| Literature DB >> 32220038 |
Yantao Pang1, Anoop Thomas1, Kalaivanan Nagarajan1, Robrecht M A Vergauwe1, Kripa Joseph1, Bianca Patrahau1, Kuidong Wang1, Cyriaque Genet1, Thomas W Ebbesen1.
Abstract
It is well known that symmetry plays a key role in chemical reactivity. Here we explore its role in vibrational strong coupling (VSC) for a charge-transfer (CT) complexation reaction. By studying the trimethylated-benzene-I2 CT complex, we find that VSC induces large changes in the equilibrium constant KDA of the CT complex, reflecting modifications in the ΔG° value of the reaction. Furthermore, by tuning the microfluidic cavity modes to the different IR vibrations of the trimethylated benzene, ΔG° either increases or decreases depending only on the symmetry of the normal mode that is coupled. This result reveals the critical role of symmetry in VSC and, in turn, provides an explanation for why the magnitude of chemical changes induced by VSC are much greater than the Rabi splitting, that is, the energy perturbation caused by VSC. These findings further confirm that VSC is powerful and versatile tool for the molecular sciences.Entities:
Keywords: charge transfer; light-matter strong coupling; polaritonic chemistry; symmetry; vibrations
Year: 2020 PMID: 32220038 DOI: 10.1002/anie.202002527
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336