电离子和基聚合物的光控制互转换
Veronika Kottisch1, Quentin Michaudel1, Brett P Fors1
1Cornell University , Ithaca, New York 14853, United States.
Journal of the American Chemical Society
|July 27, 2017
概括
这项研究引入了一种光控制的方法,通过选择性地激活离子或基质聚合机制来精确设计聚合物结构. 这种创新允许使用不同的光波长调节聚合物序列和架构.
科学领域:
- 聚合物化学
- 摄影化学
- 材料科学
背景情况:
- 控制聚合物序列和结构对于先进的材料特性至关重要.
- 同时的聚合机制为复杂的聚合物架构提供了潜力.
- 外部刺激提供了一种调节化学反应的手段.
研究的目的:
- 开发一种用于合成可控序列和结构的聚合物的一种策略.
- 用光作为外部刺激来实现可切换的单体选择性.
- 通过光催化剂调制探索复杂的聚合物结构的设计.
主要方法:
- 采用一种结合阴离子和激素聚合的单装置.
- 使用特定波长的光来选择性地激活聚合途径.
- 调整两个光催化剂的比率以实现互补的化学控制.
主要成果:
- 基于波长选择的光诱导对单体的控制.
- 在相同的溶液条件下成功合成多种聚合物结构.
- 通过光催化剂调节来设计精细的聚合物架构的能力.
结论:
- 光作为一种强大的外部刺激,用于精确调节聚合过程.
- 开发的战略为创建定制的聚合物序列和结构提供了一个多功能平台.
- 这种方法推进了受控聚合和材料设计领域.
相关概念视频
Cationic Chain-Growth Polymerization: Mechanism
2.9K
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...
2.9K
Radical Chain-Growth Polymerization: Mechanism
3.7K
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...
3.7K
Radical Chain-Growth Polymerization: Overview
3.6K
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...
3.6K
Radical Chain-Growth Polymerization: Chain Branching
2.6K
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...
2.6K
Free-Radical Chain Reaction and Polymerization of Alkenes
10.0K
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.
10.0K
Photochemical Electrocyclic Reactions: Stereochemistry
2.3K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
2.3K


