离域电子
共轭体系
分子内力
二肽
材料科学
聚合物
接受者
芳香性
电子受体
化学物理
结合
电子
化学
光化学
分子
有机化学
肽
物理
复合材料
凝聚态物理
数学分析
生物化学
数学
量子力学
作者
Zihao Guo,Sijing Wang,Feng Ye,Jingyi Wang,Riqing Ding,Meishan Peng,Jia-Tong Li,Yidan Luan,Jiaqiang Liao
标识
DOI:10.1002/anie.202413782
摘要
Cross conjugation, though prevalent in many organic compounds, is typically considered less effective for electron delocalization compared to linear conjugation. Consequently, it is rarely used as the backbone structure for semiconducting conjugated polymers. In this study, we designed and synthesized a novel building block, TIDP, which features a central cyclic dipeptide with cross conjugation characteristics. Strong intramolecular hydrogen bonding interactions confer TIDP with a highly rigid and coplanar conformation. Importantly, theoretical calculations reveal that π electrons are well delocalized across the entire structure, despite its low aromaticity. Conjugated polymers incorporating TIDP exhibit high charge carrier mobilities, demonstrating the effective π electrons delocalization of this innovative building block. Our findings show that with rational design, cross conjugation can achieve effective π electrons delocalization, providing a valuable approach for developing high-performance conjugated polymers for organic electronic materials.
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