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1
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0012737536
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Japan Patent 08208736 (Chisso Corp.)
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(a) Matsukawa, T.; Kiba, R.; Ikeda, T. Japan Patent 08208736 (Chisso Corp.); Chem. Abstr. 1996, 125, 276902.
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Chem. Abstr.
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Matsukawa, T.1
Kiba, R.2
Ikeda, T.3
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2
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0012626711
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(b) Taeji, K.; Uozumi, T.; Soga, K. Polym. Prepr. Jpn. 1995, 44, 2.
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Polym. Prepr. Jpn.
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Taeji, K.1
Uozumi, T.2
Soga, K.3
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3
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0343785380
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Yokohama, Japan, October 26, paper 27A06
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(c) Kiyoshi, E.; Saitoh, M. Prepr. 7th SPSJ International Polymer Conference, Yokohama, Japan, October 26, 1999; paper 27A06.
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(1999)
Prepr. 7th SPSJ International Polymer Conference
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Kiyoshi, E.1
Saitoh, M.2
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4
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0003183565
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World Patent WO 9923124 A1 (Occidental Chemical)
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The free radical polymerization of VC initiated by group 4 metallocenes under photochemical conditions has been reported: Nagy, S. M.; Krishnamurti, R.; Cocoman, M. K.; Opalinski, W. M.; Smolka, T. F. World Patent WO 9923124 A1 (Occidental Chemical); Chem. Abstr. 1999, 130, 338530.
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Chem. Abstr.
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Nagy, S.M.1
Krishnamurti, R.2
Cocoman, M.K.3
Opalinski, W.M.4
Smolka, T.F.5
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5
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0343349594
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Ph.D. Thesis, California Institute of Technology, 1987
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Burger, B. Ph.D. Thesis, California Institute of Technology, 1987.
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Burger, B.1
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6
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0001685662
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Takahashi, T.; Kotora, M.; Fischer, R.; Nishihara, Y.; Nadajima, K. J. Am. Chem. Soc. 1995, 117, 11039.
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J. Am. Chem. Soc.
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Takahashi, T.1
Kotora, M.2
Fischer, R.3
Nishihara, Y.4
Nadajima, K.5
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7
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0032509942
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Hanzawa, Y.; Kowase, N.; Taguchi, T. Tetrahedron Lett. 1998, 39, 583.
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(1998)
Tetrahedron Lett.
, vol.39
, pp. 583
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Hanzawa, Y.1
Kowase, N.2
Taguchi, T.3
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8
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0028761731
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3 to generate cationic metal alkyl species: Yang, X.; Stern, C. L.; Marks, T. J. J. Am. Chem. Soc. 1994, 116, 10015.
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(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 10015
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Yang, X.1
Stern, C.L.2
Marks, T.J.3
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9
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0000182134
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(b) Generation of 1: Dagorne, S.; Rodewald, S.; Jordan, R. F. Organometallics 1997, 16, 5541.
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(1997)
Organometallics
, vol.16
, pp. 5541
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Dagorne, S.1
Rodewald, S.2
Jordan, R.F.3
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10
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0342480168
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note
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3, the precursors of 1, reacts with VC under these conditions.
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12
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0342480165
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note
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1H NMR assuming one unsaturated end group per chain.
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13
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0342480164
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note
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3 region, J in Hz) major isomer, δ 6.82 (d, J = 3, 1H), 6.48 (d, 7 = 3, 1H), 6.10 (d, J = 3, 1H), 5.91 (d, J = 3, 1H); minor isomer, 6.78 (d, J = 3, 1H), 6.38 (d, J = 3, 1H), 6.32 (d, J = 3, 1H), 5.96 (d, J = 3, 1H).
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14
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0343349585
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note
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3Bn]Cl to a mixture of 4 and 2 results in complete conversion to 3.
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15
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0004207538
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Fink, G., Mulhaupt, R., Brintzinger, H. H., Eds.; Springer-Verlag: New York
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Brintzinger, H. H. In Ziegler Catalysts; Fink, G., Mulhaupt, R., Brintzinger, H. H., Eds.; Springer-Verlag: New York, 1995; p 181.
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(1995)
Ziegler Catalysts
, pp. 181
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Brintzinger, H.H.1
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16
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33749125170
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Bochmann, M.; Lancaster, S. J. Angew. Chem., Int. Ed. Engl. 1994, 33, 1634.
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(1994)
Angew. Chem., Int. Ed. Engl.
, vol.33
, pp. 1634
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Bochmann, M.1
Lancaster, S.J.2
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17
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0000869075
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(a) Resconi, L.; Fait, A.; Piemontesi, F.; Colonnesi, M.; Rychlicki, H.; Zeigler, R. Macromolecules 1995, 28, 6667.
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(1995)
Macromolecules
, vol.28
, pp. 6667
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Resconi, L.1
Fait, A.2
Piemontesi, F.3
Colonnesi, M.4
Rychlicki, H.5
Zeigler, R.6
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19
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0343785375
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note
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3, and oligopropylene; in this case the chloride in 3 must derive from VC.
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20
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0342480161
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note
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- anion is unchanged.
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21
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0343785374
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note
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13C NMR.
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22
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0001203620
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Burger, B. J.; Thompson, M. E.; Cotter, W. D.; Bercaw, J. E. J. Am. Chem. Soc. 1990, 112, 1566.
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(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 1566
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Burger, B.J.1
Thompson, M.E.2
Cotter, W.D.3
Bercaw, J.E.4
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