トリアジン-ベンゼン相互作用による超分子共聚化の複雑さを解明する
Hao Su1, Stef A H Jansen1, Tobias Schnitzer1
1Laboratory of Macromolecular and Organic Chemistry and Institute for Complex Molecular Systems (ICMS), Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
Journal of the American Chemical Society
|October 6, 2021
まとめ
この研究は,トリアジン (T) とベンゼン (B) モノメアの温度制御された超分子共聚化を明らかにした. 冷却により,BがTホモポリマーに挿入され,調整可能なマイクロ構造を持つ交互のコポリマーを形成します.
科学分野:
- 超分子化学
- ポリマー科学
- 材料科学
背景:
- 超分子共ポリマーには 複雑な機能的な分子システムがあります
- コポリマー組成とマイクロ構造をビルディングブロックの相互作用で制御することは困難です.
研究 の 目的:
- 温度に依存する2つのキラルモノメアの超分子共聚化を調査する.
- 構造の変化がコポリマーの性質にどのように影響するかを理解する.
- コポリマー形成のメカニズムを解明する.
主な方法:
- トリアジン- (T) とベンゼン- (B) ベースのモノメアの均質化.
- スペクトル分析
- 理論的なシミュレーションです
- 温度制御による自己組み立て
主要な成果:
- TのホモポリマーはBよりも安定性が高い.
- Tは高温でホモポリマーを形成する.
- 冷却すると,BはTホモポリマーに間接し,10°Cで約80%の交互結合を持つコポリマーを形成する.
- TとBコアの間の好ましいヘテロ相互作用は,より低い温度で交互のコポリマー形成を促します.
結論:
- 温度に依存する新種の超分子共聚化メカニズムが発見された.
- この研究では,温度によるコポリマーの微細構造の制御が示されています.
- 温度に反応するコポリマーマイクロ構造を明らかにする方法が提案された.
関連する概念動画
Ziegler–Natta Chain-Growth Polymerization: Overview
3.5K
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...
3.5K
Characteristics and Nomenclature of Copolymers
2.9K
Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
2.9K
Step-Growth Polymerization: Overview
3.8K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
Many natural and synthetic polymers are produced by...
3.8K
Cationic Chain-Growth Polymerization: Mechanism
2.5K
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...
2.5K
Cycloaddition Reactions: MO Requirements for Thermal Activation
3.8K
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
3.8K
Radical Chain-Growth Polymerization: Overview
2.8K
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...
2.8K


