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Unraveling the Ultrafast Photochemical Dynamics of Nitrobenzene in Aqueous Solution

Lau, Nicholas A.; Ghosh, Deborin; Bourne-Worster, Susannah; Kumar, Rhea; Whitaker, William A.; Heitland, Jonas; Davies, Julia A.; Karras, Gabriel; Clark, Ian P.; Greetham, Gregory M.; Worth, Graham A.; Orr-Ewing, Andrew J.; Fielding, Helen H.

Authors

Nicholas A. Lau

Deborin Ghosh

Rhea Kumar

William A. Whitaker

Jonas Heitland

Julia A. Davies

Gabriel Karras

Ian P. Clark

Gregory M. Greetham

Graham A. Worth

Andrew J. Orr-Ewing

Helen H. Fielding



Abstract

Nitroaromatic compounds are major constituents of the brown carbon aerosol particles in the troposphere that absorb near-ultraviolet (UV) and visible solar radiation and have a profound effect on the Earth’s climate. The primary sources of brown carbon include biomass burning, forest fires, and residential burning of biofuels, and an important secondary source is photochemistry in aqueous cloud and fog droplets. Nitrobenzene is the smallest nitroaromatic molecule and a model for the photochemical behavior of larger nitroaromatic compounds. Despite the obvious importance of its droplet photochemistry to the atmospheric environment, there have not been any detailed studies of the ultrafast photochemical dynamics of nitrobenzene in aqueous solution. Here, we combine femtosecond transient absorption spectroscopy, time-resolved infrared spectroscopy, and quantum chemistry calculations to investigate the primary steps following the near-UV (λ ≥ 340 nm) photoexcitation of aqueous nitrobenzene. To understand the role of the surrounding water molecules in the photochemical dynamics of nitrobenzene, we compare the results of these investigations with analogous measurements in solutions of methanol, acetonitrile, and cyclohexane. We find that vibrational energy transfer to the aqueous environment quenches internal excitation, and therefore, unlike the gas phase, we do not observe any evidence for formation of photoproducts on timescales up to 500 ns. We also find that hydrogen bonding between nitrobenzene and surrounding water molecules slows the S1/S0 internal conversion process.

Citation

Lau, N. A., Ghosh, D., Bourne-Worster, S., Kumar, R., Whitaker, W. A., Heitland, J., Davies, J. A., Karras, G., Clark, I. P., Greetham, G. M., Worth, G. A., Orr-Ewing, A. J., & Fielding, H. H. (2024). Unraveling the Ultrafast Photochemical Dynamics of Nitrobenzene in Aqueous Solution. Journal of the American Chemical Society, 146(15), 10407-10417. https://doi.org/10.1021/jacs.3c13826

Journal Article Type Article
Acceptance Date Mar 11, 2024
Online Publication Date Apr 4, 2024
Publication Date Apr 17, 2024
Deposit Date Jan 27, 2025
Journal Journal of the American Chemical Society
Print ISSN 0002-7863
Electronic ISSN 1520-5126
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 146
Issue 15
Pages 10407-10417
DOI https://doi.org/10.1021/jacs.3c13826
Public URL https://durham-repository.worktribe.com/output/3353277
Publisher URL https://pubs.acs.org/doi/full/10.1021/jacs.3c13826