共聚物
战术性
聚合
高分子化学
单体
材料科学
聚乙烯
活性聚合
1-己烯
链式转移
配位聚合
聚合物
自由基聚合
复合材料
作者
Mohammad Hossein Jandaghian,Ahmad Soleimannezhad,Saeid Ahmadjo,Seyed Mohammad Mahdi Mortazavi,Mostafa Ahmadi
标识
DOI:10.1021/acs.iecr.7b05339
摘要
Understanding from the underlying mechanism of chain shuttling polymerization (CSP) is limited due to scarceness of successful reports and incompetence of traditional characterization techniques to distinguish blocky structures. Here, a simple synthesis approach for production of an isotactic poly(1-hexene)/branched polyethylene multiblock copolymer from a 1-hexene monomer is presented. Resulting copolymers can be easily characterized because of their solubility in most organic solvents. This novel blocky architecture is synthesized using ansa -ethylenebis(1-η 5 -indenyl)zirconium dichloride and α-diimine nickel(II) bromide catalysts. While the former participates in 1,2-enchainment of monomers and produces amorphous segments, the latter forms methylene sequences through chain walking reaction. A quasi-living polymerization is established by reversible transfer of growing chains between catalyst components, as manifested by narrowing molecular weight distribution. 13 C NMR analysis confirms that the blocky structure can be tuned by adjusting polymerization conditions. Decrease of the crystallizable methylene sequence in the presence of CSA leads to a significant transparency of the product.
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