Affiliation:
1. Key Laboratory of Precision and Intelligent Chemistry, Department of Polymer Science and Engineering University of Science and Technology of China Hefei Anhui 230026 China
2. Department of Thoracic Surgery Shanghai Jiao Tong University Affiliated Sixth People's Hospital Shanghai 200233 China
Abstract
Comprehensive SummaryChiral supramolecular assembly of π‐conjugated luminophores provides a promising avenue for enhancing circularly polarized luminescence. In this study, we shed light on the impact of π‐conjugation length on circularly polarized luminescent performance of the resulting supramolecular assemblies, by designing a tetra‐cyanostilbene monomeric compound alongside two dicyanostilbene control compounds. These cyanostilbene‐based compounds possess the ability to form chiral supramolecular polymers in toluene, driven by a synergistic combination of intermolecular hydrogen bonding and π–π stacking interactions. The extended π‐aromatic skeleton brings bathochromic‐shifted fluorescence and enhanced intermolecular stacking capability for the tetra‐cyanostilbene compound. Consequently, chiral supramolecular assemblies formed by the tetra‐cyanostilbene compound demonstrate a remarkable two‐fold increase in glum values relative to the assemblies formed by the dicyanostilbene compounds. Overall, this study provides valuable insights into the relationship between π‐conjugation length and the circularly polarized luminescent performance of π‐conjugated supramolecular assemblies.