo, Japan). (b) Campbell, R. E. U.S. Patent 5,066,741, Nov 19, 1991 (to The Dow Chemical Co., Midland, MI). (c) Canich, J. A. M. U.S. Patent 5,096, 867, Mar 17, 1992 (to Exxon Chemical Patents, Inc., Linden, NJ). (d) Stevens, J. C.; Neithamer, D. R. U.S. Patent 5,132,380, Jul 21, 1992 (to The Dow Chemical Co., Midland, MI). (e) Campbell, R. E. European Patent 597961, May 25, 1994 (to The Dow Chemical Co., Midland, MI).
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    • note
    • (c) The PS reaction products obtained in ref 5b were all extracted with acetone to separate a-PS and s-PS, since it was not then realized that small amounts of very high molecular weight a-PS present in several cases were not soluble in acetone. The a-PS and s-PS in these materials were therefore not completely separated but were detected as separate bands in GPC measurements on supposed s-PS samples and mistakenly taken to be relatively low molecular weight s-PS.
  • 46
  • 48
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    • note
    • 2 results in the appearances of new Ti-Me resonances at δ 0.29, 0.20, and 0.08.
  • 62
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    • Private communication
    • (j) Bochmann, M. Private communication.
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    • note
    • 4h that the sample contained residual acetone from the extraction procedure seems quite unlikely in view of the conditions under which the material was dried.
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  • 85
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    • note
    • 2Me all occur in the region δ 0.8-1.3.
  • 86
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    • note
    • 3).
  • 92
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    • Reference 11, section 1.1.2
    • Reference 11, section 1.1.2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.