Wahab Alexandra, Gershoni-Poranne Renana
Laboratory for Organic Chemistry, Department of Chemistry and Applied Biosciences, ETH Zurich, Zurich 8093, Switzerland.
Schulich Faculty of Chemistry and the Resnick Sustainability Center for Catalysis, Technion - Israel Institute of Technology, Haifa 32000, Israel.
J Org Chem. 2025 Sep 12;90(36):12667-12677. doi: 10.1021/acs.joc.5c01401. Epub 2025 Aug 29.
Pyrene is a central building block in organic materials chemistry, valued for its rigid aromatic core, high fluorescence, and rich capacity for structural elaboration. However, the fundamental relationship between its annelation pattern and resulting electronic properties remains underexplored. In this work, we present a comprehensive computational study of 4,766 pyrene-based polybenzenoid hydrocarbons from the COMPAS-3D data set. By systematically categorizing annelation patterns based on the positions of fused benzene rings, we uncover clear structure-property trends governing key electronic parameters, including molecular orbital energies and oxidation and reduction potentials. We find that annelations at different positions exert different effects, which combine additively, and that these trends correlate with the distribution of fixed versus migrating Clar sextets. We further show that extended linear annelation can dominate electronic behavior, superseding local pyrene effects. Additionally, we evaluate the effect of torsional strain, revealing a clear link between annelation patterns and thermodynamic molecular destabilization. These insights provide a framework for the rational design of functional pyrene-based molecules.
芘是有机材料化学中的核心构建单元,因其刚性芳香核、高荧光性以及丰富的结构修饰能力而受到重视。然而,其稠合模式与所得电子性质之间的基本关系仍未得到充分探索。在这项工作中,我们对来自COMPAS - 3D数据集的4766种基于芘的多苯并芳烃进行了全面的计算研究。通过基于稠合苯环的位置系统地对稠合模式进行分类,我们揭示了控制关键电子参数(包括分子轨道能量以及氧化和还原电位)的清晰的结构 - 性质趋势。我们发现不同位置的稠合会产生不同的影响,这些影响具有加和性,并且这些趋势与固定和迁移的克莱尔六隅体的分布相关。我们进一步表明,扩展的线性稠合可以主导电子行为,取代局部芘效应。此外,我们评估了扭转应变的影响,揭示了稠合模式与热力学分子不稳定之间的明确联系。这些见解为基于芘的功能分子的合理设计提供了一个框架。