关于Ni(dppe) Cl(2) 催化链增长聚合物的机制研究:关于确定速率的还原性消除的证据
1Department of Chemistry and Macromolecular Science and Engineering Program, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 48109-1055, USA.
Journal of the American Chemical Society
|October 29, 2009
概括
这项研究研究了催化链增长聚合机制. 减少性消除被确定为对烯和烯单体的速率决定性步骤,而LiCl没有显示任何影响.
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
- 催化剂是一种催化剂.
背景情况:
- 催化交叉合反应在聚合物合成中至关重要.
- 了解聚合机制对于控制聚合物特性至关重要.
研究的目的:
- 阐明特定的烯和烯单体的链增长聚合机制.
- 为了确定速度决定的步骤和催化剂和单体度的作用.
主要方法:
- 使用现场红外光谱和气体染色学进行速率研究.
- 采用 (31) P 核磁共振光谱来表征有反应性的有机金属中间体.
- 研究了LiCl添加剂对聚合动学的影响.
主要成果:
- 这两种聚合都显示出第一阶依赖催化剂度和零阶依赖单体度.
- 识别了非对称的Ni (II) - 双和Ni (II) - 双烯复合体作为静止状态.
- 减少性淘汰被确定为两个单体的速率决定性步骤.
结论:
- 这些发现提供了对Ni(dppe) Cl(2) -催化链增长聚合的机理性见解.
- 减少性消除是控制聚合率的关键步骤.
- LiCl不会影响速度决定步骤或分子量分布.
相关概念视频
Radical Chain-Growth Polymerization: Mechanism
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this species into the...
Radical Chain-Growth Polymerization: Overview
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
Anionic Chain-Growth Polymerization: Mechanism
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael acceptor.
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...
Radical Chain-Growth Polymerization: Chain Branching
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...


