在由C1-对称CGC催化剂中心介导的烯聚合过程中的立体化学控制机制
Alessandro Motta1, Ignazio L Fragalà, Tobin J Marks
1Dipartimento di Scienze Chimiche, Università di Catania, and INSTM, UdR Catania, Viale A. Doria 6, 95125 Catania, Italy.
Journal of the American Chemical Society
|May 22, 2007
概括
这项关于olefin聚合物的研究表明,虽然 counterions 影响催化剂活性,但它们不会显著改变聚合物立体化学. 计算模型简化了分析,显示了固态因子主导着等离子聚合物形成的单体链.
科学领域:
- 有机金属化学 有机金属化学
- 聚合物科学 聚合物科学
- 计算化学的计算化学
背景情况:
- 约束几何学催化剂 (CGCs) 在烯聚合过程中至关重要.
- 了解聚合过程中的立体化学控制对于定制聚合物特性至关重要.
研究的目的:
- 用C1-对称约束几何学催化剂分析olefin聚合物的立体化学方面.
- 研究共催化剂/对催化剂和溶解对催化剂激活和单体插入的影响.
主要方法:
- 密度函数理论 (DFT) 的计算被用来研究催化剂激活和离子对分离的能量.
- 为乙烯和烯插入反应生成了计算热力学配置文件.
- 系统评估了 counterions 和 solvation 环境的影响.
主要成果:
- 催化剂激活能量与实验数据保持一致.
- 对比影响整体催化活性,但不显著影响聚合物微动力或链接立体化学.
- 绝缘效应,特别是来自不断增长的聚合物链,主要决定区域选择,并在单体插入过程中有利于同位态丰富.
结论:
- "裸体阴离子"模型在计算上是合理的,用于分析单体链接.
- 立体相互作用是这种催化系统中立体化学控制的主要驱动因素.
- 这些发现为设计特定聚合物微结构的催化剂提供了洞察力.
相关概念视频
Free-Radical Chain Reaction and Polymerization of Alkenes
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
Polymer Classification: Stereospecificity
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
Cationic Chain-Growth Polymerization: Mechanism
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Ziegler–Natta Chain-Growth Polymerization: Overview
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta catalyst, high molecular...
Olefin Metathesis Polymerization: Overview
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...


