通过在基于diketopyrrolopyrrole的合聚合物中进行战略替代来调节光电子性能
Shifan Wang1, Chen Pan2, Wenju Li2
1School of Material and Chemistry Engineering, Xuzhou University of Technology, Xuzhou 221018, China.
Langmuir : the ACS journal of surfaces and colloids
|June 9, 2025
概括
联聚合物为有机电子产品提供了具有成本效益的替代品. 这些聚合物的素工程为优化有机场效应晶体管性能和设计先进的有机半导体提供了洞察力.
科学领域:
- 材料科学 材料科学 材料科学
- 有机电子 有机电子
- 聚合物化学 聚合物化学
背景情况:
- 联聚合物是有机电子产品中化聚合物的经济有效替代品.
- 在化聚合物中对有机场效应晶体管 (OFET) 性能的优化策略尚未得到充分研究.
研究的目的:
- 为了研究分子结构和OFET性能之间的关系,在化二甲基 (DPP) 基共聚物中.
- 为了探索的结合对聚合物特性和设备性能的影响.
主要方法:
- 三种化DPP基共聚合物的合理设计和合成 (PDPP-TBT,PDPP-TBTCl和PDPP-TBTCl2).
- 有机场效应晶体管 (OFET) 的制造和表征.
- 对分子结构和电子性质的计算研究.
主要成果:
- 与PDPP-TBTCl2 (0.003 cm2 V−1 s−1) 相比,PDPP-TBTCl2 (0.003 cm2 V−1 s−1) 中的减少导致孔移动性减弱 (0.011 cm2 V−1 s−1).
- 的结合诱导了脊柱扭曲 (0-42°),破坏了聚合物平面性,降低了最高占有分子轨道 (HOMO) 能量水平 (-5.49 eV对于PDPP-TBTCl).
- 在添加时观察到增强的热稳定性.
结论:
- 分子结构,特别是含量,显著影响OFET中合聚合物的性能.
- 素工程是一种可行的策略,用于调整电子属性并增强有机半导体的热稳定性.
- 本研究提供了通过战略素修饰设计高性能有机半导体的见解.
相关概念视频
Photochemical Electrocyclic Reactions: Stereochemistry
1.9K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
1.9K
Thermal and Photochemical Electrocyclic Reactions: Overview
2.5K
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.
2.5K
Halogenation of Alkenes
16.5K
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
16.5K
ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3
6.4K
All ortho–para directors, excluding halogens, are activating groups. These groups donate electrons to the ring, making the ring carbons electron-rich. Consequently, the reactivity of the aromatic ring towards electrophilic substitution increases. For instance, the nitration of anisole is about 10,000 times faster than the nitration of benzene. The electron-donating effect of the methoxy group in anisole activates the ortho and para positions on the ring and stabilizes the corresponding...
6.4K
ortho–para-Directing Deactivators: Halogens
5.9K
Halogens are ortho–para directors. They are more electronegative than carbon. Therefore, as ring substituents, they can withdraw electrons through the inductive effect and deactivate the aromatic ring towards electrophilic substitution. Halogens also have an electron-donating resonance effect on the ring, which influences the orientation of the incoming electrophile. If an electrophile attacks at the ortho or the para position, the halogen donates electrons and stabilizes the intermediate...
5.9K
Polymer Classification: Stereospecificity
2.7K
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
2.7K


