Signatures in Vibrational and Vibronic Spectra of Benzene Molecular Clusters

The photoabsorption and infrared spectra (IR) of molecular systems are heavily influenced by aggregation. In the electronic spectra, the vibronic coupling effect is of utmost importance. Although treating both effects simultaneously can be challenging, it is often the only way to explain the experimental spectrum of molecular clusters. In this work, we study IR spectra and the vibronic coupling effect in the electronic photoabsorption spectra in molecular systems composed of benzene (monomer, dimers, and crystal). Photoabsorption spectra were generated using the direct vibronic coupling method at the density functional theory (DFT) level. We also simulated the spectra with the Liouville-Lanczos approach by calculating the electronic transitions along the main inducing modes for two forbidden transitions (<sup>1</sup>A<sub>1g</sub> → <sup>1</sup>B<sub>2u</sub> and <sup>1</sup>A<sub>1g</sub> → <sup>1</sup>B<sub>1u</sub>). DFT was also applied to simulate IR spectra. For the monomer, vibronic coupling was crucial to induce the first and second forbidden transitions. On the other hand, molecular aggregation was sufficient to induce the first and second forbidden transitions in almost all dimers. However, when the vibronic coupling is evaluated for the clusters, the band in the energy range of the <sup>1</sup>A<sub>1g</sub> → <sup>1</sup>B<sub>1u</sub> transition is affected both by the aggregation itself and the inducing modes. Moreover, some inducing modes drastically change the allowed <sup>1</sup>A<sub>1g</sub> → <sup>1</sup>E<sub>1u</sub> transition, depending on the dimer under study due to symmetry breaking. In terms of IR spectra, clear signatures are present. For instance, the intensities of the C-H stretching modes decrease as aggregation increases. This work shows that aggregation impacts the band shapes differently in relation to the benzene aggregate structure and the excitation under analysis.

Authors

Institutions

Publication Details

Journal
The Journal of Physical Chemistry A
Published
2025-04-09
DOI
https://doi.org/10.1021/acs.jpca.4c08700
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
0.00

Funders

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

Signatures in Vibrational and Vibronic Spectra of Benzene Molecular Clusters

Alexandre B. Rocha, Ricardo R. Oliveira, Amanda D. Torres, Ricardo Montserrat
The Journal of Physical Chemistry A
Advanced Chemical Physics Studies
article

Signatures in Vibrational and Vibronic Spectra of Benzene Molecular Clusters

Alexandre B. Rocha, Ricardo R. Oliveira, Amanda D. Torres, Ricardo Montserrat
article en

Abstract

The photoabsorption and infrared spectra (IR) of molecular systems are heavily influenced by aggregation. In the electronic spectra, the vibronic coupling effect is of utmost importance. Although treating both effects simultaneously can be challenging, it is often the only way to explain the experimental spectrum of molecular clusters. In this work, we study IR spectra and the vibronic coupling effect in the electronic photoabsorption spectra in molecular systems composed of benzene (monomer, dimers, and crystal). Photoabsorption spectra were generated using the direct vibronic coupling method at the density functional theory (DFT) level. We also simulated the spectra with the Liouville-Lanczos approach by calculating the electronic transitions along the main inducing modes for two forbidden transitions (<sup>1</sup>A<sub>1g</sub> → <sup>1</sup>B<sub>2u</sub> and <sup>1</sup>A<sub>1g</sub> → <sup>1</sup>B<sub>1u</sub>). DFT was also applied to simulate IR spectra. For the monomer, vibronic coupling was crucial to induce the first and second forbidden transitions. On the other hand, molecular aggregation was sufficient to induce the first and second forbidden transitions in almost all dimers. However, when the vibronic coupling is evaluated for the clusters, the band in the energy range of the <sup>1</sup>A<sub>1g</sub> → <sup>1</sup>B<sub>1u</sub> transition is affected both by the aggregation itself and the inducing modes. Moreover, some inducing modes drastically change the allowed <sup>1</sup>A<sub>1g</sub> → <sup>1</sup>E<sub>1u</sub> transition, depending on the dimer under study due to symmetry breaking. In terms of IR spectra, clear signatures are present. For instance, the intensities of the C-H stretching modes decrease as aggregation increases. This work shows that aggregation impacts the band shapes differently in relation to the benzene aggregate structure and the excitation under analysis.

The Journal of Physical Chemistry AVol. 129(15)
Universidade Federal do Rio de Janeiro (BR), Instituto Federal do Paraná (BR)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
Openalex Percentile: Top 94%
Advanced Chemical Physics Studies
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.