Control of the Solid‐State Chiral Optical Properties of a Supramolecular Organic Fluorophore Containing 4‐(2‐Arylethynyl)‐Benzoic Acid

Abstract

The solid-state chiral optical properties of a 4-(2-arylethynyl)-benzoic acid/amine supramolecular organic fluorophore can be controlled by changing the arylethynyl group of the achiral 4-(2-arylethynyl)-benzoic acid component molecule rather than the chirality of the amine component molecule.