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Synthesis and X-ray structure of CoCl2((PiPrPh2)2. A new highly active and stereospecific catalyst for 1,2 polymerization of conjugated dienes when used in association with MAO (Articolo in rivista)
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- Synthesis and X-ray structure of CoCl2((PiPrPh2)2. A new highly active and stereospecific catalyst for 1,2 polymerization of conjugated dienes when used in association with MAO (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ma0476083 (literal)
- Alternative label
Ricci, G.; Forni, A.; Boglia, A.; Motta, T.; Zannoni, G.; Canetti, M.; Bertini, F. (2005)
Synthesis and X-ray structure of CoCl2((PiPrPh2)2. A new highly active and stereospecific catalyst for 1,2 polymerization of conjugated dienes when used in association with MAO
in Macromolecules (Print); American Chemical Society, Washington (Stati Uniti d'America)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Ricci, G.; Forni, A.; Boglia, A.; Motta, T.; Zannoni, G.; Canetti, M.; Bertini, F. (literal)
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- IF 2005: 4.024;
SJR 2005: Materials Chemistry, Q1 (literal)
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- http://pubs.acs.org.pros.lib.unimi.it/doi/full/10.1021/ma0476083 (literal)
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- CNR-Istituto per lo Studio delle Macromolecole (ISMAC), via E. Bassini 15, 20133 Milano, Italy;
CNR-Istituto di Scienze e Tecnologie Molecolari (ISTM), via C. Golgi 19, 20133 Milano, Italy (literal)
- Titolo
- Synthesis and X-ray structure of CoCl2((PiPrPh2)2. A new highly active and stereospecific catalyst for 1,2 polymerization of conjugated dienes when used in association with MAO (literal)
- Abstract
- The new cobalt (II) phosphine complex CoCl2((PiPrPh2)2 was synthesized by reacting CoCl2 with isopropyldiphenylphosphine in ethyl alcohol as solvent. The molecular structure of the complex was determined by the X-ray diffraction method. CoCl2(PiPrPh2)2 was then used in combination with methylaluminoxane for the polymerization of 1,3-butadiene: it was found to be highly active and stereospecific for the preparation of 1,2 syndiotactic polybutadiene. The same system was also able to polymerize substituted butadienes giving highly stereoregular 1,2 polymers from E-1,3-pentadiene, 1,3-hexadiene, and 3-methyl-1,3-pentadiene. Some of these polymers are completely new and were never prepared before. (literal)
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