1,2-二甲醇衍生动态,共价材料:合作自组装和可逆交叉连接
Xiangyi Zhang1, Robert M Waymouth1
1Department of Chemistry, Stanford University , Stanford, California 94305, United States.
Journal of the American Chemical Society
|March 1, 2017
概括
使用dithiolane聚合物创建了响应性的水凝. 狄奥兰的类型显著影响水凝的特性,使可调节的动态和自愈材料从块共聚物中产生.
科学领域:
- 聚合物化学
- 材料科学
- 超分子化学
背景情况:
- 含有丁醇的聚合物为动态和响应性材料提供了途径.
- 用聚乙烯氧化物和聚碳酸合成了ABAtriblock共聚物.
- 在聚碳酸块中加入了悬挂式1,2-dithiolane功能.
研究的目的:
- 为了研究dithiolane功能化的ABAtriblock共聚物的自组和凝行为.
- 阐明醇诱导的环开聚合和交联的机制.
- 为了了解dithiolane结构如何影响水凝的特性.
主要方法:
- 两块共聚物的合成和表征.
- 用于微粒结构分析的小角度X射线散射 (SAXS).
- 用于研究凝和机械性能的风学测量.
- 对二醇环开放聚合物的动力学和热力学研究.
主要成果:
- 两块共聚物在水溶液中自组成桥梁式花.
- 添加硫醇会触发二醇环开放聚合,导致交联和凝形成.
- 来自甲基酸的水凝具有动态,自我愈合的特性.
- 来自脂酸的水凝是刚性,弹性和脆性的.
- 显著不同的水凝特性与特定的dithiolane的环开聚合的热力学和动力学有关.
结论:
- 1,2-dithiolane的功能结构决定了产生的水凝的动态和机械特性.
- 具有狄奥兰基的ABA三环共聚物为设计可调节,响应的水凝提供了多功能平台.
- 结合不同的迪醇单体,可以精确控制水凝特性,从高度动态到刚性材料.
相关概念视频
Assembly of Cytoskeletal Filaments
28.1K
Cytoskeletal filaments are polymeric forms of smaller protein subunits. However, individual cytoskeletal filaments may easily disassemble or associate with other similar filaments to form rigid structures. Microfilaments, made of actin monomers, rely on actin-binding proteins to form bundles and create networks of individual actin filaments. Microtubules rely on microtubule-associated proteins (MAPs) to form sturdy cylindrical structures. However, the proteins involved in forming complex...
28.1K
Covalent Bonds
166.7K
Overview
166.7K
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
13.4K
The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.
13.4K
β-Dicarbonyl Compounds via Crossed Claisen Condensations
3.9K
Crossed Claisen condensations are base-promoted reactions between two different ester molecules producing β-dicarbonyl compounds. The reaction involving esters, with both containing α hydrogen, results in a mixture of four different products that are difficult to isolate. This reduces the synthetic utility of the reaction.
3.9K


