comes from a Greek word that means "the hand." Any pairs of geometric figures or groups of points hold the chirality if they are mirror images of each other but cannot be superimposed. [1] These chiral molecules are also named "enantiomers," which can have the same energy levels with different handedness. In zoology [2,3] and botany, [4] chirality plays a substantial role in coloration. Moreover, it is crucial for enantiomer's separation and detection in pesticides, drugs, and amino acids in living organisms. For example, in pesticides, several weed killers contain dichlorprop and mecoprop molecules, where one handedness is herbicide and the other is inactive. [5] Likewise, in the pharmaceutical industry, one enantiomer of the drug, namely thalidomide, is used as relief medicine in pregnant women for morning sickness, but the other enantiomer can cause serious birth deficiencies in children. There are several other examples like levodopa (used to treat Parkinson's disease, but its other enantiomer can lead to severe chronic bacterial infections), ketamine (commonly used anesthetic whose mirror image creates hallucinations), naproxen (used as an anti-inflammatory drug but the mirror image causes liver poisoning), etc. [6][7][8][9] Additionally, all the amino acids, the building blocks of the proteins, are chiral.Left-handed circularly polarized (LCP) light and right-handed circularly polarized (RCP) light have distinct spectral responses, which are regarded as chiroptical effects. [10,11] Examples include optical activity and circular dichroism (CD) or asymmetric transmission (AT). [1,12] Optical activity can rotate the plane of linearly polarized (LP) light (a combination of LCP and RCP).