# Principles of enantio-selective excitation in three-wave mixing spectroscopy of chiral molecules

## TL;DR

This paper analyzes the principles of three-wave mixing spectroscopy for chiral molecules, identifying optimal polarization conditions and phase regimes for enantio-selective excitation, and clarifies previous misconceptions in the field.

## Contribution

It provides a theoretical framework for enantio-selective excitation using three-wave mixing, highlighting the necessity of three orthogonal polarizations and distinguishing different dynamical regimes.

## Key findings

- Three orthogonal polarizations are required for enantio-selective excitation.
- Two dynamical regimes exist, corresponding to different phase conditions.
- Current excitation schemes are near optimal for C1 symmetry molecules.

## Abstract

Three-wave mixing spectroscopy of chiral molecules, which exist in left-handed and right-handed conformations, allows for enantio-selective population transfer despite random orientation of the molecules. This is based on constructive interference of the three-photon pathways for one enantiomer and destructive one for the other. We prove here that three mutually orthogonal polarization directions are required to this end. Two different dynamical regimes exist to realize enantio-selective population transfer, and we show that they correspond to different phase conditions in the three-wave mixing. We find the excitation scheme used in current rotational three-wave mixing experiments of chiral molecules with $C_1$ symmetry to be close to optimal and discuss prospects for ro-vibrational three-wave mixing experiments of axially chiral molecules. Our comprehensive study allows us to clarify earlier misconceptions in the literature.