# Tuning the Inter-Chromophore Electronic Coupling in Perylene Diimide Dimers with Rigid Covalent Linkers

## TL;DR

This paper presents a new strategy for tuning electronic coupling in perylene diimide dimers using rigid covalent linkers, which could improve organic optoelectronic materials.

## Contribution

A new molecular design strategy for tuning inter-chromophore electronic coupling using rigid covalent linkers is proposed.

## Key findings

- Rigid linking cores ensure minimal structural relaxation between S0 and S1 states.
- Saddle-shaped linkers allow tuning of dihedral and slipping angles to control electronic coupling.
- The method enables |JCoul| values ranging from 0 to 1000 cm−1.

## Abstract

The organic multi-chromophore system has been increasingly attractive due to the potential optoelectronic applications. The inter-chromophore electronic coupling (EC), i.e., JCoul and JCT, plays a critical role in determining the relaxation path of the excited state. However, the molecular designing strategy for effective tuning of inter-chromophore EC is still challenging. In this computational work, we designed a series of perylene diimides (PDI) covalent dimers with rigid linking cores containing thiophene (Th) or phenyl (Ph) fragments and performed corresponding theoretical investigation to analyze the inter-PDI electronic coupling. Vibrational analysis indicated that the minimized excited state structural relaxation (ES-SR) can ensure the rigid inter-PDI geometry pre-defined by the topological characteristic of linking cores, leading to comparable |JCoul| on S0 and S1 states. The saddle-shaped linking cores allow collaborative tuning of inter-PDI dihedral (α) and slipping (θ) angles, leading to effective tuning of inter-PDI |JCoul| = 0–1000 cm−1. Our work provides a new molecular designing strategy for effective tuning of inter-chromophore EC for organic chromophores. By using a rigid inter-chromophore structure, the ignorable ES-SR allows simplified molecular designing without considering the plausible geometric difference between S1 and S0 states, which might be useful for future applications in organic optoelectronics.