Nicholas A. Lau
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
Deborin Ghosh
Dr Susannah Bourne-Worster susannah.l.bourne-worster@durham.ac.uk
Assistant Professor
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 |
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