Novel Means of Controlling
the Solid-State Circular Dichroism Property in a Supramolecular Organic
Fluorophore Comprising 4-[2-(Methylphenyl)ethynyl]benzoic Acid by
Varying the Position of the Methyl Substituent
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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