State-specific Enrichment of Chiral Conformers with Microwave Spectroscopy
arXiv:2106.05689 · doi:10.1021/acs.jpclett.8b01815
Abstract
An interesting class of molecules is that in which the molecules do not possess a stereogenic center but can become chiral due to their spatial arrangement. These molecules can be seen as chiral conformers, whose two non-superimposable forms can interconvert from one another by rotations about single bonds. Here, we show that an initially racemic mixture of chiral conformers, such as a sample of cyclohexylmethanol, CHO (CHM), can be enantiomerically enriched by performing the enantio-selective process of coherent population transfer between rotational levels. By first performing a population transfer cycle, followed by a three-wave mixing experiment, we show that an enantiomeric excess in a rotational level of choice can be achieved. This represents the first experimental demonstration of such an effect in a chiral pair of conformers, and it showcases the broad applicability of three-wave mixing not only for analytical applications but also to a wide scope of experiments of fundamental interest.
15 pages, 3 figures
References in corpus (2)
Cited by in corpus (13)
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