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1
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6544241298
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(a) Johnson, L. K.; Killian, C. M.; Brookhart, M. J. Am. Chem. Soc. 1995, 117, 6414.
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(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 6414
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Johnson, L.K.1
Killian, C.M.2
Brookhart, M.3
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2
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0142070493
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(b) Johnson, L. K.; Mecking, S.; Brookhart, M. J. Am. Chem. Soc. 1996, 118, 267.
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(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 267
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Johnson, L.K.1
Mecking, S.2
Brookhart, M.3
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4
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0009726492
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(b) Sen, A.; Lai, T.; Thomas, R. R. J. Organomet. Chem. 1988, 358, 567.
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(1988)
J. Organomet. Chem.
, vol.358
, pp. 567
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Sen, A.1
Lai, T.2
Thomas, R.R.3
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5
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5244340584
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Experimental details are given in the Supporting Information
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Experimental details are given in the Supporting Information.
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6
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33845278206
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unpublished results
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- is a relatively coordinating anion: Beck, W.; Sünkel, K. Chem. Rev. 1988, 88, 1405.
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McLain, S.J.1
Feldman, J.2
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7
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33845278206
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- is a relatively coordinating anion: Beck, W.; Sünkel, K. Chem. Rev. 1988, 88, 1405.
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(1988)
Chem. Rev.
, vol.88
, pp. 1405
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Beck, W.1
Sünkel, K.2
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8
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85088076615
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note
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n = 1.4) vs linear polyethylene; polymer contained 100 methyl-ended branches per 1000 methylene units.
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-
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9
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85088076338
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note
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n = 1.9) vs linear polyethylene in trichlorobenzene.
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-
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10
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5244257769
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note
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6Pd: C, 50.94; H, 6.17; N, 9.90. Found: C, 50.52; H, 6.17; N, 959.
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-
-
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11
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85088078619
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note
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n = 1.8) vs linear polyethylene; polymer contained 94 methyl-ended branches per 1000 methylene units.
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18
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0001212961
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(g) Mehler, C.; Risse, W. Makromol. Chem., Rapid Commun. 1991, 12, 255.
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(1991)
Makromol. Chem., Rapid Commun.
, vol.12
, pp. 255
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Mehler, C.1
Risse, W.2
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19
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0000468409
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(h) Mehler, C.; Risse, W. Makromol. Chem., Rapid Commun. 1992, 13, 455.
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(1992)
Makromol. Chem., Rapid Commun.
, vol.13
, pp. 455
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Mehler, C.1
Risse, W.2
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22
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0001059457
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9gj The recent preparation of well-defined Pd(II) alkyl and allyl catalysts for norbornene/norbornadiene polymerizations also suggests an insertion type mechanism: (a) Safir, A. L.; Novak, B. M. Macromolecules 1995, 28, 5396. (b) Safir, A. L.; Novak, B. M. Polym. Prepr., Am. Chem. Soc. Div. Polym. Chem. 1994, 35, 901. (c) Goodall, B. L.; Benedikt, G. M.; McIntosh, L. H.; Barnes, D. A. U.S. Patent 5, 468, 819, Nov 21, 1995. (d) Reinmuth, A.; Mathew, J. P.; Melia, J.; Risse, W. Makromol. Chem., Rapid Commun. 1996, 17, 173.
-
(1995)
Macromolecules
, vol.28
, pp. 5396
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Safir, A.L.1
Novak, B.M.2
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23
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5244301487
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9gj The recent preparation of well-defined Pd(II) alkyl and allyl catalysts for norbornene/norbornadiene polymerizations also suggests an insertion type mechanism: (a) Safir, A. L.; Novak, B. M. Macromolecules 1995, 28, 5396. (b) Safir, A. L.; Novak, B. M. Polym. Prepr., Am. Chem. Soc. Div. Polym. Chem. 1994, 35, 901. (c) Goodall, B. L.; Benedikt, G. M.; McIntosh, L. H.; Barnes, D. A. U.S. Patent 5, 468, 819, Nov 21, 1995. (d) Reinmuth, A.; Mathew, J. P.; Melia, J.; Risse, W. Makromol. Chem., Rapid Commun. 1996, 17, 173.
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(1994)
Polym. Prepr., Am. Chem. Soc. Div. Polym. Chem.
, vol.35
, pp. 901
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Safir, A.L.1
Novak, B.M.2
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24
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5244375310
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U.S. Patent 5, 468, 819, Nov 21, 1995
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9gj The recent preparation of well-defined Pd(II) alkyl and allyl catalysts for norbornene/norbornadiene polymerizations also suggests an insertion type mechanism: (a) Safir, A. L.; Novak, B. M. Macromolecules 1995, 28, 5396. (b) Safir, A. L.; Novak, B. M. Polym. Prepr., Am. Chem. Soc. Div. Polym. Chem. 1994, 35, 901. (c) Goodall, B. L.; Benedikt, G. M.; McIntosh, L. H.; Barnes, D. A. U.S. Patent 5, 468, 819, Nov 21, 1995. (d) Reinmuth, A.; Mathew, J. P.; Melia, J.; Risse, W. Makromol. Chem., Rapid Commun. 1996, 17, 173.
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-
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Goodall, B.L.1
Benedikt, G.M.2
McIntosh, L.H.3
Barnes, D.A.4
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25
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0030527991
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9gj The recent preparation of well-defined Pd(II) alkyl and allyl catalysts for norbornene/norbornadiene polymerizations also suggests an insertion type mechanism: (a) Safir, A. L.; Novak, B. M. Macromolecules 1995, 28, 5396. (b) Safir, A. L.; Novak, B. M. Polym. Prepr., Am. Chem. Soc. Div. Polym. Chem. 1994, 35, 901. (c) Goodall, B. L.; Benedikt, G. M.; McIntosh, L. H.; Barnes, D. A. U.S. Patent 5, 468, 819, Nov 21, 1995. (d) Reinmuth, A.; Mathew, J. P.; Melia, J.; Risse, W. Makromol. Chem., Rapid Commun. 1996, 17, 173.
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(1996)
Makromol. Chem., Rapid Commun.
, vol.17
, pp. 173
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Reinmuth, A.1
Mathew, J.P.2
Melia, J.3
Risse, W.4
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26
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3242847492
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Novak, B. M.; Safir, A. L. Polym. Prepr., Am. Chem. Soc. Div. Polym. Chem. 1996, 37, 335.
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(1996)
Polym. Prepr., Am. Chem. Soc. Div. Polym. Chem.
, vol.37
, pp. 335
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Novak, B.M.1
Safir, A.L.2
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27
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85088075939
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note
-
n = 670). Thus, water appears to serve as a chain transfer agent. We further conclude that, if adventitious water is playing a role in catalyst initiation, it need be present in only trace amounts.
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28
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85088078181
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note
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n = 128).
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29
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0001136451
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Full details are given in the Supporting Information. Ligands of this type have been prepared previously: Parks, J. E.; Holm, R. H. Inorg. Chem. 1968, 7, 1408.
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(1968)
Inorg. Chem.
, vol.7
, pp. 1408
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Parks, J.E.1
Holm, R.H.2
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31
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84970554539
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(b) Healy, P. C.; Bendall, M. R.; Doddrell, D. M.; Skelton, B. W.; White, A. H. Aust. J. Chem. 1979, 32, 727.
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(1979)
Aust. J. Chem.
, vol.32
, pp. 727
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Healy, P.C.1
Bendall, M.R.2
Doddrell, D.M.3
Skelton, B.W.4
White, A.H.5
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33
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5244315203
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note
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w = 0.037, error of fit = 1.15, max Δ/σ = 0.24.
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34
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85088078927
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note
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2Ni: C, 54.67; H, 6.64; N, 4.40. Found: C, 54.38; H, 6.74; N, 4.29.
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35
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5244350521
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note
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f = 155 J/g.
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