Litcius/Paper detail

Chiroptical Enhancement of Chiral Dicarboxylic Acids from Confinement in a Stereodynamic Supramolecular Cage

Federico Begato, Roberto Penasa, Giulia Licini, Cristiano Zonta

2022ACS Sensors32 citationsDOIOpen Access PDF

Abstract

The fundamental implications that chirality has in science and technology require continuous efforts for the development of fast, economic, and reliable quantitative methods for enantiopurity assessment. Among the different analytical approaches, chiroptical techniques in combination with supramolecular methodologies have shown promising results in terms of both costs and time analysis. In this article, a tris(2-pyridylmethyl)amines (TPMA)-based supramolecular cage is able to amplify the circular dichroism (CD) signal of a series of chiral dicarboxylic acids also in the presence of a complex mixture. This feature has been used to quantify tartaric acid in wines and to discriminate different matrixes using principal component analysis (PCA) of the raw CD data.

Topics & Concepts

Supramolecular chemistryCircular dichroismChirality (physics)Supramolecular chiralityChemistryDicarboxylic acidOptical rotationTartaric acidCombinatorial chemistryStereochemistryOrganic chemistryMoleculePhysicsChiral symmetryQuantum mechanicsCitric acidQuarkNambu–Jona-Lasinio modelMolecular spectroscopy and chiralityPhotoreceptor and optogenetics researchAnalytical Chemistry and Chromatography