Chain Growth Polymerization of Isoprene and Stereoselective Isoprene鈥揝tyrene Copolymerization Promoted by an ansa-Bis(indenyl)allyl鈥揧ttrium Complex
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- 作者：Liana Annunziata ; Michel Duc ; Jean-Franc抬ois Carpentier
- 刊名：Macromolecules
- 出版年：2011
- 出版时间：September 27, 2011
- 年：2011
- 卷：44
- 期：18
- 页码：7158-7166
- 全文大小：901K
- 年卷期：v.44,no.18(September 27, 2011)
- ISSN：1520-5835
文摘
The ability of rac-[{Me2C(Ind)2}Y(1,3-(SiMe3)2C3H3)] (Ind = 9-indenyl) (1) to catalyze isoprene polymerization, either as a single-site component or in combination with an alkyl鈥搈etal as a chain transfer agent (CTA) via coordinative chain transfer polymerization (CCTP), has been investigated. Complex 1 alone catalyzes the highly 1,4-trans-stereoselective polymerization of isoprene with moderate activity. The addition of ZnEt2 provides an efficient catalytic system for the reversible CCTP of isoprene with retention of the 1,4-trans stereoselectivity. By contrast, in the presence of Mg(nBu)2, with increasing amounts of CTA, the 1,4-trans specificity gradually decreases at the advantage of the 3,4-polymer. The copolymerization between isoprene and styrene has been also studied, resulting in the formation of materials with unprecedented architecture. Simultaneous copolymerization of isoprene and styrene with 1 provides copolymers with a wide range of compositions (蠂S = 0.30鈥?.98) and a stereospecific blocky distribution of the monomers in the copolymer chain. The reactivity ratios (average values: r1,Ip = 2 and r2,St = 18) determined by NMR spectroscopy confirmed the propensity to form multiblock materials. Microstructural 13C NMR analysis showed the presence of stereoregular 1,4-trans-polyisoprene and isotactic polystyrene segments. The copolymerization via sequential monomer addition allowed the synthesis of well-defined 1,4-trans-polyisoprene-block-isotactic polystyrene, which contains two crystalline blocks. The authenticity of these new di- or multiblock copolymer materials was assessed by combined NMR, GPC, and DSC characterizations.