Abstract
The solid-state circular dichroism (CD) of a 4-[2-(methylphenyl)ethynyl]benzoic acid/amine supramolecular organic fluorophore can be controlled by changing the position of the methyl substituent of the methylphenylethynyl unit on the achiral 4-[2-(methylphenyl)ethynyl]benzoic acid component molecule, instead of changing the chirality of the chiral amine component molecule.
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