A Phenomenological Symmetry Rule for Chemical Reactivity Under Vibrational Strong Coupling

Symmetry is known to strongly influence the course of a chemical reaction. It has also been found to play a key role in vibrational strong coupling (VSC), where it can influence the outcome of chemical reactions or alter chemical equilibria. However, the precise nature of this effect and its extent remains elusive. To further explore the role of vibrational symmetry, we have investigated the equilibrium constants of different charge transfer complexes, in particular of isomers of trimethyl benzene belonging to different point groups from which a general symmetry rule emerges. We describe the strongly coupled system by a direct product of irreducible representations associated with the complexes and the cavity. As a consequence, the coupled vibration is associated with a new irreducible representation that projects differently on the reaction coordinate of the charge transfer complexation, reflecting the changes in the equilibrium constants. This phenomenological symmetry rule points to a general underlying framework for predicting the outcome of chemical reactivity under VSC.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-06-24
DOI
https://doi.org/10.1002/anie.202503915
Citations
3
Primary Topic
Spectroscopy and Quantum Chemical Studies
Type
article
Field-Weighted Citation Impact
3.74

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Phenomenological Symmetry Rule for Chemical Reactivity Under Vibrational Strong Coupling

Kalaivanan Nagarajan, Cyriaque Genet, Yoonsoo Pang, Anjali Jayachandran et al.
3 citations
Angewandte Chemie International Edition
Spectroscopy and Quantum Chemical Studies
3.74
article

A Phenomenological Symmetry Rule for Chemical Reactivity Under Vibrational Strong Coupling

Kalaivanan Nagarajan, Cyriaque Genet, Yoonsoo Pang, Anjali Jayachandran, Bianca Patrahau, Thomas W. Ebbesen, Mukesh Kumar Mahato, A. Thomas, John G. Ricca
article en
3 citations

Abstract

Symmetry is known to strongly influence the course of a chemical reaction. It has also been found to play a key role in vibrational strong coupling (VSC), where it can influence the outcome of chemical reactions or alter chemical equilibria. However, the precise nature of this effect and its extent remains elusive. To further explore the role of vibrational symmetry, we have investigated the equilibrium constants of different charge transfer complexes, in particular of isomers of trimethyl benzene belonging to different point groups from which a general symmetry rule emerges. We describe the strongly coupled system by a direct product of irreducible representations associated with the complexes and the cavity. As a consequence, the coupled vibration is associated with a new irreducible representation that projects differently on the reaction coordinate of the charge transfer complexation, reflecting the changes in the equilibrium constants. This phenomenological symmetry rule points to a general underlying framework for predicting the outcome of chemical reactivity under VSC.

Angewandte Chemie International EditionVol. 64(35)
Tata Institute of Fundamental Research (IN), Centre National de la Recherche Scientifique (FR), Institut de Science et d'Ingénierie Supramoléculaires (FR), Shandong Jianzhu University (CN), Indian Institute of Science Bangalore (IN), Université de Strasbourg (FR)
Agence Nationale de la Recherche
Openalex Percentile: Top 7%
Spectroscopy and Quantum Chemical Studies
3.74
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.