Do Khue U, Conner Audrey V, Wheeler Steven E
Department of Chemistry, University of Georgia, Athens, Georgia 30602, United States.
J Am Chem Soc. 2025 Sep 3;147(35):32273-32286. doi: 10.1021/jacs.5c12769. Epub 2025 Aug 21.
Heteroatoms can profoundly impact the strength and preferred geometry of parallel and T-shaped interactions between aromatic systems. Understanding these heteroatom effects is vital for the rational design of everything from pharmaceuticals to asymmetric catalysts and organic materials. We first examine how the introduction of N:, NH, and C═O groups changes the shape of the relaxed interaction energy curve for the parallel-displaced benzene dimer. These heteroatom effects are shown to be (1) additive; (2) dependent primarily on the orientation of the heteroatom(s) relative to the displacement axis; and (3) driven by electrostatic effects. We then introduce a simple conceptual model to make sense of these results based on the interaction of a local dipole associated with each heteroatom with the electric field of the other aromatic system. Finally, we demonstrate how this model can be applied to complex parallel stacked dimers as well as T-shaped interactions, providing a way to make sense of heteroatom effects in π-π interactions without computations.
杂原子能够深刻影响芳香体系之间平行和T形相互作用的强度及优选几何结构。理解这些杂原子效应对于从药物到不对称催化剂以及有机材料等所有物质的合理设计至关重要。我们首先研究引入N:、NH和C═O基团如何改变平行位移苯二聚体的弛豫相互作用能曲线的形状。这些杂原子效应表现为:(1)具有加和性;(2)主要取决于杂原子相对于位移轴的取向;(3)由静电效应驱动。然后,我们引入一个简单的概念模型,基于与每个杂原子相关的局部偶极子与另一个芳香体系的电场之间的相互作用来解释这些结果。最后,我们展示了该模型如何应用于复杂的平行堆叠二聚体以及T形相互作用,提供了一种无需计算就能理解π-π相互作用中杂原子效应的方法。