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Johnson, L.K.1
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(b) Gates, D. P.; Svejda, S. A.; Oñate, E.; Killian, C. M.; Johnson, L. K.; White, P. S.; Brookhart, M. Macromolecules 2000, 33, 2320.
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3
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0011462462
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WO 96/23010 (to DuPont); [Chem. Abstr. 1996, 125, 22273t]
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(c) Johnson, J. K.; Killian, C. M.; Arthur, S. D.; Feldman, J.; McCord, E. F.; McLain, S. J.; Kreutzer, K. A.; Bennett, A. M. A.; Coughlin, E. B.; Ittel, S. D.; Parthasarathy, A.; Tempel, D. J.; Brookhart, M. WO 96/23010 (to DuPont) 1996 [Chem. Abstr. 1996, 125, 22273t].
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Johnson, J.K.1
Killian, C.M.2
Arthur, S.D.3
Feldman, J.4
McCord, E.F.5
McLain, S.J.6
Kreutzer, K.A.7
Bennett, A.M.A.8
Coughlin, E.B.9
Ittel, S.D.10
Parthasarathy, A.11
Tempel, D.J.12
Brookhart, M.13
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4
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0011414471
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WO 01/10876 (to BP Chemicals)
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Wass, D. F. WO 01/10876 (to BP Chemicals).
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Wass, D.F.1
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5
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0011477464
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We have recently reported the activity of these ligands in palladium-catalyzed ethylene/CO copolymerization: (a) Dossett, S. J. WO 97/37765 (to BP Chemicals).
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Dossett, S.J.1
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6
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0011512494
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WO 00/06299 (to BP Chemicals)
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(b) Dossett, S. J. WO 00/06299 (to BP Chemicals).
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Dossett, S.J.1
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7
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0035926115
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(c) Dossett, S. J.; Gillon, A.; Orpen, A. G.; Fleming, J. S.; Pringle, P. G.; Wass, D. F.; Jones, M. D. Chem. Commun. 2001, 699.
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Dossett, S.J.1
Gillon, A.2
Orpen, A.G.3
Fleming, J.S.4
Pringle, P.G.5
Wass, D.F.6
Jones, M.D.7
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8
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0033557814
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(a) Britovsek, G. J. P.; Gibson, V. C.; Wass, D. F. Angew. Chem., Int. Ed. 1999, 38, 429.
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Ittel, S.D.1
Johnson, L.K.2
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84984681550
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Mixed hard/soft ligands produce polyethylene under certain conditions: (a) Keim, W.; Kowaldt, F. H.; Goddard, R.; Kruger, C. Angew. Chem., Int. Ed. Engl. 1978, 17, 466.
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(b) Keim, W.; Appel, R.; Gruppe, S.; Knoch, F. Angew. Chem., Int. Ed. Engl. 1987, 26, 1012.
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Keim, W.1
Appel, R.2
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(d) Klabunde, U.; Mulhaupt, R.; Herskovitz, T.; Janowicz, A. H.; Calabrese, J.; Ittel, S. D. J. Polym. Sci., Part A: Polym. Chem. 1987, 25, 1989.
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Ittel, S.D.6
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14
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0000041191
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Notably, palladium phosphine catalysts are well established for the copolymerisation of olefins and carbon monoxide. See: Drent, E.; Budzelaar, P. H. M. Chem. Rev. 1996, 96, 663.
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Drent, E.1
Budzelaar, P.H.M.2
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15
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0034249672
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For a recent general overview of the use of phosphine ligands in catalysis, see: van Leeuwen, P. W. N. M.; Kamer, P. C. J.; Reek, J. N. H.; Diekes, P. Chem. Rev. 2000, 100, 2741.
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Kamer, P.C.J.2
Reek, J.N.H.3
Diekes, P.4
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16
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79959372448
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Chelating diphosphine ligands demonstrate extremely low activity and give low molecular weight products: (a) Mui, H. D.; Riehl, M. E.; Wilson, S. R.; Girolami, G. S. ACS Abstracts 1994, Vol. 208 (part 1), pp 530-INOR.
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Mui, H.D.1
Riehl, M.E.2
Wilson, S.R.3
Girolami, G.S.4
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21
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0034695625
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(b) Younkin, T. R.; Connor, E. F.; Henderson, J. I.; Friedrich, S. K.; Grubbs, R. H.; Bansleben, D. A. Science 2000, 287, 460.
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Science
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Younkin, T.R.1
Connor, E.F.2
Henderson, J.I.3
Friedrich, S.K.4
Grubbs, R.H.5
Bansleben, D.A.6
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22
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0011514581
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note
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1, T = 173 K, 4119 unique data, Rl = 0.0280. Molecules of 2a have exact crystallographic Cz symmetry.
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24
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0033740669
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Similar effects have been observed for metallocene-type catalysts. For a discussion of this and a recent review of MAO cocatalysts in general, see: Chen, E. Y.-X.; Marks, T. J. Chem Rev. 2000, 100, 1391.
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Chem Rev.
, vol.100
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Chen, E.Y.-X.1
Marks, T.J.2
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25
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0011459932
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note
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1H NMR spectroscopy (see Supporting Information).
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26
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0011504780
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See Supporting Information
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See Supporting Information.
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27
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0011514732
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A typical profile is included in the Supporting Information
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A typical profile is included in the Supporting Information.
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28
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0033732391
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For a recent review of support strategies, mainly in the metallocene area, see: Hlatky, G. G. Chem. Rev. 2000, 100, 1347.
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Chem. Rev.
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Hlatky, G.G.1
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