Abstract

Chirality conformational arrangements is a geometric property describing objects that are non superimposable on their mirror images, a phenomenon known as broken mirror symmetry. In molecular science, this results in two distinct mirror image forms called enantiomers, often labelled as RS or LD, which are right-handed and left handed versions of the same molecule. The functional significance of chirality arises from how these specific handednesses interact at chiral interfaces or with chiral light, enabling highly precise molecular analysis and offering great potential for biomedical applications.