一种超分子的Janus高分支聚合物及其光响应自组装的囊泡具有狭窄的尺寸分布
Yong Liu1, Chunyang Yu, Haibao Jin
1School of Chemistry and Chemical Engineering, State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, PR China.
Journal of the American Chemical Society
|March 8, 2013
概括
研究人员使用主机-客户互动创建了一个Janus超分支聚合物. 这种新型的两性聚合物自组装成可逆囊泡,可以形成合晶体.
科学领域:
- 聚合物化学 聚合物化学
- 超分子化学 超分子化学
- 材料科学 材料科学 材料科学
背景情况:
- 由于其独特的表面化学成分,雅努斯粒子提供了独特的特性.
- 超分子聚合物使动态和响应性材料组装成为可能.
- 超分支聚合物为先进材料提供复杂的架构.
研究的目的:
- 通过非共价宿主-客人相互作用合成一种新的Janus高分支聚合物.
- 为了研究Janus超分支聚合物的自我组装行为,使其变成囊泡.
- 探索自我组装结构的响应刺激的拆卸和聚合.
主要方法:
- 合成具有特定末端组的疏水性和疏水性高分支聚合物 (阿兹本和环氧德克斯).
- 聚合物的非共价合通过亚博烯/环氧素宿主-客体相互作用.
- 自己组装成单层双层囊泡的特征.
- 针对可逆拆卸的紫外线照射研究.
- 冷干燥用于聚合到密集的阵列中.
- 散射粒子动力学模拟用于机制和结构阐明.
主要成果:
- 通过特定的AZO/CD相互作用成功构建了Janus超分支聚合物.
- 自组装成单双层囊泡,尺寸分布受控.
- 在紫外线照射后,由于亚博异构化,囊泡的可逆分解.
- 在冷干燥条件下形成类似合晶体的阵列.
- 模拟揭示了囊泡自我组装和双层结构的动态和机制.
结论:
- 合成了一种新的Janus高分支聚合物,并证明了自我组装成响应的囊泡.
- 两性质和宿主-客人相互作用是观察到的自我组装和拆卸的关键.
- 该研究提供了对具有可调节性质的先进超分子材料设计的见解.
相关概念视频
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,...
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...
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.
Anionic Chain-Growth Polymerization: Overview
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
Pinching-off of Coated Vesicles
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...


