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33745789365
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note
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g = 24.60°C.
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33745775629
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note
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17
-
-
-
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79
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33745799630
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note
-
n values vs polystyrene standards by GPC were higher than those estimated values if internal olefins were formed only by the β-hydrogen elimination. The reason for the low catalytic activity by 2 may be due to stabilization by coordination of internal olefin after the isomerization.
-
-
-
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80
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33745773229
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-
note
-
2=CHR) as the polymer chain end was observed in poly(ethylene-co-2M1P)s (2M1P: 2-methyl-l-pentene) prepared by 1 under high 2M1P concentration conditions (for the copolymer with high 2M1P content), and this clearly suggests that 2M1P insertion in the copolymerization takes place in 1,2-insertion mode, and the chain transfer in the copolymerization is due to the β-hydrogen elimination after 2,1-insertion (misinsertion): Nomura, K.; Itagaki, K., unpublished results. The result also suggests that the present HD polymerization by 1 took place in the preferred 1,2-insertion.
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note
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17 This is because use of DDMAS should be favored over CPMAS to estimate the contents quantitatively.
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33745766034
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note
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It can be assumed that there are two types of possible cross-linking in the present HD polymerization such as (i) imermolecular cross-linking (incorporation of the olefinic double bonds into the other polymer chain) and (ii) intramolecular cross-linking (incorporation of the olefinic double bonds into the same polymer chain, making large rings). The observed difference in the E′ value at the rubbery plateau for resultant poly(HD)s prepared between by the Cp*-aryloxo analogue (1) and by the Cp*-ketimide analogue (6) would be assumed to be due to the nature of the cross-linking because the E′ value at the rubbery plateau should be low if some extent of case ii accompanied, because these are not the actual network structure in the resultant polymers.
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84
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33745801273
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note
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n = 3.27, run 54). Moreover, since the E′ value at the rubbery plateau was somewhat higher than those for poly(HD)s prepared by 1 and 6 and also since the content of olefinic double bonds in the polymer was close to that by 1 under the same conditions (7a and e), these results should suggest that some extent of cyclization took place in addition to cross-linking. These results should also indicate that the selectivity was affected by both cyclopentadienyl and anionic ancillary donor ligand employed.
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85
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0032570973
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Suhm, J.; Schneider, M. J.; Mülhaupt, R. J. Mol. Catal. A 1998, 128, 215.
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Suhm, J.1
Schneider, M.J.2
Mülhaupt, R.3
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0034647240
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Zhang, S.; Piers, W. E.; Gao, X.; Parvez, M. J. Am. Chem. Soc. 2000, 122, 5499.
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J. Am. Chem. Soc.
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, pp. 5499
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Zhang, S.1
Piers, W.E.2
Gao, X.3
Parvez, M.4
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87
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33745799808
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US Patent (Sumitomo Chemical Co.) 5965758
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Nabika, M.; Nomura, K. US Patent (Sumitomo Chemical Co.) 5965758, 1999.
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(1999)
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Nabika, M.1
Nomura, K.2
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