对于可重复使用的粘合剂,3-甲基亚提丁的阳离子逆化
Pinxian Gao1, Weishu Yang1, Weixuan Lai1
1School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, P. R. China. haibiny@gdut.edu.cn.
概括
研究人员使用3 - 甲基乙提丁和硫开发了新的高硫聚硫化物. 这些氨基功能化聚合物形成动态网络,并作为有效的,可重复使用的木材粘合剂.
科学领域:
- 聚合物化学 聚合物化学
- 材料科学 材料科学 材料科学
- 有机化学 有机化学
背景情况:
- 元素硫 (S8) 是一个丰富且廉价的资源.
- 紧张的循环单体可以经历环开放聚合.
- 开发具有动态性质的功能性聚合物具有显著的兴趣.
研究的目的:
- 为了合成新型高硫多硫化物.
- 为了探索3 - 甲基亚提丁与元素硫的共聚合.
- 研究由此产生的聚合物的特性和应用.
主要方法:
- 阳离子聚合途径 阳离子聚合途径.
- 在120°C时,3-甲基乙丁与元素硫的共聚合.
- 聚合物结构和性质的表征.
主要成果:
- 成功的共聚合产生了具有氨基功能的高硫聚硫化物.
- 通过异环环的二次胺启动的S8环开放的演示.
- 形成动态的硫-硫 (S-S) 网络.
- 合成材料作为可重复使用的木材粘合剂的有效应用.
结论:
- 3-甲基亚提丁可以通过阴离子通路与元素硫共聚合.
- 由此产生的多硫化物具有动态的S-S网络和氨基功能.
- 这些新材料有望成为可持续和可重复使用的木材粘合剂.
相关概念视频
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
2.3K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.3K
Anionic Chain-Growth Polymerization: Overview
2.7K
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,...
2.7K
Olefin Metathesis Polymerization: Overview
2.7K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
2.7K
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
3.3K
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
3.3K
Anionic Chain-Growth Polymerization: Mechanism
2.6K
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...
2.6K
Cationic Chain-Growth Polymerization: Mechanism
3.0K
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...
3.0K


