来自相同的前体的不同结合聚合物的制备,其特点是具有互补的电子特性
Marco Carlotti1,2,3, Tommaso Losi4, Francesco De Boni5
1Dipartimento di Chimica e Chimica Industriale, University of Pisa Via G. Moruzzi 13 56124 Pisa Italy marco.carlotti@iit.it marco.carlotti@unipi.it.
概括
研究人员开发了一种多功能聚合物前体,可转化为两种不同的合聚合物,使得从单一材料中创建具有不同电子特性的有机电子设备成为可能.
科学领域:
- 有机电子学有机电子学
- 聚合物化学 聚合物化学
- 材料科学是一种材料科学.
背景情况:
- 开发具有空间定义电子特性的有机半导体是先进设备的关键.
- 目前的方法通常需要复杂的多步合成或设备制造.
研究的目的:
- 为推出一种新的,高度可加工的聚合物前体.
- 证明其能够产生两种具有互补电荷传输特性 (电子或孔传输) 的不同合聚合物的能力.
- 探索其在制造功能性有机电子元件中的应用.
主要方法:
- 基于功能化二甲单元的新型聚合物前体的合成.
- 前体薄膜的固态转化成两个不同的结合聚合物.
- 对前体和由此产生的聚合物的化学和电子特性进行表征.
主要成果:
- 聚合物前体能够成功地产生含有乙烯和甲单元的高分子合聚合物,而无侧链.
- 前体的薄膜可以转化为单层,具有不同的化学和电子区域.
- 在电色表面和有机场效应晶体管中应用的潜力已被证明.
结论:
- 这一策略为从单一前体中创建多功能有机半导体薄膜提供了一个简单的途径.
- 开发的材料有望简化复杂的有机电子设备的制造.
相关概念视频
Characteristics and Nomenclature of Copolymers
2.5K
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...
2.5K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
1.9K
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...
1.9K
Anionic Chain-Growth Polymerization: Overview
2.1K
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,...
2.1K
Olefin Metathesis Polymerization: Overview
2.1K
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...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.1K
Polymers
35.8K
The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the...
35.8K
Thermal and Photochemical Electrocyclic Reactions: Overview
2.3K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.3K


