Chiral 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...Chiral 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-stacking interactions.The extended π 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 g_(lum) values relative to the assemblies formed by the dicyanostilbene compounds.Overall,this study provides valuable insights into the relationship between-conjugation length and the circularly polarized luminescent performance of π-conjugatedsupramolecularassemblies.展开更多
基金supported by International Partnership Program of the Chinese Academy of Sciences(Grant No.123GJHZ2022064MI)the Collaborative Innovation Program of Hefei Science Center,CAS(No.2022HSC-CIP014)+1 种基金the Fundamental Research Funds for the Central Universities(YD2060002036)the Hospital Level Project of Shanghai Sixth People's Hospital in 2020(DY2020017).
文摘Chiral 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-stacking interactions.The extended π 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 g_(lum) values relative to the assemblies formed by the dicyanostilbene compounds.Overall,this study provides valuable insights into the relationship between-conjugation length and the circularly polarized luminescent performance of π-conjugatedsupramolecularassemblies.
