介绍"Ynene"转化:环扩展转化聚合导致高Cis和Syndiotactic循环聚合物的Norbornene
Soufiane S Nadif1, Tomohiro Kubo2, Stella A Gonsales1
1Center for Catalysis, Department of Chemistry, University of Florida , P.O. Box 117200, Gainesville, Florida 32611, United States.
Journal of the American Chemical Society
|May 13, 2016
概括
基酸启动诺波聚合,产生循环多聚诺波. 复合物3生产高性和联合性循环聚合物,通过先进的特征化技术得到证实.
科学领域:
- 有机金属化学
- 聚合物科学
- 催化剂
背景情况:
- 类是有机金属化学中的多功能前体.
- 氨酸转化和聚合是催化过程中的关键转化.
- 控制聚合物拓和立体化学对于材料性能至关重要.
研究的目的:
- 研究基与乙烯的反应性.
- 探索这些复合物的催化活性在norbornene聚合.
- 以循环拓学和立体选择性为重点,描述由此产生的多元化结构.
主要方法:
- 基的合成和表征.
- 与乙烯反应,形成金属基和基复合物.
- 使用基作为启动剂的诺伯聚合物.
- 聚合物特性分析,包括内在粘度,旋转半径和化时间.
主要成果:
- 基基 (1和3) 与乙烯反应,形成金属基基基基基基基基基基基基基 (4).
- 这两种复合物在室温下启动norbornene聚合.
- 复合物1产生非立体选择性聚合物,而复合物3产生高度的cis和syndiotactic循环聚合物.
- 特性数据证实了合成的多聚烯的循环拓.
结论:
- 基基作为诺波聚合物的有效启动剂.
- 连接体环境显著影响生成的多聚烯的立体选择性和拓性.
- 复合物3为高度有序的循环多聚烯提供了途径,在先进材料中具有潜在的应用.
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