Control of solid-state chiral optical properties of a chiral supramolecular organic fluorophore consisting of 1-pyrenesulfonic acid and chiral amine molecules

The solid-state chiral optical properties of a 1-pyrenesulfonic acid/amine supramolecular organic fluorophore could be controlled by changing the type of the aromatic ring and not the chirality of the chiral amine component molecule in the solid state.