Well-defined transition metal complexes with phosphorus and nitrogen ligands for 1,3-dienes polymerization

被引:178
作者
Ricci, Giovanni [1 ]
Sommazzi, Anna [2 ]
Masi, Francesco [3 ]
Ricci, Marco [2 ]
Boglia, Aldo [1 ]
Leone, Giuseppe [1 ]
机构
[1] CNR, ISMAC, I-20133 Milan, Italy
[2] Eni SpA, Res Ctr Nonconvent Energies, Ist Eni Donegani, I-28100 Novara, Italy
[3] Polimeri Europa, I-20097 San Donato Milanese, Italy
关键词
Transition metal catalysts; 1,3-Dienes polymerization; Chemoselectivity; Stereoselectivity; Polybutadiene; Polyisoprene; Polypentadiene; Cobalt; Iron; Chromium; Titanium; Nickel; Phosphorus ligands; Nitrogen ligands; CO-CS2 CATALYST SYSTEM; BUTADIENE-ISOPRENE COPOLYMERIZATION; ALLYL-INSERTION MECHANISM; BOND FORMATION REACTION; NATTA TYPE CATALYSTS; X-RAY-DIFFRACTION; CONJUGATED DIENES; CRYSTAL-STRUCTURE; SYNDIOTACTIC 1,2-POLYBUTADIENE; STEREOSPECIFIC CATALYST;
D O I
10.1016/j.ccr.2009.09.023
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This article provides an overview on recent progress in the polymerization of 1,3-dienes catalyzed by transition metal complexes with phosphorus and nitrogen ligands. Polymers having different microstructures (cis-1,4: 1,2; mixed cis-1,411,2) and tacticity (iso- or syndiotactic) were obtained from various 1,3-dienes (1,3-butadiene. isoprene, 1,3-pentadienes, 1,3-hexadienes) depending on the catalyst used, clearly suggesting that the catalyst structure (i.e. metal nature, type of ligand) strongly affects the polymerization chemo- and stereoselectivity. However, as indicated by the results obtained in the polymerization of substituted butadienes, a fundamental role in determining the selectivity is also played by the type of monomer: polymers with different structure, some of them completely new, were obtained from different monomers with the same catalyst. All these observations permitted to confirm, and in some cases to improve, the knowledge on the diene polymerization mechanism. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:661 / 676
页数:16
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