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Razavi, A.; Bellia, V.; De Brauwer, Y.; Hortmann, K.; Peters, L.; Sirol, S.; Van Belle, S.; Thewalt, U. Macromol. Chem. Phys. 2004, 205, 347
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0001654716
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Gladysz, J. A. Special issue: Frontiers in Metal-Catalyzed Polymerization Chem. Rev. 2000, 100, 1167
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Gladysz, J.A.1
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Fluorenyl Containing Catalysts for Stereoselective Propylene Polymerization
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Baugh, L. S.; Canich, J. A. M., Eds.; CRC Press.
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Price, C. J.; Irwin, L. J.; Aubry, D. A.; Miller, S. A. Fluorenyl Containing Catalysts for Stereoselective Propylene Polymerization. In Stereoselective Polymerization with Single Site Catalysts; Baugh, L. S.; Canich, J. A. M., Eds.; CRC Press, 2000.
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Price, C.J.1
Irwin, L.J.2
Aubry, D.A.3
Miller, S.A.4
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11
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78149336678
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Kirillov, E.; Marquet, N.; Razavi, A.; Belia, V.; Hampel, F.; Roisnel, T.; Gladysz, J. A.; Carpentier, J.-F. Organometallics 2010, 29, 5073.
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Organometallics
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Kirillov, E.1
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14
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0000334791
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For relevant procedures, see
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For relevant procedures, see: Day, J. H. Chem. Rev. 1953, 53, 167
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Day, J.H.1
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19
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70349967084
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(Université de Rennes 1 and Total Petrochemicals Co.) EP06121181.9,Sept 25, 2006.
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Carpentier, J.-F.; Kirillov, E.; Razavi, A. (Université de Rennes 1 and Total Petrochemicals Co.) Eur. Pat. Appl. EP06121181.9,Sept 25, 2006.
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Eur. Pat. Appl.
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Carpentier, J.-F.1
Kirillov, E.2
Razavi, A.3
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20
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70349967084
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(Friedrich-Alexander Universität Erlangen-Nürnberg and Atofina Co.) EP05105162.1, June 13, 2005.
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Kirillov, E.; Gladysz, J. A.; Razavi, A. (Friedrich-Alexander Universität Erlangen-Nürnberg and Atofina Co.) Eur. Pat. Appl. EP05105162.1, June 13, 2005.
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Eur. Pat. Appl.
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Kirillov, E.1
Gladysz, J.A.2
Razavi, A.3
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21
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78751539403
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Solvent effects in the nucleophilic addition of the fluorenyl anion to sterically protected fulvenes have been noticed in our previous study; see ref 3.
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Solvent effects in the nucleophilic addition of the fluorenyl anion to sterically protected fulvenes have been noticed in our previous study; see ref 3.
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22
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78751478932
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The small amount of proligand 2c isolated was sufficient to explore its metalation and coordination onto Zr, which eventually turned out unsuccessful (vide infra). Optimization of the synthesis of this compound, e.g., using protocol D, was therefore not further investigated.
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The small amount of proligand 2c isolated was sufficient to explore its metalation and coordination onto Zr, which eventually turned out unsuccessful (vide infra). Optimization of the synthesis of this compound, e.g., using protocol D, was therefore not further investigated.
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26
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22744437750
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Irwin, L. J.; Reibenspies, J. H.; Miller, S. A. Polyhedron 2005, 24, 1314
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Polyhedron
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Irwin, L.J.1
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Miller, S.A.3
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27
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0033743203
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Drago, D.; Pregosin, P. S.; Razavi, A. Organometallics 2000, 19, 1802
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Organometallics
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Drago, D.1
Pregosin, P.S.2
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29
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78751537895
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m, isotacticity) of the isolated polymer.
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m, isotacticity) of the isolated polymer.
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30
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78751554246
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This 40:60 molar diastereomeric mixture was obtained by evaporation/crystallization of the mother liquor obtained after the isolation of anti -3a diastereomer.
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This 40:60 molar diastereomeric mixture was obtained by evaporation/crystallization of the mother liquor obtained after the isolation of anti -3a diastereomer.
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31
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66649136170
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+ through reaction with trimethylaluminium present in commercial MAO toluene solutions; see
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+ through reaction with trimethylaluminium present in commercial MAO toluene solutions; see: Busico, V.; Cipullo, R.; Pellecchia, R.; Talarico, G.; Razavi, A. Macromolecules 2009, 42, 1789
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(2009)
Macromolecules
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Busico, V.1
Cipullo, R.2
Pellecchia, R.3
Talarico, G.4
Razavi, A.5
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32
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67650388209
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Propylene polymerization promoted by discrete but multisite (pyridylamide)hafnium post-metallocenes was recently reported; see
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Propylene polymerization promoted by discrete but multisite (pyridylamide)hafnium post-metallocenes was recently reported; see: Busico, V.; Cipullo, R.; Pallecchia, R.; Rongo, L.; Talarico, G.; Macchioni, A.; Zuccaccia, C.; Froese, R. D. J.; Hustad, P. D. Macromolecules 2009, 42, 4369
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(2009)
Macromolecules
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Busico, V.1
Cipullo, R.2
Pallecchia, R.3
Rongo, L.4
Talarico, G.5
MacChioni, A.6
Zuccaccia, C.7
Froese, R.D.J.8
Hustad, P.D.9
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33
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0000105871
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-; see
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-; see: Babushkin, D. E.; Semikolenova, N. V.; Zakharov, V. A.; Tasli, E. Macromol. Chem. Phys. 2000, 201, 558
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Macromol. Chem. Phys.
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Babushkin, D.E.1
Semikolenova, N.V.2
Zakharov, V.A.3
Tasli, E.4
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34
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16244380223
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The use of diastereomeric metallocenes may lead obviously to even more complex mixtures, with a distinct behavior for each diastereomeric precursor.
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Merle, P. G.; Cheron, V.; Hagen, H.; Lutz, M.; Spek, A. L.; Deelman, B.-J.; Van Koten, G. Organometallics 2005, 24, 1620 The use of diastereomeric metallocenes may lead obviously to even more complex mixtures, with a distinct behavior for each diastereomeric precursor.
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(2005)
Organometallics
, vol.24
, pp. 1620
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Merle, P.G.1
Cheron, V.2
Hagen, H.3
Lutz, M.4
Spek, A.L.5
Deelman, B.-J.6
Van Koten, G.7
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35
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77953291355
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4] resulted in simultaneous hydride and methide abstraction, to afford silylium-metallocenium heterodicationic complexes. The latter species, being highly electrophilic, appeared to be at least 2 times more active in propylene polymerization than the corresponding metallocenium monocations; see
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4] resulted in simultaneous hydride and methide abstraction, to afford silylium-metallocenium heterodicationic complexes. The latter species, being highly electrophilic, appeared to be at least 2 times more active in propylene polymerization than the corresponding metallocenium monocations; see: Zhang, Y.; Chen, E. Y.-X. J. Organomet. Chem. 2010, 695, 1464
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Zhang, Y.1
Chen, E.Y.-X.2
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36
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78751524135
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(Atofina Co.) WO00/49029
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Razavi, A. (Atofina Co.) PCT Int. Appl. WO00/49029, 1999.
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PCT Int. Appl.
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Razavi, A.1
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