Water-tolerant catalyst systems for the bulk cationic polymerization of para-methylstyrene and indene

被引:5
作者
Vergnaud, Jerome [1 ]
Sarazin, Yann [1 ]
Strub, Henri [2 ]
Carpentier, Jean-Francois [1 ]
机构
[1] Univ Rennes 1, CNRS, UMR Sci Chim Rennes 6226, F-35042 Rennes, France
[2] Ctr Rech Oise, F-60550 Verneuil En Halatte, France
关键词
Catalysis; Cationic polymerization; Metal triflates; Tris(pentafluorophenyl)borane; P-METHOXYSTYRENE; AQUEOUS-MEDIA; LEWIS-ACID; EMULSION; STYRENE; TRIS(PENTAFLUOROPHENYL)BORANE; HYDROXYSTYRENE; MINIEMULSION; COPOLYMERS; YB(OTF)(3);
D O I
10.1016/j.eurpolymj.2010.01.014
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Water-tolerant catalyst systems have been investigated for the cationic oligomerization of technical-grade p-methylstyrene and indene, for the production of industrially relevant aromatic resins. Systems based on 1-p-tolylethanol and 1-indanol (ROH) as initiators, in association with Cu(OTf)(2), Bi(OTf)(3) (MT = triflate) and B(C6F5)(3) as co-initiators/catalysts, show interesting productivities at 60 degrees C under air, with as low as 0.2-1.0 mol% catalyst loading. Most of the reactions are not controlled in terms of molecular weights of the products, except for indene oligomerization by the borane catalyst where experimental M,, values match well the theoretical values, as determined by the amount of added initiator over a 5-fold range (with 2-10 mol% vs. monomer). The ROH/tris(pentafluorophenyl)borane system offers the best compromise in terms of productivity and control over the molecular weights of the oligomers, which can be manipulated by the amount of initiator and reaction temperature. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1093 / 1099
页数:7
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