Eibenberger Sandra, Doyle John, Patterson David
Harvard University, Department of Physics, 17 Oxford Street, Cambridge, Massachusetts 02138, USA.
Phys Rev Lett. 2017 Mar 24;118(12):123002. doi: 10.1103/PhysRevLett.118.123002. Epub 2017 Mar 21.
State-selective enantiomeric excess is realized using microwave-driven coherent population transfer. The method selectively promotes either R or S molecules to a higher rotational state by phase-controlled microwave pulses that drive electric-dipole allowed rotational transitions. We demonstrate the enantiomer-specific state transfer method using enantiopure samples of 1,2-propanediol. This method of state-specific enantiomeric enrichment can be applied to a large class of asymmetric, chiral molecules that can be vaporized and cooled to the point where rotationally resolved spectroscopy is possible, including molecules that rapidly racemize. The rapid chiral switching demonstrated here allows for new approaches in high-precision spectroscopic searches for parity violation in chiral molecules.
利用微波驱动的相干布居转移实现了态选择性对映体过量。该方法通过驱动电偶极允许的转动跃迁的相位控制微波脉冲,将R或S分子选择性地激发到更高的转动态。我们使用对映体纯的1,2 - 丙二醇样品展示了对映体特异性态转移方法。这种态特异性对映体富集方法可应用于一大类能够蒸发并冷却到可以进行转动分辨光谱的不对称手性分子,包括那些快速外消旋的分子。这里展示的快速手性切换为高精度光谱学研究手性分子中的宇称破缺提供了新方法。