Synthesis of polyethylene containing a terminal p-methylstyrene group:: Metallocene-mediated ethylene polymerization with a consecutive chain transfer reaction to p-methylstyrene and hydrogen

被引:61
作者
Dong, JY [1 ]
Chung, TC [1 ]
机构
[1] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
关键词
D O I
10.1021/ma011622n
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This paper discusses a novel polymerization process for preparing polyethylene having a terminal p-methylstyrene (p-MS) group. The chemistry involves metallocene-mediated ethylene polymerization in the presence of p-MS and hydrogen. Apparently, the reaction mechanism, including the copolymerization and chain transfer reactions, can be controlled with a favorable combination of metallocene catalyst and hydrogen concentration. Under some specific reaction conditions, the Cp2ZrCl2/MAO catalyst selectively forms PE with a terminal p-MS terminal group (PE-t-p-MS) via a consecutive chain transfer reaction to p-MS and then hydrogen. The catalyst activity increases with the hydrogen concentration, and the polymer molecular weight is inversely proportional to the p-MS concentration. In contrast, [C5Me4((SiMe2NBu)-Bu-t)]TiCl2/MAO initiates a copolymerization reaction between ethylene and p-MS, and hydrogen has little effect on the catalyst activity. The terminal p-MS unit at the PE chain end is a valuable reactive group that can be metalated to form a stable polymeric anion, which can be used to prepare functionalized PE polymers containing a polar terminal group or diblock copolymers.
引用
收藏
页码:1622 / 1631
页数:10
相关论文
共 41 条
[21]   Organolanthanide-mediated silanolytic chain transfer processes. Scope and mechanism of single reactor catalytic routes to silapolyolefins [J].
Koo, K ;
Fu, PF ;
Marks, TJ .
MACROMOLECULES, 1999, 32 (04) :981-988
[22]   Silanolytic chain transfer in Ziegler-Natta catalysis. Organotitanium-mediated formation of new silapolyolefins and polyolefin architectures [J].
Koo, KM ;
Marks, TJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (16) :4019-4020
[23]   SYNDIOTACTIC SPECIFIC POLYMERIZATION OF STYRENE - DRIVING ENERGY OF THE STERIC CONTROL AND REACTION-MECHANISM [J].
LONGO, P ;
PROTO, A ;
ZAMBELLI, A .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 1995, 196 (09) :3015-3029
[24]  
LONGO P, 1990, MAKROMOL CHEM, V191, P2387
[25]   Synthesis of long: Chain branched polypropylene with relatively well-defined molecular structure [J].
Lu, B ;
Chung, TC .
MACROMOLECULES, 1999, 32 (25) :8678-8680
[26]   Synthesis of new polyolefin elastomers, poly(ethylene-ter-propylene-ter-p-methylstyrene) and poly(ethylene-ter-1-octene-ter-p-methylstyrene), using metallocene catalysts with constrained ligand geometry [J].
Lu, HL ;
Hong, S ;
Chung, TC .
MACROMOLECULES, 1998, 31 (07) :2028-2034
[27]  
Lu HL, 1999, J POLYM SCI POL CHEM, V37, P2795, DOI 10.1002/(SICI)1099-0518(19990801)37:15<2795::AID-POLA14>3.0.CO
[28]  
2-L
[29]   Zirconocene-based catalysts for the ethylene-styrene copolymerization: Reactivity ratios and reaction mechanism [J].
Oliva, L ;
Longo, P ;
Izzo, L ;
DiSerio, M .
MACROMOLECULES, 1997, 30 (19) :5616-5619
[30]   REGIOSPECIFICITY OF ETHYLENE-STYRENE COPOLYMERIZATION WITH A HOMOGENEOUS ZIRCONOCENE CATALYST [J].
OLIVA, L ;
CAPORASO, L ;
PELLECCHIA, C ;
ZAMBELLI, A .
MACROMOLECULES, 1995, 28 (13) :4665-4667