A facile two-step route to branched polyisoprenes via ABn-macromonomers

被引:21
|
作者
Lopez-Villanueva, Francisco-Javier [1 ]
Wurm, Frederik [1 ]
Kilbinger, Andreas F. M. [1 ]
Frey, Holger [1 ]
机构
[1] Univ Mainz, Inst Organ Chem, D-55099 Mainz, Germany
关键词
addition polymerization; anionic polymerization; branched; hydrosilylation; macromonomers; polyisoprene;
D O I
10.1002/marc.200600782
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A facile two-step synthesis for branched poly(isoprene)s (PI) based on polyaddition of AB(n)-type macromonomers is described. The synthesis of the macromonomers was achieved by anionic polymerization of isoprene and subsequent end-capping of the polymers by addition of chlorodimethylsilane to the living carbanions. This led to PI-based macromonomers with narrow polydispersity ((M) over bar (w)/(M) over bar (n) < 1.15) and molecular weights in the range of 1700 22 100 g.mol(-1). Synthesis of the branched polymers was carried out by a hydrosilylation-based polymerization of the macromonomers. Characterization via SEC, SEC-MALLS, coupled SEC-viscosimetry and H-1-NMR- spectroscopy supported the formation of branched structures, Interestingly, these branched polymers exhibited a-values that were similar to those reported for hyperbranched polymers based on AB(2)-monomers.
引用
收藏
页码:704 / 709
页数:6
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